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<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">jsms</journal-id><journal-title-group><journal-title xml:lang="ru">Journal of Siberian Medical Sciences</journal-title><trans-title-group xml:lang="en"><trans-title>Journal of Siberian Medical Sciences</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2542-1174</issn><publisher><publisher-name>Federal state budgetary educational institution of higher education "Novosibirsk state medical university" of  Ministry of Health of the Russian Federation (FSBEI HE NSMU MOH Russia)</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.31549/2542-1174-2021-4-108-133</article-id><article-id custom-type="elpub" pub-id-type="custom">jsms-780</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ОБЗОРЫ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>REVIEW</subject></subj-group></article-categories><title-group><article-title>Аберрантная экспрессия и метилирование генов отдельных микроРНК при лимфопролиферативных заболеваниях: обзор литературы</article-title><trans-title-group xml:lang="en"><trans-title>Aberrant expression and methylation of individual microRNAs genes in lymphoproliferative diseases: a literature review</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Воропаева</surname><given-names>Е. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Voropaeva</surname><given-names>E. N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Воропаева Елена Николаевна — д-р мед. наук, ст. научный сотрудник лаборатории молекулярно-генетических исследований терапевтических заболеваний</p><p>Новосибирск</p></bio><bio xml:lang="en"><p>Elena N. Voropaeva — Dr. Sci. (Med.), Senior Researcher, Laboratory for Molecular Genetic Research of Therapeutic Diseases </p><p>Novosibirsk</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Березина</surname><given-names>О. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Berezina</surname><given-names>O. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Березина Ольга Валерьевна — канд. мед. наук, врач-гематолог, ассистент кафедры терапии, гематологии и трансфузиологии </p></bio><bio xml:lang="en"><p>Olga V. Berezina — Cand. Sci. (Med.), Hematologist, Assistant, Department of Therapy, Hematology and Transfusiology </p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Чуркина</surname><given-names>М. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Churkina</surname><given-names>M. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Чуркина Мария Игоревна  — аспирант кафедры терапии, гематологии и трансфузиологии </p><p>630091, г. Новосибирск, Красный пр., 52</p></bio><bio xml:lang="en"><p>Maria I. Churkina — Post-Graduate Student, Department of Therapy, Hematology and Transfusiology </p><p>52, Krasny Prospect, Novosibirsk, 630091 </p></bio><email xlink:type="simple">nats.sagan@yandex.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Поспелова</surname><given-names>Т. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Pospelova</surname><given-names>T. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Поспелова Татьяна Ивановна — д-р мед. наук, профессор, заведующий кафедрой терапии, гематологии и трансфузиологии  </p></bio><bio xml:lang="en"><p>Tatiana I. Pospelova — Dr. Sci. (Med.), Professor, Head, Department of Therapy, Hematology and Transfusiology </p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Лызлова</surname><given-names>А. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Lyzlova</surname><given-names>A. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Лызлова Арина Андреевна — врач-гематолог </p></bio><bio xml:lang="en"><p>Arina A. Lyzlova — Hematologist </p></bio><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Максимов</surname><given-names>В. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Maksimov</surname><given-names>V. N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Максимов Владимир Николаевич — д-р мед. наук, главный научный сотрудник, заведующий лабораторией молекулярно-генетических исследований терапевтических заболеваний  </p><p>Новосибирск</p></bio><bio xml:lang="en"><p>Vladimir N. Maksimov — Dr. Sci. (Med.), Chief Researcher, Head, Laboratory for Molecular Genetic Research of Therapeutic Diseases </p><p>Novosibirsk</p></bio><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>НИИ терапии и профилактической медицины — филиал ФГБНУ «Федеральный исследовательский центр Институт цитологии и генетики СО РАН»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Institute of Internal and Preventive Medicine</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>ФГБОУ ВО «Новосибирский государственный медицинский университет» Минздрава России</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Novosibirsk State Medical University</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-3"><aff xml:lang="ru"><institution>ГБУЗ НСО «Государственная Новосибирская областная клиническая больница»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>State Novosibirsk Regional Clinical Hospital</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2021</year></pub-date><pub-date pub-type="epub"><day>20</day><month>01</month><year>2022</year></pub-date><volume>0</volume><issue>4</issue><fpage>108</fpage><lpage>133</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Воропаева Е.Н., Березина О.В., Чуркина М.И., Поспелова Т.И., Лызлова А.А., Максимов В.Н., 2022</copyright-statement><copyright-year>2022</copyright-year><copyright-holder xml:lang="ru">Воропаева Е.Н., Березина О.В., Чуркина М.И., Поспелова Т.И., Лызлова А.А., Максимов В.Н.</copyright-holder><copyright-holder xml:lang="en">Voropaeva E.N., Berezina O.V., Churkina M.I., Pospelova T.I., Lyzlova A.A., Maksimov V.N.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://jsms.elpub.ru/jour/article/view/780">https://jsms.elpub.ru/jour/article/view/780</self-uri><abstract><p>В последние десятилетия обнаружено, что микроРНК участвуют практически во всех клеточных процессах, в том числе в развитии опухолей.В представленном обзоре рассмотрена молекулярно-генетическая характеристика ряда микроРНК, функционирующих при нормальном кроветворении, нарушение экспрессии которых показано при развитии лимфопролиферативных заболеваний. Приведены последние опубликованные результаты исследований по диагностическому, прогностическому и клиническому значению метилирования генов рассматриваемых микроРНК при злокачественных новообразованиях системы крови.</p></abstract><trans-abstract xml:lang="en"><p>In recent decades, it has been found that microRNAs are involved in almost all cellular processes, including the development of tumors.In this paper, we consider the molecular genetic characteristics of a number of microRNAs that function in normal hematopoiesis, whose expression is impaired in the development of lymphoproliferative diseases. The last published results of studies on the diagnostic, prognostic and clinical significance of gene methylation considered by microRNAs in malignant neoplasms of the blood system are presented.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>микроРНК</kwd><kwd>гемобластозы</kwd><kwd>метилирование</kwd><kwd>miR-129</kwd><kwd>miR-342</kwd><kwd>miR-196b</kwd><kwd>miR-9</kwd><kwd>miR-126</kwd><kwd>m iR-137</kwd></kwd-group><kwd-group xml:lang="en"><kwd>microRNA</kwd><kwd>hemoblastosis</kwd><kwd>methylation</kwd><kwd>miR-129</kwd><kwd>miR-342</kwd><kwd>miR-196b</kwd><kwd>miR-9</kwd><kwd>miR-126</kwd><kwd>miR-137</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Работа выполнена в рамках бюджетной темы по Государственному заданию № АААА-А17-117112850280-2.</funding-statement><funding-statement xml:lang="en">The work was carried out within the framework of the budgetary theme under the State Assignment No. АААА-А17-117112850280-2.</funding-statement></funding-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Hannafon B.N., Cai A., Calloway C.L. et al. miR-23b and miR-27b are oncogenic microRNAs in breast cancer: evidence from a CRISPR/Cas9 deletion study // BMC Cancer. 2019. Vol. 19: 642. doi: 10.1186/s12885-019-5839-2.</mixed-citation><mixed-citation xml:lang="en">Hannafon B.N., Cai A., Calloway C.L. et al. (2019). miR-23b and miR-27b are oncogenic microRNAs in breast cancer: evidence from a CRISPR/Cas9 deletion study. BMC Cancer, 19, 642. doi: 10.1186/s12885-019-5839-2.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Ambros V., Bartel B., Bartel D.P. et al. A uniform system for microRNA annotation // RNA. 2003. Vol. 9 (3). P. 277–279. doi: 10.1261/rna.2183803.</mixed-citation><mixed-citation xml:lang="en">Ambros V., Bartel B., Bartel D.P. et al. (2003). A uniform system for microRNA annotation. RNA, 9 (3), 277–279. doi: 10.1261/rna.2183803.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Fabian M.R., Sonenberg N., Filipowicz W. Regulation of mRNA translation and stability by microRNAs // Ann. Rev. Biochem. 2010. Vol. 79. P. 351–379. doi: 10.1146/annurev-biochem-060308-103103.</mixed-citation><mixed-citation xml:lang="en">Fabian M.R., Sonenberg N., Filipowicz W. (2010). Regulation of mRNA translation and stability by microRNAs. Ann. Rev. Biochem., 79, 351–379. doi: 10.1146/annurev-biochem-060308-103103.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Аушев В.Н. МикроРНК: малые молекулы с большим значением // Клин. онкогематология. 2015. Т. 8, № 1. С. 1–12.</mixed-citation><mixed-citation xml:lang="en">Aushev V.N. (2015). MicroRNA: small molecules of great significance. Clinical Oncohematology, 8 (1), 1–12.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Musilova K., Mraz M. MicroRNAs in B-cell lymphomas: how a complex biology gets more complex // Leukemia. 2015. Vol. 29 (5). P. 1004–1017. doi: 10.1038/leu.2014.351.</mixed-citation><mixed-citation xml:lang="en">Musilova K., Mraz M. (2015). MicroRNAs in B-cell lymphomas: how a complex biology gets more complex. Leukemia, 29 (5), 1004–1017. doi: 10.1038/leu.2014.351.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">O’Connell R.M., Baltimore D. MicroRNAs and hematopoietic cell development // Curr. Top. Dev. Biol. 2012. Vol. 99. P. 145–174. doi: 10.1016/B978-0-12-387038-4.00006-9.</mixed-citation><mixed-citation xml:lang="en">O’Connell R.M., Baltimore D. (2012). MicroRNAs and hematopoietic cell development. Curr. Top. Dev. Biol., 99, 145–174. doi: 10.1016/B978-0-12-387038- 4.00006-9.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Mazan-Mamczarz K., Gartenhaus R.B. Role of microRNA deregulation in the pathogenesis of diffuse large B-cell lymphoma (DLBCL) // Leuk. Res. 2013. Vol. 37 (11). P. 1420–1428. doi: 10.1016/j.leukres.2013.08.020.</mixed-citation><mixed-citation xml:lang="en">Mazan-Mamczarz K., Gartenhaus R.B. (2013). Role of microRNA deregulation in the pathogenesis of diffuse large B-cell lymphoma (DLBCL). Leuk. Res., 37 (11), 1420–1428. doi: 10.1016/j.leukres.2013.08.020.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Chen X., Hu H., Guan X. et al. CpG island methylation status of miRNAs in esophageal squamous cell carcinoma // Int. J. Cancer. 2012. Vol. 130 (7). P. 1607– 1613. doi: 10.1002/ijc.26171.</mixed-citation><mixed-citation xml:lang="en">Chen X., Hu H., Guan X. et al. (2012). CpG island methylation status of miRNAs in esophageal squamous cell carcinoma. Int. J. Cancer, 130 (7), 1607– 1613. doi: 10.1002/ijc.26171.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Wong K.Y., Yim R.L.H., Kwong Y.L. et al. Epigenetic inactivation of the MIR129-2 in hematological malignancies // J. Hematol. Oncol. 2013. Vol. 6: 16. doi: 10.1186/1756-8722-6-16.</mixed-citation><mixed-citation xml:lang="en">Wong K.Y., Yim R.L.H., Kwong Y.L. et al. (2013). Epigenetic inactivation of the MIR129-2 in hematological malignancies. J. Hematol. Oncol., 6, 16. doi: 10.1186/1756-8722-6-16.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Baylin S.B., Jones P.A. Epigenetic determinants of cancer // Cold Spring Harb. Perspect. Biol. 2016. Vol. 8 (9): a019505. doi: 10.1101/cshperspect.a019505.</mixed-citation><mixed-citation xml:lang="en">Baylin S.B., Jones P.A. (2016). Epigenetic determinants of cancer. Cold Spring Harb. Perspect. Biol., 8 (9), a019505. doi: 10.1101/cshperspect.a019505.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Yang J., Sun G., Hu Y. et al. Extracellular vesicle lncRNA metastasis-associated lung adenocarcinoma transcript 1 released from glioma stem cells modulates the inflammatory response of microglia after lipopolysaccharide stimulation through regulating miR-129-5p/high mobility group box-1 protein axis // Front. Immunol. 2020. Vol. 10: 3161. doi: 10.3389/fimmu.2019.03161.</mixed-citation><mixed-citation xml:lang="en">Yang J., Sun G., Hu Y. et al. (2020). Extracellular vesicle lncRNA metastasis-associated lung adenocarcinoma transcript 1 released from glioma stem cells modulates the inflammatory response of microglia after lipopolysaccharide stimulation through regulating miR-129-5p/high mobility group box-1 protein axis. Front. Immunol., 10, 3161. doi: 10.3389/fimmu.2019.03161.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">He Y., Huang C., Zhang L., Li J. Epigenetic repression of miR-129-2 in cancer // Liver Int. 2014. Vol. 34 (4): 646. doi: 10.1111/liv.12367.</mixed-citation><mixed-citation xml:lang="en">He Y., Huang C., Zhang L., Li J. (2014). Epigenetic repression of miR-129-2 in cancer. Liver Int., 34 (4), 646. doi: 10.1111/liv.12367.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Пронина И.В., Климов Е.А., Бурденный А.М. и др. Метилирование генов микроРНК miR-129-2, miR-9-1, изменение их экспрессии и активация генов потенциальных мишеней этих микроРНК при раке почки // Молекулярная биология. 2017. T. 51, № 1. C. 73–84.</mixed-citation><mixed-citation xml:lang="en">Pronina I.V., Klimov E.A., Burdennyj A.M. et al. (2017). Methylation of the genes for the microRNAs miR-129-2 and miR-9-1, changes in their expression, and activation of their potential target genes in clear cell renal cell carcinoma. Molecular Biology, 51 (1), 73–84.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Daniunaite K., Dubikaityte M., Gibas P. et al. Clinical significance of miRNA host gene promoter methylation in prostate cancer // Hum. Mol. Genet. 2017. Vol. 26 (13). P. 2451–2461. doi: 10.1093/hmg/ddx138.</mixed-citation><mixed-citation xml:lang="en">Daniunaite K., Dubikaityte M., Gibas P. et al. (2017). Clinical significance of miRNA host gene promoter methylation in prostate cancer. Hum. Mol. Genet., 26 (13), 2451–2461. doi: 10.1093/hmg/ddx138.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Tian Y.X., Zhang L., Sun L.G., Li M. Epigenetic regulation of miR-129-2 leads to overexpression of PDGFRa and FoxP1 in glioma cells // Asian Pac. J. Cancer Prev. 2015. Vol. 16 (14). P. 6129–6133. doi: 10.7314/apjcp.2015.16.14.6129.</mixed-citation><mixed-citation xml:lang="en">Tian Y.X., Zhang L., Sun L.G., Li M. (2015). Epigenetic regulation of miR-129-2 leads to overexpression of PDGFRa and FoxP1 in glioma cells. Asian Pac. J. Cancer Prev., 16 (14), 6129–6133. doi: 10.7314/apjcp.2015.16.14.6129.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Deng B., Tang X., Wang Y. (2021). Role of microRNA-129 in cancer and non-cancerous diseases. Exp. Ther. Med., 22 (3), 918. doi: 10.3892/etm.2021.10350.</mixed-citation><mixed-citation xml:lang="en">Deng B., Tang X., Wang Y. (2021). Role of microRNA-129 in cancer and non-cancerous diseases. Exp Ther. Med., 22 (3), 918. doi: 10.3892/etm.2021.10350.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Torres-Ferreira J., Ramalho-Carvalho J., Gomez A. et al. MiR-193b promoter methylation accurately detects prostate cancer in urine sediments and miR-34b/c or miR-129-2 promoter methylation define subsets of clinically aggressive tumors // Mol. Cancer. 2017. Vol. 16 (1): 26. doi: 10.1186/s12943-017-0604-0.</mixed-citation><mixed-citation xml:lang="en">Torres-Ferreira J., Ramalho-Carvalho J., Gomez A. et al. (2017). MiR-193b promoter methylation accurately detects prostate cancer in urine sediments and miR-34b/c or miR-129-2 promoter methylation define subsets of clinically aggressive tumors. Mol. Cancer, 16 (1), 26. doi: 10.1186/s12943-017-0604-0.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Heydarzadeh S., Ranjbar M., Karimi F., Seif F., Alivand M.R. Overview of host miRNA properties and their association with epigenetics, long non-coding RNAs, and Xeno-infectious factors // Cell. Biosci. 2021. Vol. 11 (1): 43. doi: 10.1186/s13578-021-00552-1.</mixed-citation><mixed-citation xml:lang="en">Heydarzadeh S., Ranjbar M., Karimi F., Seif F., Alivand M.R. (2021). Overview of host miRNA properties and their association with epigenetics, long non-coding RNAs, and Xeno-infectious factors. Cell. Biosci., 11 (1), 43. doi: 10.1186/s13578-021-00552-1.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Tsai K.W., Wu C.W., Hu L.Y. et al. Epigenetic regulation of miR-34b and miR-129 expression in gastric cancer // Int. J. Cancer. 2011. Vol. 129 (11). P. 2600–2610. doi: 10.1002/ijc.25919.</mixed-citation><mixed-citation xml:lang="en">Tsai K.W., Wu C.W., Hu L.Y. et al. (2011). Epigenetic regulation of miR-34b and miR-129 expression in gastric cancer. Int. J. Cancer, 129 (11), 2600–2610. doi: 10.1002/ijc.25919.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Gebhardt K., Edemir B., Groß E. et al. BRAF/EZH2 signaling represses miR-129-5p inhibition of SOX4 thereby modulating BRAFi resistance in melanoma // Cancers (Basel). 2021. Vol. 13 (10): 2393. doi: 10.3390/cancers13102393.</mixed-citation><mixed-citation xml:lang="en">Gebhardt K., Edemir B., Groß E. et al. (2021). BRAF/ EZH2 signaling represses miR-129-5p inhibition of SOX4 thereby modulating BRAFi resistance in melanoma. Cancers (Basel), 13 (10), 2393. doi: 10.3390/cancers13102393.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Koens L., Qin Y., Leung W.Y. et al. MicroRNA profiling of primary cutaneous large B-cell lymphomas // PLoS One. 2013. Vol. 8 (12): e82471. doi: 10.1371/journal.pone.0082471.</mixed-citation><mixed-citation xml:lang="en">Koens L., Qin Y., Leung W.Y. et al. (2013). MicroRNA profiling of primary cutaneous large B-cell lymphomas. PLoS One, 8 (12), e82471. doi: 10.1371/journal.pone.0082471.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Mei M., Wang Y., Wang Q. et al. CircCDYL serves as a new biomarker in mantle cell lymphoma and promotes cell proliferation // Cancer Manag. Res. 2019. Vol. 11. P. 10215–10221. doi: 10.2147/CMAR.S232075.</mixed-citation><mixed-citation xml:lang="en">Mei M., Wang Y., Wang Q. et al. (2019). CircCDYL serves as a new biomarker in mantle cell lymphoma and promotes cell proliferation. Cancer Manag. Res., 11, 10215–10221. doi: 10.2147/CMAR.S232075.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Kim D., Nguyen Q.T., Lee J. et al. Anti-inflammatory roles of glucocorticoids are mediated by Foxp3+ regulatory T cells via a miR-342-dependent mechanism // Immunity. 2020. Vol. 53 (3). P. 581–596. doi: 10.1016/j.immuni.2020.07.002.</mixed-citation><mixed-citation xml:lang="en">Kim D., Nguyen Q.T., Lee J. et al. (2020). Antiinflammatory roles of glucocorticoids are mediated by Foxp3+ regulatory T cells via a miR-342-dependent mechanism. Immunity, 53 (3), 581–596. doi: 10.1016/j.immuni.2020.07.002.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Wang H., Wu J., Meng X. et al. MicroRNA-342 inhibits colorectal cancer cell proliferation and invasion by directly targeting DNA methyltransferase // Carcinogenesis. 2011. Vol. 32 (7). P. 1033–1042. doi: 10.1093/carcin/bgr081.</mixed-citation><mixed-citation xml:lang="en">Wang H., Wu J., Meng X. et al. (2011). MicroRNA-342 inhibits colorectal cancer cell proliferation and invasion by directly targeting DNA methyltransferase. Carcinogenesis, 32 (7), 1033–1042. doi: 10.1093/carcin/bgr081.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Tai M.C., Kajino T., Nakatochi M. et al. miR-342-3p regulates MYC transcriptional activity via direct repression of E2F1 in human lung cancer // Carcinogenesis. 2015. Vol. 36 (12). P. 1464–1473. doi: 10.1093/carcin/bgv152.</mixed-citation><mixed-citation xml:lang="en">Tai M.C., Kajino T., Nakatochi M. et al. (2015). MiR- 342-3p regulates MYC transcriptional activity via direct repression of E2F1 in human lung cancer. Carcinogenesis, 36 (12), 1464–1473. doi: 10.1093/carcin/bgv152.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Gowda P.S., Wildman B.J., Trotter T.N. et al. Run x2 suppression by miR-342 and miR-363 inhibits multiple myeloma progression // Mol. Cancer Res. 2018. Vol. 16 (7). P. 1138–1148. doi: 10.1158/1541-7786.MCR-17-0606.</mixed-citation><mixed-citation xml:lang="en">Gowda P.S., Wildman B.J., Trotter T.N. et al. (2018). Run x2 suppression by miR-342 and miR-363 inhibits multiple myeloma progression. Mol. Cancer Res., 16 (7), 1138–1148. doi: 10.1158/1541-7786.MCR-17-0606.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Weng W., Okugawa Y., Toden S. et al. FOXM1 and FOXQ1 are promising prognostic biomarkers and novel targets of tumor-suppressive miR-342 in human colorectal cancer // Clin. Cancer Res. 2016. Vol. 22 (19). P. 4947–4957. doi: 10.1158/1078-0432.CCR-16-0360.</mixed-citation><mixed-citation xml:lang="en">Weng W., Okugawa Y., Toden S. et al. (2016). FOXM1 and FOXQ1 are promising prognostic biomarkers and novel targets of tumor-suppressive miR-342 in human colorectal cancer. Clin. Cancer Res., 22 (19), 4947–4957. doi: 10.1158/1078-0432.CCR-16-0360.</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Li Z., Wong K.Y., Chan G.C., Chng W.J., Chim C.S. Epigenetic silencing of EVL/miR-342 in multiple myeloma // Transl. Res. 2018. Vol. 192. P. 46–53. doi: 10.1016/j.trsl.2017.11.005.</mixed-citation><mixed-citation xml:lang="en">Li Z., Wong K.Y., Chan G.C., Chng W.J., Chim C.S. (2018). Epigenetic silencing of EVL/miR-342 in multiple myeloma. Transl. Res., 192, 46–53. doi: 10.1016/j.trsl.2017.11.005.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Bai Y., Li Y., Bai J., Zhang Y. Hsa_circ_0004674 promotes osteosarcoma doxorubicin resistance by regulating the miR-342-3p/FBN1 axis // J. Orthop. Surg. Res. 2021. Vol. 16 (1): 510. doi: 10.1186/s13018-021-02631-y.</mixed-citation><mixed-citation xml:lang="en">Bai Y., Li Y., Bai J., Zhang Y. (2021). Hsa_ circ_0004674 promotes osteosarcoma doxorubicin resistance by regulating the miR-342-3p/FBN1 axis. J. Orthop. Surg. Res., 16 (1), 510. doi: 10.1186/s13018-021-02631-y.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Veys C., Benmoussa A., Contentin R. et al. Tumor suppressive role of miR-342-5p in human chondrosarcoma cells and 3D organoids // Int. J. Mol. Sci. 2021. Vol. 22 (11): 5590. doi: 10.3390/ijms22115590.</mixed-citation><mixed-citation xml:lang="en">Veys C., Benmoussa A., Contentin R. et al. (2021). Tumor suppressive role of miR-342-5p in human chondrosarcoma cells and 3D organoids. Int. J. Mol. Sci., 22 (11), 5590. doi: 10.3390/ijms22115590.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Romero-Cordoba S.L., Rodriguez-Cuevas S., BautistaPina V. et al. Loss of function of miR-342-3p results in MCT1 over-expression and contributes to oncogenic metabolic reprogramming in triple negative breast cancer // Sci. Rep. 2018. Vol. 8 (1): 12252. doi: 10.1038/s41598-018-29708-9.</mixed-citation><mixed-citation xml:lang="en">Romero-Cordoba S.L., Rodriguez-Cuevas S., BautistaPina V. et al. (2018). Loss of function of miR-342-3p results in MCT1 over-expression and contributes to oncogenic metabolic reprogramming in triple negative breast cancer. Sci. Rep., 8 (1), 12252. doi: 10.1038/s41598-018-29708-9.</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Ghafouri-Fard S., Dashti S., Farsi M., Hussen B.M., Taheri M. A review on the role of oncogenic lncRNA OIP5-AS1 in human malignancies // Biomed. Pharmacother. 2021. Vol. 137: 111366. doi: 10.1016/j.biopha.2021.111366.</mixed-citation><mixed-citation xml:lang="en">Ghafouri-Fard S., Dashti S., Farsi M., Hussen B.M., Taheri M. (2021). A review on the role of oncogenic lncRNA OIP5-AS1 in human malignancies. Biomed. Pharmacother., 137, 111366. doi: 10.1016/j.biopha.2021.111366.</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Chen Z., Ying J., Shang W. et al. miR-342-3p regulates the proliferation and apoptosis of NSCLC cells by targeting BCL-2 // Technol. Cancer Res. Treat. 2021. Vol. 20: 15330338211041193. doi: 10.1177/15330338211041193.</mixed-citation><mixed-citation xml:lang="en">Chen Z., Ying J., Shang W. et al. (2021). miR- 342-3p regulates the proliferation and apoptosis of NSCLC cells by targeting BCL-2. Technol. Cancer Res. Treat., 20, 15330338211041193. doi: 10.1177/15330338211041193.</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Zhou L., Li J., Tang Y., Yang M. Exosomal LncRNA LINC00659 transferred from cancer-associated fibroblasts promotes colorectal cancer cell progression via miR-342-3p/ANXA2 axis // J. Transl. Med. 2021. Vol. 19 (1): 8. doi: 10.1186/s12967-020-02648-7.</mixed-citation><mixed-citation xml:lang="en">Zhou L., Li J., Tang Y., Yang M. (2021). Exosomal LncRNA LINC00659 transferred from cancer-associated fibroblasts promotes colorectal cancer cell progression via miR-342-3p/ANXA2 axis. J. Transl. Med., 19 (1), 8. doi: 10.1186/s12967-020-02648-7.</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Wang J., Yang Y., Cao Y., Tang X. miR-342 inhibits glioma cell proliferation by targeting GPRC5A // Mol. Med. Rep. 2019. Vol. 20 (1). P. 252–260. doi: 10.3892/mmr.2019.10242.</mixed-citation><mixed-citation xml:lang="en">Wang J., Yang Y., Cao Y., Tang X. (2019). miR- 342 inhibits glioma cell proliferation by targeting GPRC5A. Mol. Med. Rep., 20 (1), 252–260. doi: 10.3892/mmr.2019.10242.</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Young J., Kawaguchi T., Yan L. et al. Tamoxifen sensitivity-related microRNA-342 is a useful biomarker for breast cancer survival // Oncotarget. 2017. Vol. 8 (59). P. 99978–99989. doi: 10.18632/oncotarget.21577.</mixed-citation><mixed-citation xml:lang="en">Young J., Kawaguchi T., Yan L. et al. (2017). Tamoxifen sensitivity-related microRNA-342 is a useful biomarker for breast cancer survival. Oncotarget, 8 (59), 99978–99989. doi: 10.18632/oncotarget.21577.</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Li X.R., Chu H.J., Lu T. et al. miR-342-3p suppresses proliferation, migration and invasion by targeting FOXM1 in human cervical cancer // FEBS Lett. 2014. Vol. 588 (17). P. 3298–3307. doi: 10.1016/j.febslet.2014.07.020.</mixed-citation><mixed-citation xml:lang="en">Li X.R., Chu H.J., Lu T. et al. (2014). miR-342-3p suppresses proliferation, migration and invasion by targeting FOXM1 in human cervical cancer. FEBS Lett., 588 (17), 3298–3307. doi: 10.1016/j.febslet.2014.07.020.</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Zhang M.Y., Calin G.A., Yuen K.S., Jin D.Y., Chim C.S. Epigenetic silencing of miR-342-3p in B cell lymphoma and its impact on autophagy // Clin. Epigenetics. 2020. Vol. 12 (1): 150. doi: 10.1186/s13148-020-00926-1.</mixed-citation><mixed-citation xml:lang="en">Zhang M.Y., Calin G.A., Yuen K.S., Jin D.Y., Chim C.S. (2020). Epigenetic silencing of miR-342-3p in B cell lymphoma and its impact on autophagy. Clin. Epigenetics, 12 (1), 150. doi: 10.1186/s13148-020-00926-1.</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Kersy O., Salmon-Divon M., Shpilberg O., Hershkovitz-Rokah O. Non-coding RNAs in normal B-cell development and in mantle cell lymphoma: from molecular mechanism to biomarker and therapeutic agent potential // Int. J. Mol. Sci. 2021. Vol. 22 (17): 9490. doi: 10.3390/ijms22179490.</mixed-citation><mixed-citation xml:lang="en">Kersy O., Salmon-Divon M., Shpilberg O., Hershkovitz-Rokah O. (2021). Non-coding RNAs in normal B-cell development and in mantle cell lymphoma: from molecular mechanism to biomarker and therapeutic agent potential. Int. J. Mol. Sci., 22 (17), 9490. doi: 10.3390/ijms22179490.</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Mo J.S., Park Y.R., Chae S.C. MicroRNA 196B regulates HOXA5, HOXB6 and GLTP expression levels in colorectal cancer cells // Pathol. Oncol. Res. 2019. Vol. 25 (3). P. 953–959. doi: 10.1007/s12253-018-0399-3.</mixed-citation><mixed-citation xml:lang="en">Mo J.S., Park Y.R., Chae S.C. (2019). MicroRNA 196B regulates HOXA5, HOXB6 and GLTP expression levels in colorectal cancer cells. Pathol. Oncol. Res., 25 (3), 953–959. doi: 10.1007/s12253-018-0399-3.</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Li Z., Huang H., Chen P. et al. Publisher correction: miR-196b directly targets both HOXA9/MEIS1 oncogenes and FAS tumour suppressor in MLL-rearranged leukaemia // Nat. Commun. 2018. Vol. 9: 16192. doi: 10.1038/ncomms16192.</mixed-citation><mixed-citation xml:lang="en">Li Z., Huang H., Chen P. et al. (2018). Publisher correction: miR-196b directly targets both HOXA9/ MEIS1 oncogenes and FAS tumour suppressor in MLL-rearranged leukaemia. Nat. Commun., 9, 16192. doi: 10.1038/ncomms16192.</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Hou Y.Y., You J.J., Yang C.M. et al. Aberrant DNA hypomethylation of miR-196b contributes to migration and invasion of oral cancer // Oncol. Lett. 2016. Vol. 11 (6). P. 4013–4021. doi: 10.3892/ol.2016.4491.</mixed-citation><mixed-citation xml:lang="en">Hou Y.Y., You J.J., Yang C.M. et al. (2016). Aberrant DNA hypomethylation of miR-196b contributes to migration and invasion of oral cancer. Oncol. Lett., 11 (6), 4013–4021. doi: 10.3892/ol.2016.4491.</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Bhatia S., Kaul D., Varma N. Potential tumor suppressive function of miR-196b in B-cell lineage acute lymphoblastic leukemia // Mol. Cell Biochem. 2010. Vol. 340 (1–2). P. 97–106. doi: 10.1007/s11010-010-0406-9.</mixed-citation><mixed-citation xml:lang="en">Bhatia S., Kaul D., Varma N. (2010). Potential tumor suppressive function of miR-196b in B-cell lineage acute lymphoblastic leukemia. Mol. Cell Biochem., 340 (1–2), 97–106. doi: 10.1007/s11010-010-0406-9.</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Tellez C.S., Juri D.E., Do K. et al. miR-196b is epigenetically silenced during the premalignant stage of lung carcinogenesis // Cancer Res. 2016. Vol. 76 (16). P. 4741–4751. doi: 10.1158/0008-5472.CAN-15-3367.</mixed-citation><mixed-citation xml:lang="en">Tellez C.S., Juri D.E., Do K. et al. (2016). miR-196b is epigenetically silenced during the premalignant stage of lung carcinogenesis. Cancer Res., 76 (16), 4741– 4751. doi: 10.1158/0008-5472.CAN-15-3367.</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Kanno S., Nosho K., Ishigami K. et al. MicroRNA-196b is an independent prognostic biomarker in patients with pancreatic cancer // Carcinogenesis. 2017. Vol. 38 (4). P. 425–431. doi: 10.1093/carcin/bgx013.</mixed-citation><mixed-citation xml:lang="en">Kanno S., Nosho K., Ishigami K. et al. (2017). MicroRNA-196b is an independent prognostic biomarker in patients with pancreatic cancer. Carcinogenesis, 38 (4), 425–431. doi: 10.1093/carcin/bgx013.</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Abe W., Nasu K., Nakada C. et al. miR-196b targets c-myc and Bcl-2 expression, inhibits proliferation and induces apoptosis in endometriotic stromal cells // Hum. Rep. 2013. Vol. 28. P. 750–761. doi: 10.1093/humrep/des446.</mixed-citation><mixed-citation xml:lang="en">Abe W., Nasu K., Nakada C. et al. (2013). miR-196b targets c-myc and Bcl-2 expression, inhibits proliferation and induces apoptosis in endometriotic stromal cells. Hum. Rep., 28, 750–761. doi: 10.1093/humrep/des446.</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">Chen C., Zhang Y., Zhang L., Weakley S.M., Yao Q. MicroRNA-196: critical roles and clinical applications in development and cancer // J. Cell. Mol. Med. 2011. Vol. 15 (1). P. 14–23. doi: 10.1111/j.1582-4934.2010.01219.x.</mixed-citation><mixed-citation xml:lang="en">Chen C., Zhang Y., Zhang L., Weakley S.M., Yao Q. (2011). MicroRNA-196: critical roles and clinical applications in development and cancer. J. Cell. Mol. Med., 15 (1), 14–23. doi: 10.1111/j.1582-4934.2010.01219.x.</mixed-citation></citation-alternatives></ref><ref id="cit48"><label>48</label><citation-alternatives><mixed-citation xml:lang="ru">Li Y., Li J., Liu Z., Zhang Y. High expression of miR-196b predicts poor prognosis in patients with ovarian cancer // Onco Targets Ther. 2020. Vol. 13. P. 9797–9806. doi: 10.2147/OTT.S254942.</mixed-citation><mixed-citation xml:lang="en">Li Y., Li J., Liu Z., Zhang Y. (2020). High expression of miR-196b predicts poor prognosis in patients with ovarian cancer. Onco Targets Ther., 13, 9797–9806. doi: 10.2147/OTT.S254942.</mixed-citation></citation-alternatives></ref><ref id="cit49"><label>49</label><citation-alternatives><mixed-citation xml:lang="ru">Wei H., Zhang J., Tan K. et al. Benzene-induced aberrant miRNA expression profile in hematopoietic progenitor cells in C57BL/6 mice // Int. J. Mol. Sci. 2015. Vol. 16 (11). P. 27058–27071. doi: 10.3390/ijms161126001.</mixed-citation><mixed-citation xml:lang="en">Wei H., Zhang J., Tan K. et al. (2015). Benzene-induced aberrant miRNA expression profile in hematopoietic progenitor cells in C57BL/6 mice. Int. J. Mol. Sci., 16 (11), 27058–27071. doi: 10.3390/ijms161126001.</mixed-citation></citation-alternatives></ref><ref id="cit50"><label>50</label><citation-alternatives><mixed-citation xml:lang="ru">Li Z., Huang H., Chen P. et al. miR-196b directly targets both HOXA9/MEIS1 oncogenes and FAS tumour suppressor in MLL-rearranged leukaemia // Nat. Com. 2012. Vol. 3: 688. doi: 10.1038/ncomms1681.</mixed-citation><mixed-citation xml:lang="en">Li Z., Huang H., Chen P. et al. (2012). miR-196b directly targets both HOXA9/MEIS1 oncogenes and FAS tumour suppressor in MLL-rearranged leukaemia. Nat. Com., 3, 688. doi: 10.1038/ncomms1681.</mixed-citation></citation-alternatives></ref><ref id="cit51"><label>51</label><citation-alternatives><mixed-citation xml:lang="ru">Visani M., Marucci G., de Biase D. et al. miR-196B-5P and miR-200B-3P are differentially expressed in medulloblastomas of adults and children // Diagnostics (Basel). 2021. Vol. 11 (9): 1633. doi: 10.3390/diagnostics11091633.</mixed-citation><mixed-citation xml:lang="en">Visani M., Marucci G., de Biase D. et al. (2021). miR-196B-5P and miR-200B-3P are differentially expressed in medulloblastomas of adults and children. Diagnostics (Basel), 11 (9), 1633. doi: 10.3390/diagnostics11091633.</mixed-citation></citation-alternatives></ref><ref id="cit52"><label>52</label><citation-alternatives><mixed-citation xml:lang="ru">Cheng A.J., You G.R., Lee C.J. et al. Systemic investigation identifying salivary miR-196b as a promising biomarker for early detection of head-neck cancer and oral precancer lesions // Diagnostics (Basel). 2021. Vol. 11 (8): 1411. doi: 10.3390/diagnostics11081411.</mixed-citation><mixed-citation xml:lang="en">Cheng A.J., You G.R., Lee C.J. et al. (2021). Systemic investigation identifying salivary miR-196b as a promising biomarker for early detection of head-neck cancer and oral precancer lesions. Diagnostics (Basel), 11 (8), 1411. doi: 10.3390/diagnostics11081411.</mixed-citation></citation-alternatives></ref><ref id="cit53"><label>53</label><citation-alternatives><mixed-citation xml:lang="ru">Shafik R.E., Abd Wahab N., Mokhtar M.M., El Taweel M.A., Ebeid F. Expression of microRNA-181a and microRNA-196b in egyptian pediatric acute lymphoblastic leukemia // Asian Pac. J. Cancer Prev. 2020. Vol. 21 (11). P. 3429–3434. doi: 10.31557/APJCP.2020.21.11.3429.</mixed-citation><mixed-citation xml:lang="en">Shafik R.E., Abd Wahab N., Mokhtar M.M., El Taweel M.A., Ebeid F. (2020). Expression of microRNA-181a and microRNA-196b in egyptian pediatric acute lympho blastic leukemia. Asian Pac. J. Cancer Prev., 21 (11), 3429–3434. doi: 10.31557/APJCP.2020.21.11.3429.</mixed-citation></citation-alternatives></ref><ref id="cit54"><label>54</label><citation-alternatives><mixed-citation xml:lang="ru">Liu Y., Zheng W., Song Y., Ma W., Yin H. Low expression of miR-196b enhances the expression of BCR-ABL1 and HOXA9 oncogenes in chronic myeloid leukemogenesis // PLoS One. 2013. Vol. 8: e68442. doi: 10.1371/journal.pone.0068442.</mixed-citation><mixed-citation xml:lang="en">Liu Y., Zheng W., Song Y., Ma W., Yin H. (2013). Low expression of miR-196b enhances the expression of BCR-ABL1 and HOXA9 oncogenes in chronic myeloid leukemogenesis. PLoS One, 8, e68442. doi: 10.1371/journal.pone.0068442.</mixed-citation></citation-alternatives></ref><ref id="cit55"><label>55</label><citation-alternatives><mixed-citation xml:lang="ru">Schotte D., Lange-Turenhout E.A., Stumpel D.J. et al. Expression of miR-196b is not exclusively MLL-driven but is especially linked to activation of HOXA genes in pediatric acute lymphoblastic leukemia // Haematologica. 2010. Vol. 95 (10). P. 1675–1682. doi: 10.3324/haematol.2010.023481.</mixed-citation><mixed-citation xml:lang="en">Schotte D., Lange-Turenhout E.A., Stumpel D.J. et al. (2010). Expression of miR-196b is not exclusively MLL-driven but is especially linked to activation of HOXA genes in pediatric acute lymphoblastic leukemia. Haematologica, 95 (10), 1675–1682. doi: 10.3324/haematol.2010.023481.</mixed-citation></citation-alternatives></ref><ref id="cit56"><label>56</label><citation-alternatives><mixed-citation xml:lang="ru">Saki N., Abroun S., Soleimani M. et al. Involvement of microRNA in T-cell differentiation and malignancy // Int. J. Hematol. Oncol. Stem. Cell Res. 2015. Vol. 9 (1). P. 33–49.</mixed-citation><mixed-citation xml:lang="en">Saki N., Abroun S., Soleimani M. et al. (2015). Involvement of microRNA in T-cell differentiation and malignancy. Int. J. Hematol. Oncol. Stem. Cell Res., 9 (1), 33–49.</mixed-citation></citation-alternatives></ref><ref id="cit57"><label>57</label><citation-alternatives><mixed-citation xml:lang="ru">Hurtado López A.M., Chen-Liang T.H., Zurdo M. et al. Cancer testis antigens in myelodysplastic syndromes revisited: a targeted RNA-seq approach // Oncoimmunology. 2020. Vol. 9 (1): 1824642. doi: 10.1080/2162402X.2020.1824642.</mixed-citation><mixed-citation xml:lang="en">Hurtado López A.M., Chen-Liang T.H., Zurdo M. et al. (2020). Cancer testis antigens in myelodysplastic syndromes revisited: a targeted RNA-seq approach. Oncoimmunology, 9 (1), 1824642. doi: 10.1080/2162402X.2020.1824642.</mixed-citation></citation-alternatives></ref><ref id="cit58"><label>58</label><citation-alternatives><mixed-citation xml:lang="ru">Dombret H., Seymour J.F., Butrym A. et al. International phase 3 study of azacitidine vs conventional care regimens in older patients with newly diagnosed AML with &gt;30% blasts // Blood. 2015. Vol 126 (3). P. 291–299. doi: 10.1182/blood-2015-01-621664.</mixed-citation><mixed-citation xml:lang="en">Dombret H., Seymour J.F., Butrym A. et al. (2015). International phase 3 study of azacitidine vs conventional care regimens in older patients with newly diagnosed AML with &gt;30% blasts. Blood, 126 (3), 291–299. doi: 10.1182/blood-2015-01-621664.</mixed-citation></citation-alternatives></ref><ref id="cit59"><label>59</label><citation-alternatives><mixed-citation xml:lang="ru">Luan C., Yang Z., Chen B. The functional role of microRNA in acute lymphoblastic leukemia: relevance for diagnosis, differential diagnosis, prognosis, and therapy // Onco Targets Ther. 2015. Vol. 8. P. 2903–2914. doi: 10.2147/OTT.S92470.</mixed-citation><mixed-citation xml:lang="en">Luan C., Yang Z., Chen B. (2015). The functional role of microRNA in acute lymphoblastic leukemia: relevance for diagnosis, differential diagnosis, prognosis, and therapy. Onco Targets Ther., 8, 2903–2914. doi: 10.2147/OTT.S92470.</mixed-citation></citation-alternatives></ref><ref id="cit60"><label>60</label><citation-alternatives><mixed-citation xml:lang="ru">Muraoka T., Soh J., Toyooka S. et al. Impact of aberrant methylation of microRNA-9 family members on non-small cell lung cancers // Mol. Clin. Oncol. 2013. Vol. 1 (1). P. 185–189. doi: 10.3892/mco.2012.18.</mixed-citation><mixed-citation xml:lang="en">Muraoka T., Soh J., Toyooka S. et al. (2013). Impact of aberrant methylation of microRNA-9 family members on non-small cell lung cancers. Mol. Clin. Oncol., 1 (1), 185–189. doi: 10.3892/mco.2012.18.</mixed-citation></citation-alternatives></ref><ref id="cit61"><label>61</label><citation-alternatives><mixed-citation xml:lang="ru">Jia D., Lin W., Tang H. et al. Integrative analysis of DNA methylation and gene expression to identify key epigenetic genes in glioblastoma // Aging (Albany NY). 2019. Vol. 11 (15). P. 5579–5592. doi: 10.18632/aging.102139.</mixed-citation><mixed-citation xml:lang="en">Jia D., Lin W., Tang H. et al. (2019). Integrative analysis of DNA methylation and gene expression to identify key epigenetic genes in glioblastoma. Aging (Albany NY), 11 (15), 5579–5592. doi: 10.18632/aging.102139.</mixed-citation></citation-alternatives></ref><ref id="cit62"><label>62</label><citation-alternatives><mixed-citation xml:lang="ru">Zhang J., Cheng J., Zeng Z. et al. Comprehensive profiling of novel microRNA-9 targets and a tumor suppressor role of microRNA-9 via targeting IGF2BP1 in hepatocellular carcinoma // Oncotarget. 2015. Vol. 6 (39). P. 42040–42052. doi: 10.18632/oncotarget.5969.</mixed-citation><mixed-citation xml:lang="en">Zhang J., Cheng J., Zeng Z. et al. (2015). Comprehensive profiling of novel microRNA-9 targets and a tumor suppressor role of microRNA-9 via targeting IGF2BP1 in hepatocellular carcinoma. Oncotarget., 6 (39), 42040–42052. doi: 10.18632/oncotarget.5969.</mixed-citation></citation-alternatives></ref><ref id="cit63"><label>63</label><citation-alternatives><mixed-citation xml:lang="ru">Zhang J., Jia J., Zhao L. et al. Down-regulation of microRNA-9 leads to activation of IL-6/Jak/STAT3 pathway through directly targeting IL-6 in HeLa cell // Mol. Carcinogen. 2016. Vol. 55 (5). P. 732–742. doi: 10.1002/mc.22317.</mixed-citation><mixed-citation xml:lang="en">Zhang J., Jia J., Zhao L. et al. (2016). Down-regulation of microRNA-9 leads to activation of IL-6/Jak/STAT3 pathway through directly targeting IL-6 in HeLa cell. Mol. Carcinogen., 55 (5), 732–742. doi: 10.1002/mc.22317.</mixed-citation></citation-alternatives></ref><ref id="cit64"><label>64</label><citation-alternatives><mixed-citation xml:lang="ru">Zhu M., Xu Y., Ge M., Gui Z., Yan F. Regulation of UHRF1 by microRNA-9 modulates colorectal cancer cell proliferation and apoptosis // Cancer Sci. 2015. Vol. 106 (7). P. 833–839. doi: 10.1111/cas.12689.</mixed-citation><mixed-citation xml:lang="en">Zhu M., Xu Y., Ge M., Gui Z., Yan F. (2015). Regulation of UHRF1 by microRNA-9 modulates colorectal cancer cell proliferation and apoptosis. Cancer Sci., 106 (7), 833–839. doi: 10.1111/cas.12689.</mixed-citation></citation-alternatives></ref><ref id="cit65"><label>65</label><citation-alternatives><mixed-citation xml:lang="ru">Vrabec K., Boštjančič E., Koritnik B. et al. Differential expression of several miRNAs and the host genes AATK and DNM2 in leukocytes of sporadic ALS patients // Front. Mol. Neurosci. 2018. Vol. 11: 106. doi: 10.3389/fnmol.2018.00106.</mixed-citation><mixed-citation xml:lang="en">Vrabec K., Boštjančič E., Koritnik B. et al. (2018). Differential expression of several miRNAs and the host genes AATK and DNM2 in leukocytes of sporadic ALS patients. Front. Mol. Neurosci., 11, 106. doi: 10.3389/fnmol.2018.00106.</mixed-citation></citation-alternatives></ref><ref id="cit66"><label>66</label><citation-alternatives><mixed-citation xml:lang="ru">Roman-Gomez J., Agirre X., Jiménez-Velasco A. et al. Epigenetic regulation of microRNAs in acute lymphoblastic leukemia // J. Clin. Oncol. 2009. Vol. 27 (8). P. 1316–1322. doi: 10.1200/JCO.2008.19.3441.</mixed-citation><mixed-citation xml:lang="en">Roman-Gomez J., Agirre X., Jiménez-Velasco A. et al. (2009). Epigenetic regulation of microRNAs in acute lymphoblastic leukemia. J. Clin. Oncol., 27 (8), 1316– 1322. doi: 10.1200/JCO.2008.19.3441.</mixed-citation></citation-alternatives></ref><ref id="cit67"><label>67</label><citation-alternatives><mixed-citation xml:lang="ru">Cui Y., Xue Y., Dong S., Zhang P. Plasma microRNA-9 as a diagnostic and prognostic biomarker in patients with esophageal squamous cell carcinoma // J. Int. Med. Res. 2017. Vol. 45 (4). P. 1310–1317. doi: 10.1177/0300060517709370.</mixed-citation><mixed-citation xml:lang="en">Cui Y., Xue Y., Dong S., Zhang P. (2017). Plasma microRNA-9 as a diagnostic and prognostic biomarker in patients with esophageal squamous cell carcinoma. J. Int. Med. Res., 45 (4), 1310–1317. doi: 10.1177/0300060517709370.</mixed-citation></citation-alternatives></ref><ref id="cit68"><label>68</label><citation-alternatives><mixed-citation xml:lang="ru">Mittal N., Li L., Sheng Y. et al. A critical role of epigenetic inactivation of miR-9 in EVI1high pediatric AML // Mol. Cancer. 2019. Vol. 18 (1): 30. doi: 10.1186/s12943-019-0952-z.</mixed-citation><mixed-citation xml:lang="en">Mittal N., Li L., Sheng Y. et al. (2019). A critical role of epigenetic inactivation of miR-9 in EVI1high pediatric AML. Mol. Cancer, 18 (1), 30. doi: 10.1186/s12943-019-0952-z.</mixed-citation></citation-alternatives></ref><ref id="cit69"><label>69</label><citation-alternatives><mixed-citation xml:lang="ru">Rodriguez-Otero P., Román-Gómez J., Vilas-Zornoza A. et al. Deregulation of FGFR1 and CDK6 oncogenic pathways in acute lymphoblastic leukaemia harbouring epigenetic modifications of the miR9 fa mily // Br. J. Haematol. 2011. Vol. 155 (1). P. 73–83. doi: 10.1111/j.1365-2141.2011.08812.x.</mixed-citation><mixed-citation xml:lang="en">Rodriguez-Otero P., Román-Gómez J., Vilas-Zornoza A. et al. (2011). Deregulation of FGFR1 and CDK6 oncogenic pathways in acute lymphoblastic leukaemia harbouring epigenetic modifications of the miR9 family. Br. J. Haematol., 155 (1), 73–83. doi: 10.1111/j.1365-2141.2011.08812.x.</mixed-citation></citation-alternatives></ref><ref id="cit70"><label>70</label><citation-alternatives><mixed-citation xml:lang="ru">Gao L., Cheng D., Yang J. et al. Sulforaphane epigenetically demethylates the CpG sites of the miR- 9-3 promoter and reactivates miR-9-3 expression in human lung cancer A549 cells // J. Nutr. Biochem. 2018. Vol. 56. P. 109–115. doi: 10.1016/j.jnutbio.2018.01.015.</mixed-citation><mixed-citation xml:lang="en">Gao L., Cheng D., Yang J. et al. (2018). Sulforaphane epigenetically demethylates the CpG sites of the miR- 9-3 promoter and reactivates miR-9-3 expression in human lung cancer A549 cells. J. Nutr. Biochem., 56, 109–115. doi: 10.1016/j.jnutbio.2018.01.015.</mixed-citation></citation-alternatives></ref><ref id="cit71"><label>71</label><citation-alternatives><mixed-citation xml:lang="ru">Emmrich S., Katsman-Kuipers J.E., Henke K. et al. miR-9 is a tumor suppressor in pediatric AML with t(8;21) // Leukemia. 2014. Vol. 28 (5). P. 1022–1032. doi: 10.1038/leu.2013.357.</mixed-citation><mixed-citation xml:lang="en">Emmrich S., Katsman-Kuipers J.E., Henke K. et al. (2014). miR-9 is a tumor suppressor in pediatric AML with t(8;21). Leukemia, 28 (5), 1022–1032. doi: 10.1038/leu.2013.357.</mixed-citation></citation-alternatives></ref><ref id="cit72"><label>72</label><citation-alternatives><mixed-citation xml:lang="ru">Kim B.G., Gao M.Q., Kang S. et al. Mechanical compression induces VEGFA overexpression in breast cancer via DNMT3A-dependent miR-9 downregulation // Cell Death Dis. 2017. Vol. 8 (3): e2646. doi: 10.1038/cddis.2017.73.</mixed-citation><mixed-citation xml:lang="en">Kim B.G., Gao M.Q., Kang S. et al. (2017). Mechanical compression induces VEGFA overexpression in breast cancer via DNMT3A-dependent miR-9 downregulation. Cell Death Dis., 8 (3), e2646. doi: 10.1038/cddis.2017.73.</mixed-citation></citation-alternatives></ref><ref id="cit73"><label>73</label><citation-alternatives><mixed-citation xml:lang="ru">Liu S., Kumar S.M., Lu H. et al. MicroRNA-9 up-regulates E-cadherin through inhibition of NF-κB1-Snail1 pathway in melanoma // J. Pathol. 2012. Vol. 226 (1). P. 61–72. doi: 10.1002/path.2964.</mixed-citation><mixed-citation xml:lang="en">Liu S., Kumar S.M., Lu H. et al. (2012). MicroRNA-9 up-regulates E-cadherin through inhibition of NF-κB1-Snail1 pathway in melanoma. J. Pathol., 226 (1), 61–72. doi: 10.1002/path.2964.</mixed-citation></citation-alternatives></ref><ref id="cit74"><label>74</label><citation-alternatives><mixed-citation xml:lang="ru">Senyuk V., Zhang Y., Liu Y. et al. Critical role of miR-9 in myelopoiesis and EVI1-induced leukemogenesis // Proc. Natl. Acad. Sci. USA. 2013. Vol. 110 (14). P. 5594–5599. doi: 10.1073/pnas.1302645110.</mixed-citation><mixed-citation xml:lang="en">Senyuk V., Zhang Y., Liu Y. et al. (2013). Critical role of miR-9 in myelopoiesis and EVI1-induced leukemogenesis. Proc. Natl. Acad. Sci. USA, 110 (14), 5594– 5599. doi: 10.1073/pnas.1302645110.</mixed-citation></citation-alternatives></ref><ref id="cit75"><label>75</label><citation-alternatives><mixed-citation xml:lang="ru">Panuzzo C., Signorino E., Calabrese C. et al. Landscape of tumor suppressor mutations in acute myeloid leukemia // J. Clin. Med. 2020. Vol. 9 (3): 802. doi: 10.3390/jcm9030802.</mixed-citation><mixed-citation xml:lang="en">Panuzzo C., Signorino E., Calabrese C. et al. (2020). Landscape of tumor suppressor mutations in acute myeloid leukemia. J. Clin. Med., 9 (3), 802. doi: 10.3390/jcm9030802.</mixed-citation></citation-alternatives></ref><ref id="cit76"><label>76</label><citation-alternatives><mixed-citation xml:lang="ru">Zhou L., Fu L., Lv N. et al. A minicircuitry comprised of microRNA-9 and SIRT1 contributes to leukemogenesis in t(8;21) acute myeloid leukemia // Eur. Rev. Med. Pharmacol. Sci. 2017. Vol. 21 (4). P. 786–794.</mixed-citation><mixed-citation xml:lang="en">Zhou L., Fu L., Lv N. et al. (2017). A minicircuitry comprised of microRNA-9 and SIRT1 contributes to leukemogenesis in t(8;21) acute myeloid leukemia. Eur. Rev. Med. Pharmacol. Sci., 21 (4), 786–794.</mixed-citation></citation-alternatives></ref><ref id="cit77"><label>77</label><citation-alternatives><mixed-citation xml:lang="ru">Alhasan L. MiR-126 modulates angiogenesis in breast cancer by targeting VEGF-A-mRNA // Asian Pac. J. Cancer Prev. 2019. Vol. 20 (1). P. 193–197. doi: 10.31557/APJCP.2019.20.1.193.</mixed-citation><mixed-citation xml:lang="en">Alhasan L. (2019). MiR-126 modulates angiogenesis in breast cancer by targeting VEGF-A-mRNA. Asian Pac. J. Cancer Prev., 20 (1), 193–197. doi: 10.31557/APJCP.2019.20.1.193.</mixed-citation></citation-alternatives></ref><ref id="cit78"><label>78</label><citation-alternatives><mixed-citation xml:lang="ru">Saito Y., Friedman G.F., Chihara Y. et al. Epigenetic therapy upregulates the tumour suppressor microRNA-126 and its host gene EGFL7 in human cancer cells // Biochem. Biophys. Res. Commun. 2009. Vol. 379 (3). P. 726–731. doi: 10.1016/j.bbrc.2008.12.098.</mixed-citation><mixed-citation xml:lang="en">Saito Y., Friedman G.F., Chihara Y. et al. (2009). Epigenetic therapy upregulates the tumour suppressor microRNA-126 and its host gene EGFL7 in human cancer cells. Biochem. Biophys. Res. Commun., 379 (3), 726–731. doi: 10.1016/j.bbrc.2008.12.098.</mixed-citation></citation-alternatives></ref><ref id="cit79"><label>79</label><citation-alternatives><mixed-citation xml:lang="ru">Zhao C., Li Y., Zhang M., Yang Y., Chang L. miR-126 inhibits cell proliferation and induces cell apoptosis of hepatocellular carcinoma cells partially by targeting Sox2 // Hum. Cell. 2015. Vol. 28 (2). P. 91–99. doi: 10.1007/s13577-014-0105-z.</mixed-citation><mixed-citation xml:lang="en">Zhao C., Li Y., Zhang M., Yang Y., Chang L. (2015). miR-126 inhibits cell proliferation and induces cell apoptosis of hepatocellular carcinoma cells partially by targeting Sox2. Hum. Cell, 28 (2), 91–99. doi: 10.1007/s13577-014-0105-z.</mixed-citation></citation-alternatives></ref><ref id="cit80"><label>80</label><citation-alternatives><mixed-citation xml:lang="ru">Li F. Expression and correlation of miR-124 and miR- 126 in breast cancer // Oncol. Lett. 2019. Vol. 17 (6). P. 5115–5119. doi: 10.3892/ol.2019.10184.</mixed-citation><mixed-citation xml:lang="en">Li F. (2019). Expression and correlation of miR-124 and miR-126 in breast cancer. Oncol. Lett., 17 (6), 5115–5119. doi: 10.3892/ol.2019.10184.</mixed-citation></citation-alternatives></ref><ref id="cit81"><label>81</label><citation-alternatives><mixed-citation xml:lang="ru">Liu R., Zhang Y.S., Zhang S. et al. MiR-126-3p suppresses the growth, migration and invasion of NSCLC via targeting CCR1 // Eur. Rev. Med. Pharmacol. Sci. 2019. Vol. 23 (2). P. 679–689. doi: 10.26355/eurrev_201901_16881.</mixed-citation><mixed-citation xml:lang="en">Liu R., Zhang Y.S., Zhang S. et al. (2019). MiR-126-3p suppresses the growth, migration and invasion of NSCLC via targeting CCR1. Eur. Rev. Med. Pharmacol. Sci., 23 (2), 679–689. doi: 10.26355/eurrev_201901_16881.</mixed-citation></citation-alternatives></ref><ref id="cit82"><label>82</label><citation-alternatives><mixed-citation xml:lang="ru">Moradi Sarabi M., Zahedi S.A., Pajouhi N. et al. The effects of dietary polyunsaturated fatty acids on miR- 126 promoter DNA methylation status and VEGF protein expression in the colorectal cancer cells // Genes Nutr. 2018. Vol. 13: 32. doi: 10.1186/s12263-018-0623-5.</mixed-citation><mixed-citation xml:lang="en">Moradi Sarabi M., Zahedi S.A., Pajouhi N. et al. (2018). The effects of dietary polyunsaturated fatty acids on miR-126 promoter DNA methylation status and VEGF protein expression in the colorectal cancer cells. Genes Nutr., 13, 32. doi: 10.1186/s12263-018-0623-5.</mixed-citation></citation-alternatives></ref><ref id="cit83"><label>83</label><citation-alternatives><mixed-citation xml:lang="ru">Miao Y., Lu J., Fan B., Sun L. MicroRNA-126-5p inhibits the migration of breast cancer cells by directly targeting CNOT7 // Technol. Cancer Res. Treat. 2020. Vol. 19: 1533033820977545. doi: 10.1177/1533033820977545.</mixed-citation><mixed-citation xml:lang="en">Miao Y., Lu J., Fan B., Sun L. (2020). MicroRNA- 126-5p inhibits the migration of breast cancer cells by directly targeting CNOT7. Technol. Cancer Res. Treat., 19, 1533033820977545. doi: 10.1177/1533033820977545.</mixed-citation></citation-alternatives></ref><ref id="cit84"><label>84</label><citation-alternatives><mixed-citation xml:lang="ru">Yu J., Fan Q., Li L. The MCM3AP-AS1/miR-126/ VEGF axis regulates cancer cell invasion and migration in endometrioid carcinoma // World J. Surg. Oncol. 2021. Vol. 19 (1): 213. doi: 10.1186/s12957-021-02316-0.</mixed-citation><mixed-citation xml:lang="en">Yu J., Fan Q., Li L. (2021). The MCM3AP-AS1/miR- 126/VEGF axis regulates cancer cell invasion and migration in endometrioid carcinoma. World J. Surg. Oncol., 19 (1), 213. doi: 10.1186/s12957-021-02316-0.</mixed-citation></citation-alternatives></ref><ref id="cit85"><label>85</label><citation-alternatives><mixed-citation xml:lang="ru">Chen S.R., Cai W.P., Dai X.J. et al. Research on miR- 126 in glioma targeted regulation of PTEN/PI3K/ Akt and MDM2-p53 pathways // Eur. Rev. Med. Pharmacol. Sci. 2019. Vol. 23 (8). P. 3461–3470. doi: 10.26355/eurrev_201904_17711.</mixed-citation><mixed-citation xml:lang="en">Chen S.R., Cai W.P., Dai X.J. et al. (2019). Research on miR-126 in glioma targeted regulation of PTEN/ PI3K/Akt and MDM2-p53 pathways. Eur. Rev. Med. Pharmacol. Sci., 23 (8), 3461–3470. doi: 10.26355/eurrev_201904_17711.</mixed-citation></citation-alternatives></ref><ref id="cit86"><label>86</label><citation-alternatives><mixed-citation xml:lang="ru">Chen W., Yu J., Xie R. et al. Roles of the SNHG7/ microRNA-9-5p/DPP4 ceRNA network in the growth and 131I resistance of thyroid carcinoma cells through PI3K/Akt activation // Oncol. Rep. 2021. Vol. 45 (4): 3. doi: 10.3892/or.2021.7954.</mixed-citation><mixed-citation xml:lang="en">Chen W., Yu J., Xie R. et al. (2021). Roles of the SNHG7/microRNA-9-5p/DPP4 ceRNA network in the growth and 131I resistance of thyroid carcinoma cells through PI3K/Akt activation. Oncol. Rep., 45 (4), 3. doi: 10.3892/or.2021.7954.</mixed-citation></citation-alternatives></ref><ref id="cit87"><label>87</label><citation-alternatives><mixed-citation xml:lang="ru">Takashima Y., Kawaguchi A., Iwadate Y. et al. MicroRNA signature constituted of miR-30d, miR- 93, and miR-181b is a promising prognostic marker in primary central nervous system lymphoma // PLoS One. 2019. Vol. 14 (1): e0210400. doi: 10.1371/journal.pone.0210400.</mixed-citation><mixed-citation xml:lang="en">Takashima Y., Kawaguchi A., Iwadate Y. et al. (2019). MicroRNA signature constituted of miR-30d, miR- 93, and miR-181b is a promising prognostic marker in primary central nervous system lymphoma. PLoS One, 14 (1), e0210400. doi: 10.1371/journal.pone.0210400.</mixed-citation></citation-alternatives></ref><ref id="cit88"><label>88</label><citation-alternatives><mixed-citation xml:lang="ru">Chen H.H., Huang W.T., Yang L.W., Lin C.W. The PTEN-AKT-mTOR/RICTOR pathway in nasal natural killer cell lymphoma is activated by miR-494-3p via PTEN but inhibited by miR-142-3p via RICTOR // Am. J. Pathol. 2015. Vol. 185 (5). P. 1487–1499. doi: 10.1016/j.ajpath.2015.01.025.</mixed-citation><mixed-citation xml:lang="en">Chen H.H., Huang W.T., Yang L.W., Lin C.W. (2015). The PTEN-AKT-mTOR/RICTOR pathway in nasal natural killer cell lymphoma is activated by miR- 494-3p via PTEN but inhibited by miR-142-3p via RICTOR. Am. J. Pathol., 185 (5), 1487–1499. doi: 10.1016/j.ajpath.2015.01.025.</mixed-citation></citation-alternatives></ref><ref id="cit89"><label>89</label><citation-alternatives><mixed-citation xml:lang="ru">Bong I.P.N., Ng C.C., Baharuddin P., Zakaria Z. MicroRNA expression patterns and target prediction in multiple myeloma development and malignancy // Genes Genomics. 2017. Vol. 39 (5). P. 533–540. doi: 10.1007/s13258-017-0518-7.</mixed-citation><mixed-citation xml:lang="en">Bong I.P.N., Ng C.C., Baharuddin P., Zakaria Z. (2017). MicroRNA expression patterns and target prediction in multiple myeloma development and malignancy. Genes Genomics, 39 (5), 533–540. doi: 10.1007/s13258-017-0518-7.</mixed-citation></citation-alternatives></ref><ref id="cit90"><label>90</label><citation-alternatives><mixed-citation xml:lang="ru">Andrade T.A., Evangelista A.F., Campos A.H. et al. A microRNA signature profile in EBV+ diffuse large B-cell lymphoma of the elderly // Oncotarget. 2014. Vol. 5 (23). P. 11813–11826. doi: 10.18632/oncotarget.</mixed-citation><mixed-citation xml:lang="en">Andrade T.A., Evangelista A.F., Campos A.H. et al. (2014). A microRNA signature profile in EBV+ diffuse large B-cell lymphoma of the elderly. Oncotarget, 5 (23), 11813–11826. doi: 10.18632/oncotarget.</mixed-citation></citation-alternatives></ref><ref id="cit91"><label>91</label><citation-alternatives><mixed-citation xml:lang="ru">Borges N.M., do Vale Elias M., Fook-Alves V.L. et al. AngiomiRs expression profiling in diffuse large B-Cell lymphoma // Oncotarget. 2016. Vol. 7 (4). P. 4806– 4816. doi: 10.18632/oncotarget.6624.</mixed-citation><mixed-citation xml:lang="en">Borges N.M., do Vale Elias M., Fook-Alves V.L. et al. (2016). AngiomiRs expression profiling in diffuse large B-Cell lymphoma. Oncotarget, 7 (4), 4806– 4816. doi: 10.18632/oncotarget.6624.</mixed-citation></citation-alternatives></ref><ref id="cit92"><label>92</label><citation-alternatives><mixed-citation xml:lang="ru">Li Z., Lu J., Sun M. et al. Distinct microRNA expression profiles in acute myeloid leukemia with common translocations // Sci. USA. 2008. Vol. 105 (40). P. 15535–15540. doi: 10.1073/pnas.0808266105.</mixed-citation><mixed-citation xml:lang="en">Li Z., Lu J., Sun M. et al. (2008). Distinct microRNA expression profiles in acute myeloid leukemia with common translocations. Sci. USA, 105 (40), 15535– 15540. doi: 10.1073/pnas.0808266105.</mixed-citation></citation-alternatives></ref><ref id="cit93"><label>93</label><citation-alternatives><mixed-citation xml:lang="ru">Cammarata G., Augugliaro L., Salemi D. et al. Differential expression of specific microRNA and their targets in acute myeloid leukemia // Am. J. Hematol. 2010. Vol. 85 (5). P. 331–339. doi: 10.1002/ajh.21667.</mixed-citation><mixed-citation xml:lang="en">Cammarata G., Augugliaro L., Salemi D. et al. (2010). Differential expression of specific microRNA and their targets in acute myeloid leukemia. Am. J. Hematol., 85 (5), 331–339. doi: 10.1002/ajh.21667.</mixed-citation></citation-alternatives></ref><ref id="cit94"><label>94</label><citation-alternatives><mixed-citation xml:lang="ru">Peveling-Oberhag J., Crisman G., Schmidt A. et al. Dysregulation of global microRNA expression in splenic marginal zone lymphoma and influence of chronic hepatitis C virus infection // Leukemia. 2012. Vol. 26 (7). P. 1654–1662. doi: 10.1038/leu.2012.29.</mixed-citation><mixed-citation xml:lang="en">Peveling-Oberhag J., Crisman G., Schmidt A. et al. (2012). Dysregulation of global microRNA expression in splenic marginal zone lymphoma and influence of chronic hepatitis C virus infection. Leukemia, 26 (7), 1654–1662. doi: 10.1038/leu.2012.29.</mixed-citation></citation-alternatives></ref><ref id="cit95"><label>95</label><citation-alternatives><mixed-citation xml:lang="ru">Schoof E.M., Lechman E.R., Dick J.E. Global proteomics dataset of miR-126 overexpression in acute myeloid leukemia // Data Brief. 2016. Vol. 9. P. 57–61. doi: 10.1016/j.dib.2016.07.035.</mixed-citation><mixed-citation xml:lang="en">Schoof E.M., Lechman E.R., Dick J.E. (2016). Global proteomics dataset of miR-126 overexpression in acute myeloid leukemia. Data Brief, 9, 57–61. doi: 10.1016/j.dib.2016.07.035.</mixed-citation></citation-alternatives></ref><ref id="cit96"><label>96</label><citation-alternatives><mixed-citation xml:lang="ru">Ishihara K., Sasaki D., Tsuruda K. et al. Impact of miR- 155 and miR-126 as novel biomarkers on the assessment of disease progression and prognosis in adult T-cell leukemia // Cancer Epidemiol. 2012. Vol. 36 (6). P. 560–565. doi: 10.1016/j.canep.2012.07.002.</mixed-citation><mixed-citation xml:lang="en">Ishihara K., Sasaki D., Tsuruda K. et al. (2012). Impact of miR-155 and miR-126 as novel biomarkers on the assessment of disease progression and prognosis in adult T-cell leukemia. Cancer Epidemiol., 36 (6), 560–565. doi: 10.1016/j.canep.2012.07.002.</mixed-citation></citation-alternatives></ref><ref id="cit97"><label>97</label><citation-alternatives><mixed-citation xml:lang="ru">Kopp K.L., Ralfkiaer U., Nielsen B.S. et al. Expression of miR-155 and miR-126 in situ in cutaneous T-cell lymphoma // APMIS. 2013. Vol. 121 (11). P. 1020– 1024. doi: 10.1111/apm.12162.</mixed-citation><mixed-citation xml:lang="en">Kopp K.L., Ralfkiaer U., Nielsen B.S. et al. (2013). Expression of miR-155 and miR-126 in situ in cutaneous T-cell lymphoma. APMIS, 121 (11), 1020–1024. doi: 10.1111/apm.12162.</mixed-citation></citation-alternatives></ref><ref id="cit98"><label>98</label><citation-alternatives><mixed-citation xml:lang="ru">Cao D., Zhao M., Wan C. et al. Role of tea polyphenols in delaying hyperglycemia-induced senescence in human glomerular mesangial cells via miR-126/Aktp53-p21 pathways // Int. Urol. Nephrol. 2019. Vol. 51 (6). P. 1071–1078. doi: 10.1007/s11255-019-02165-7.</mixed-citation><mixed-citation xml:lang="en">Cao D., Zhao M., Wan C. et al. (2019). Role of tea polyphenols in delaying hyperglycemia-induced senescence in human glomerular mesangial cells via miR- 126/Akt-p53-p21 pathways. Int. Urol. Nephrol., 51 (6), 1071–1078. doi: 10.1007/s11255-019-02165-7.</mixed-citation></citation-alternatives></ref><ref id="cit99"><label>99</label><citation-alternatives><mixed-citation xml:lang="ru">Cao D.W., Jiang C.M., Wan C. et al. Upregulation of miR-126 delays the senescence of human glomerular mesangial cells induced by high glucose via telomerep53-p21-Rb signaling pathway // Curr. Med. Sci. 2018. Vol. 38 (5). P. 758–764. doi: 10.1007/s11596-018-1942-x.</mixed-citation><mixed-citation xml:lang="en">Cao D.W., Jiang C.M., Wan C. et al. (2018). Upregulation of miR-126 delays the senescence of human glomerular mesangial cells induced by high glucose via telomere-p53-p21-Rb signaling pathway. Curr. Med. Sci., 38 (5), 758–764. doi: 10.1007/s11596-018-1942-x.</mixed-citation></citation-alternatives></ref><ref id="cit100"><label>100</label><citation-alternatives><mixed-citation xml:lang="ru">Heissig B., Salama Y., Takahashi S., Okumura K., Hattori K. The multifaceted roles of EGFL7 in cancer and drug resistance // Cancers (Basel). 2021. Vol. 13 (5): 1014. doi: 10.3390/cancers13051014.</mixed-citation><mixed-citation xml:lang="en">Heissig B., Salama Y., Takahashi S., Okumura K., Hattori K. (2021). The multifaceted roles of EGFL7 in cancer and drug resistance. Cancers (Basel), 13 (5), 1014. doi: 10.3390/cancers13051014.</mixed-citation></citation-alternatives></ref><ref id="cit101"><label>101</label><citation-alternatives><mixed-citation xml:lang="ru">Tomasetti M., Gaetani S., Monaco F., Neuzil J., Santarelli L. Epigenetic regulation of miRNA expression in malignant mesothelioma: miRNAs as biomarkers of early diagnosis and therapy // Front. Oncol. 2019. Vol. 9: 1293. doi: 10.3389/fonc.2019.01293.</mixed-citation><mixed-citation xml:lang="en">Tomasetti M., Gaetani S., Monaco F., Neuzil J., Santarelli L. (2019). Epigenetic regulation of miRNA expression in malignant mesothelioma: miRNAs as biomarkers of early diagnosis and therapy. Front. Oncol., 9, 1293. doi: 10.3389/fonc.2019.01293.</mixed-citation></citation-alternatives></ref><ref id="cit102"><label>102</label><citation-alternatives><mixed-citation xml:lang="ru">Wu C.L., Shan T.D., Han Y. et al. Long intergenic noncoding RNA 00665 promotes proliferation and inhibits apoptosis in colorectal cancer by regulating miR-126-5p // Aging (Albany NY). 2021. Vol. 13 (10). P. 13571–13584. doi: 10.18632/aging.202874.</mixed-citation><mixed-citation xml:lang="en">Wu C.L., Shan T.D., Han Y. et al. (2021). Long intergenic noncoding RNA 00665 promotes proliferation and inhibits apoptosis in colorectal cancer by regulating miR-126-5p. Aging (Albany NY), 13 (10), 13571– 13584. doi: 10.18632/aging.202874.</mixed-citation></citation-alternatives></ref><ref id="cit103"><label>103</label><citation-alternatives><mixed-citation xml:lang="ru">Chen Q., Chen S., Zhao J., Zhou Y., Xu L. MicroRNA-126: A new and promising player in lung cancer // Oncol. Lett. 2021. Vol. 21 (1): 35. doi: 10.3892/ol.2020.12296.</mixed-citation><mixed-citation xml:lang="en">Chen Q., Chen S., Zhao J., Zhou Y., Xu L. (2021). MicroRNA-126: A new and promising player in lung cancer. Oncol. Lett., 21 (1), 35. doi: 10.3892/ol.2020.12296.</mixed-citation></citation-alternatives></ref><ref id="cit104"><label>104</label><citation-alternatives><mixed-citation xml:lang="ru">Li M., Meng X., Li M. MiR-126 promotes esophageal squamous cell carcinoma via inhibition of apoptosis and autophagy // Aging (Albany NY). 2020. Vol. 12 (12). P. 12107–12118. doi: 10.18632/aging.103379.</mixed-citation><mixed-citation xml:lang="en">Li M., Meng X., Li M. (2020). MiR-126 promotes esophageal squamous cell carcinoma via inhibition of apoptosis and autophagy. Aging (Albany NY), 12 (12), 12107–12118. doi: 10.18632/aging.103379.</mixed-citation></citation-alternatives></ref><ref id="cit105"><label>105</label><citation-alternatives><mixed-citation xml:lang="ru">Cui H., Mu Y., Yu L. et al. Methylation of the miR- 126 gene associated with glioma progression // Fam. Cancer. 2016. Vol. 15 (2). P. 317–324. doi: 10.1007/s10689-015-9846-4.</mixed-citation><mixed-citation xml:lang="en">Cui H., Mu Y., Yu L. et al. (2016). Methylation of the miR-126 gene associated with glioma progression. Fam. Cancer, 15 (2), 317–324. doi: 10.1007/s10689-015-9846-4.</mixed-citation></citation-alternatives></ref><ref id="cit106"><label>106</label><citation-alternatives><mixed-citation xml:lang="ru">Li W., Kong X., Huang T. et al. Bioinformatic analysis and in vitro validation of a five-microRNA signature as a prognostic biomarker of hepatocellular carcinoma // Ann. Transl. Med. 2020. Vol. 8 (21): 1422. doi: 10.21037/atm-20-2509.</mixed-citation><mixed-citation xml:lang="en">Li W., Kong X., Huang T. et al. (2020). Bioinformatic analysis and in vitro validation of a five-microRNA signature as a prognostic biomarker of hepatocellular carcinoma. Ann. Transl. Med., 8 (21), 1422. doi: 10.21037/atm-20-2509.</mixed-citation></citation-alternatives></ref><ref id="cit107"><label>107</label><citation-alternatives><mixed-citation xml:lang="ru">Duan J., Lu G., Li Y. et al. miR-137 functions as a tumor suppressor gene in pituitary adenoma by targeting AKT2 // Int. J. Clin. Exp. Pathol. 2019. Vol. 12 (5). P. 1557–1564.</mixed-citation><mixed-citation xml:lang="en">Duan J., Lu G., Li Y. et al. (2019). miR-137 functions as a tumor suppressor gene in pituitary adenoma by targeting AKT2. Int. J. Clin. Exp. Pathol., 12 (5), 1557– 1564.</mixed-citation></citation-alternatives></ref><ref id="cit108"><label>108</label><citation-alternatives><mixed-citation xml:lang="ru">Zang Y., Zhu J., Li Q. et al. miR-137-3p modulates the progression of prostate cancer by regulating the JNK3/EZH2 axis // Onco Targets Ther. 2020. Vol. 13. P. 7921–7932. doi: 10.2147/OTT.S256161.</mixed-citation><mixed-citation xml:lang="en">Zang Y., Zhu J., Li Q. et al. (2020). miR-137-3p modulates the progression of prostate cancer by regulating the JNK3/EZH2 axis. Onco Targets Ther., 13, 7921– 7932. doi: 10.2147/OTT.S256161.</mixed-citation></citation-alternatives></ref><ref id="cit109"><label>109</label><citation-alternatives><mixed-citation xml:lang="ru">Ding F., Zhang S., Gao S. et al. MiR-137 functions as a tumor suppressor in pancreatic cancer by targeting MRGBP // J. Cell Biochem. 2018. Vol. 119 (6). P. 4799–4807. doi: 10.1002/jcb.26676.</mixed-citation><mixed-citation xml:lang="en">Ding F., Zhang S., Gao S. et al. (2018). MiR-137 functions as a tumor suppressor in pancreatic cancer by targeting MRGBP. J. Cell Biochem., 119 (6), 4799– 4807. doi: 10.1002/jcb.26676.</mixed-citation></citation-alternatives></ref><ref id="cit110"><label>110</label><citation-alternatives><mixed-citation xml:lang="ru">Wang M., Gao H., Qu H. et al. MiR-137 suppresses tumor growth and metastasis in clear cell renal cell carcinoma // Pharmacol. Reports. 2018. Vol. 70 (5). P. 963–971. doi: 10.1016/j.pharep.2018.04.006.</mixed-citation><mixed-citation xml:lang="en">Wang M., Gao H., Qu H. et al. (2018). MiR-137 suppresses tumor growth and metastasis in clear cell renal cell carcinoma. Pharmacol. Reports, 70 (5), 963–971. doi: 10.1016/j.pharep.2018.04.006.</mixed-citation></citation-alternatives></ref><ref id="cit111"><label>111</label><citation-alternatives><mixed-citation xml:lang="ru">Zhang W., Chen J.H., Shan T. et al. miR-137 is a tumor suppressor in endometrial cancer and is repressed by DNA hypermethylation // Lab. Invest. 2018. Vol. 98 (11). P. 1397–1407. doi: 10.1038/s41374-018-0092-x.</mixed-citation><mixed-citation xml:lang="en">Zhang W., Chen J.H., Shan T. et al. (2018). miR-137 is a tumor suppressor in endometrial cancer and is repressed by DNA hypermethylation. Lab. Invest., 98 (11), 1397–1407. doi: 10.1038/s41374-018-0092-x.</mixed-citation></citation-alternatives></ref><ref id="cit112"><label>112</label><citation-alternatives><mixed-citation xml:lang="ru">Huang B., Huang M., Li Q. miR-137 suppresses migration and invasion by targeting EZH2-STAT3 signaling in human hepatocellular carcinoma // Pathol. Res. Pract. 2018. Vol. 214 (12). P. 1980–1986. doi: 10.1016/j.prp.2018.08.005.</mixed-citation><mixed-citation xml:lang="en">Huang B., Huang M., Li Q. (2018). miR-137 suppresses migration and invasion by targeting EZH2- STAT3 signaling in human hepatocellular carcinoma. Pathol. Res. Pract., 214 (12), 1980–1986. doi: 10.1016/j.prp.2018.08.005.</mixed-citation></citation-alternatives></ref><ref id="cit113"><label>113</label><citation-alternatives><mixed-citation xml:lang="ru">Bi W.P., Xia M., Wang X.J. miR-137 suppresses proliferation, migration and invasion of colon cancer cell lines by targeting TCF4 // Oncol. Lett. 2018. Vol. 15 (6). P. 8744–8748. doi: 10.3892/ol.2018.8364.</mixed-citation><mixed-citation xml:lang="en">Bi W.P., Xia M., Wang X.J. (2018). miR-137 suppresses proliferation, migration and invasion of colon cancer cell lines by targeting TCF4. Oncol. Lett., 15 (6), 8744–8748. doi: 10.3892/ol.2018.8364.</mixed-citation></citation-alternatives></ref><ref id="cit114"><label>114</label><citation-alternatives><mixed-citation xml:lang="ru">Liu X., Chen L., Tian X.D., Zhang T. MiR-137 and its target TGFA modulate cell growth and tumorigenesis of non-small cell lung cancer // Eur. Rev. Med. Pharmacol. Sci. 2017. Vol. 21 (3). P. 511–517.</mixed-citation><mixed-citation xml:lang="en">Liu X., Chen L., Tian X.D., Zhang T. (2017). MiR-137 and its target TGFA modulate cell growth and tumorigenesis of non-small cell lung cancer. Eur. Rev. Med. Pharmacol. Sci., 21 (3), 511–517.</mixed-citation></citation-alternatives></ref><ref id="cit115"><label>115</label><citation-alternatives><mixed-citation xml:lang="ru">Wang Y., Chen R., Zhou X. et al. miR-137: a novel therapeutic target for human glioma // Mol. Ther. Nucleic Acids. 2020. Vol. 21. P. 614–622. doi: 10.1016/j.omtn.2020.06.028.</mixed-citation><mixed-citation xml:lang="en">Wang Y., Chen R., Zhou X. et al. (2020). miR-137: a novel therapeutic target for human glioma. Mol. Ther. Nucleic Acids, 21, 614–622. doi: 10.1016/j.omtn.2020.06.028.</mixed-citation></citation-alternatives></ref><ref id="cit116"><label>116</label><citation-alternatives><mixed-citation xml:lang="ru">Huang Y., Zou Y., Zheng R., Ma X. MiR-137 inhibits cell proliferation in acute lymphoblastic leukemia by targeting JARID1B // Eur. J. Haematol. 2019. Vol. 103 (3). P. 215–224. doi: 10.1111/ejh.13276.</mixed-citation><mixed-citation xml:lang="en">Huang Y., Zou Y., Zheng R., Ma X. (2019). MiR-137 inhibits cell proliferation in acute lymphoblastic leukemia by targeting JARID1B. Eur. J. Haematol., 103 (3), 215–224. doi: 10.1111/ejh.13276.</mixed-citation></citation-alternatives></ref><ref id="cit117"><label>117</label><citation-alternatives><mixed-citation xml:lang="ru">Abdi J., Jian H., Chang H. Role of micro-RNAs in drug resistance of multiple myeloma // Oncotarget. 2016. Vol. 7 (37). P. 60723–60735. doi: 10.18632/oncotarget.11032.</mixed-citation><mixed-citation xml:lang="en">Abdi J., Jian H., Chang H. (2016). Role of micro-RNAs in drug resistance of multiple myeloma. Oncotarget, 7 (37), 60723–60735. doi: 10.18632/oncotarget.11032.</mixed-citation></citation-alternatives></ref><ref id="cit118"><label>118</label><citation-alternatives><mixed-citation xml:lang="ru">Qin Y., Zhang S., Deng S. et al. Epigenetic silencing of miR-137 induces drug resistance and chromosomal instability by targeting AURKA in multiple myeloma // Leukemia. 2017. Vol. 31 (5). P. 1123–1135. doi: 10.1038/leu.2016.325.</mixed-citation><mixed-citation xml:lang="en">Qin Y., Zhang S., Deng S. et al. (2017). Epigenetic silencing of miR-137 induces drug resistance and chromosomal instability by targeting AURKA in multiple myeloma. Leukemia, 31 (5), 1123–1135. doi: 10.1038/leu.2016.325.</mixed-citation></citation-alternatives></ref><ref id="cit119"><label>119</label><citation-alternatives><mixed-citation xml:lang="ru">Yang Y., Li F., Saha M.N. et al. miR-137 and miR-197 induce apoptosis and suppress tumorigenicity by targeting MCL-1 in multiple myeloma // Clin. Cancer Res. 2015. Vol. 21 (10). P. 2399–2411. doi: 10.1158/1078-0432.CCR-14-1437.</mixed-citation><mixed-citation xml:lang="en">Yang Y., Li F., Saha M.N. et al. (2015). miR-137 and miR-197 induce apoptosis and suppress tumorigenicity by targeting MCL-1 in multiple myeloma. Clin. Cancer Res., 21 (10), 2399–2411. doi: 10.1158/1078-0432.CCR-14-1437.</mixed-citation></citation-alternatives></ref><ref id="cit120"><label>120</label><citation-alternatives><mixed-citation xml:lang="ru">Kozaki K., Imoto I., Mogi S., Omura K., Inazawa J. Exploration of tumor-suppressive microRNAs silenced by DNA hypermethylation in oral cancer // Cancer Res. 2008. Vol. 68 (7). P. 2094–2105. doi: 10.1158/0008-5472.CAN-07-5194.</mixed-citation><mixed-citation xml:lang="en">Kozaki K., Imoto I., Mogi S., Omura K., Inazawa J. (2008). Exploration of tumor-suppressive micro RNAs silenced by DNA hypermethylation in oral cancer. Cancer Res., 68 (7), 2094–2105. doi: 10.1158/0008-5472.CAN-07-5194.</mixed-citation></citation-alternatives></ref><ref id="cit121"><label>121</label><citation-alternatives><mixed-citation xml:lang="ru">Chen X., Wang J., Shen H. et al. Epigenetics, microRNAs, and carcinogenesis: functional role of microRNA-137 in uveal melanoma // Invest. Ophthalmol. Vis. Sci. 2011. Vol. 52 (3). P. 1193–1199. doi: 10.1167/iovs.10-5272.</mixed-citation><mixed-citation xml:lang="en">Chen X., Wang J., Shen H. et al. (2011). Epigenetics, microRNAs, and carcinogenesis: functional role of microRNA-137 in uveal melanoma. Invest. Ophthalmol. Vis. Sci., 52 (3), 1193–1199. doi: 10.1167/iovs.10-5272.</mixed-citation></citation-alternatives></ref><ref id="cit122"><label>122</label><citation-alternatives><mixed-citation xml:lang="ru">Zhu X., Li Y., Shen H. et al. miR-137 inhibits the proliferation of lung cancer cells by targeting Cdc42 and Cdk6 // FEBS Lett. 2013. Vol. 587 (1). P. 73–81. doi: 10.1016/j.febslet.2012.11.004.</mixed-citation><mixed-citation xml:lang="en">Zhu X., Li Y., Shen H. et al. (2013). miR-137 inhibits the proliferation of lung cancer cells by targeting Cdc42 and Cdk6. FEBS Lett., 587 (1), 73–81. doi: 10.1016/j.febslet.2012.11.004.</mixed-citation></citation-alternatives></ref><ref id="cit123"><label>123</label><citation-alternatives><mixed-citation xml:lang="ru">Balaguer F., Link A., Lozano J.J. et al. Epigenetic silencing of miR-137 is an early event in colorectal carcinogenesis // Cancer Res. 2010. Vol. 70 (16). P. 6609–6618. doi: 10.1158/0008-5472.</mixed-citation><mixed-citation xml:lang="en">Balaguer F., Link A., Lozano J.J. et al. (2010). Epigenetic silencing of miR-137 is an early event in colorectal carcinogenesis. Cancer Res., 70 (16), 6609–6618. doi: 10.1158/0008-5472.</mixed-citation></citation-alternatives></ref><ref id="cit124"><label>124</label><citation-alternatives><mixed-citation xml:lang="ru">Langevin S.M., Stone R.A., Bunker C.H. et al. MicroRNA-137 promoter methylation is associated with poorer overall survival in patients with squamous cell carcinoma of the head and neck // Cancer. 2011. Vol. 117 (7). P. 1454–1462. doi: 10.1002/cncr.25689.</mixed-citation><mixed-citation xml:lang="en">Langevin S.M., Stone R.A., Bunker C.H. et al. (2011). MicroRNA-137 promoter methylation is associated with poorer overall survival in patients with squamous cell carcinoma of the head and neck. Cancer, 117 (7), 1454–1462. doi: 10.1002/cncr.25689.</mixed-citation></citation-alternatives></ref><ref id="cit125"><label>125</label><citation-alternatives><mixed-citation xml:lang="ru">Hannafon B.N., Ding W. Functional role of miRNAs in the progression of breast ductal carcinoma in situ // Am. J. Pathol. 2019. Vol. 189 (5). P. 966–974. doi: 10.1016/j.ajpath.2018.06.025.</mixed-citation><mixed-citation xml:lang="en">Hannafon B.N., Ding W. (2019). Functional role of miRNAs in the progression of breast ductal carcinoma in situ. Am. J. Pathol., 189 (5), 966–974. doi: 10.1016/j.ajpath.2018.06.025.</mixed-citation></citation-alternatives></ref><ref id="cit126"><label>126</label><citation-alternatives><mixed-citation xml:lang="ru">Рыков С.В., Ходырев Д.С., Пронина И.В. и др. Новые гены микроРНК, подверженные метилированию в опухолях легкого // Генетика. 2013. Т. 49, № 7. С. 896–901. doi: 10.7868/s0016675813070114.</mixed-citation><mixed-citation xml:lang="en">Rykov S.V., Khodyrev D.S., Pronina I.V. et al. (2013). Novel miRNA genes methylated in lung tumors. Russian Journal of Genetics, 49 (7), 896–901. doi: 10.7868/s0016675813070114.</mixed-citation></citation-alternatives></ref><ref id="cit127"><label>127</label><citation-alternatives><mixed-citation xml:lang="ru">Bondada M.S., Yao Y., Nair V. Multifunctional miR- 155 pathway in avian oncogenic virus-induced neoplastic diseases // Noncoding RNA. 2019. Vol. 5 (1): 24. doi: 10.3390/ncrna5010024.</mixed-citation><mixed-citation xml:lang="en">Bondada M.S., Yao Y., Nair V. (2019). Multifunctional miR-155 pathway in avian oncogenic virus-induced neoplastic diseases. Noncoding RNA, 5 (1), 24. doi: 10.3390/ncrna5010024.</mixed-citation></citation-alternatives></ref><ref id="cit128"><label>128</label><citation-alternatives><mixed-citation xml:lang="ru">Holubekova V., Mendelova A., Jasek K. et al. Epigenetic regulation by DNA methylation and miRNA molecules in cancer // Future Oncol. 2017. Vol. 13 (25). P. 2217–2222. doi: 10.2217/fon-2017-0363.</mixed-citation><mixed-citation xml:lang="en">Holubekova V., Mendelova A., Jasek K. et al. (2017). Epigenetic regulation by DNA methylation and miRNA molecules in cancer. Future Oncol., 13 (25), 2217–2222. doi: 10.2217/fon-2017-0363.</mixed-citation></citation-alternatives></ref><ref id="cit129"><label>129</label><citation-alternatives><mixed-citation xml:lang="ru">Huang Q., Shen Y.J., Hsueh C.Y. et al. miR-17-5p drives G2/M-phase accumulation by directly targeting CCNG2 and is related to recurrence of head and neck squamous cell carcinoma // BMC Cancer. 2021. Vol. 21 (1): 1074. doi: 10.1186/s12885-021-08812-6.</mixed-citation><mixed-citation xml:lang="en">Huang Q., Shen Y.J., Hsueh C.Y. et al. (2021). miR- 17-5p drives G2/M-phase accumulation by directly targeting CCNG2 and is related to recurrence of head and neck squamous cell carcinoma. BMC Cancer, 21 (1), 1074. doi: 10.1186/s12885-021-08812-6.</mixed-citation></citation-alternatives></ref><ref id="cit130"><label>130</label><citation-alternatives><mixed-citation xml:lang="ru">Larrabeiti-Etxebarria A., Lopez-Santillan M., SantosZorrozua B., Lopez-Lopez E., Garcia-Orad A. Systematic review of the potential of microRNAs in diffuse large B cell lymphoma // Cancers (Basel). 2019. Vol. 11 (2): 144. doi: 10.3390/cancers11020144.</mixed-citation><mixed-citation xml:lang="en">Larrabeiti-Etxebarria A., Lopez-Santillan M., SantosZorrozua B., Lopez-Lopez E., Garcia-Orad A. (2019). Systematic review of the potential of microRNAs in diffuse large B cell lymphoma. Cancers (Basel), 11 (2), 144. doi: 10.3390/cancers11020144.</mixed-citation></citation-alternatives></ref><ref id="cit131"><label>131</label><citation-alternatives><mixed-citation xml:lang="ru">Lawrie C., Soneji S., Marafioti T. et al. MicroRNA expression distinguishes between germinal center B cell-like and activated B cell-like subtypes of diffuse large B cell lymphoma // Int. J. Cancer. 2007. Vol. 121. P. 1156–1161. doi: 10.1002/ijc.22800.</mixed-citation><mixed-citation xml:lang="en">Lawrie C., Soneji S., Marafioti T. et al. (2007). MicroRNA expression distinguishes between germinal center B cell-like and activated B cell-like subtypes of diffuse large B cell lymphoma. Int. J. Cancer, 121, 1156–1161. doi: 10.1002/ijc.22800.</mixed-citation></citation-alternatives></ref><ref id="cit132"><label>132</label><citation-alternatives><mixed-citation xml:lang="ru">Lawrie C.H., Gal S., Dunlop H.M. et al. Detection of elevated levels of tumour-associated microRNAs in serum of patients with diffuse large B-cell lymphoma // Br. J. Haematol. 2008. Vol. 141 (5). P. 672– 675. doi: 10.1111/j.1365-2141.2008.07077.x.</mixed-citation><mixed-citation xml:lang="en">Lawrie C.H., Gal S., Dunlop H.M. et al. (2008). Detection of elevated levels of tumour-associated microRNAs in serum of patients with diffuse large B-cell lymphoma. Br. J. Haematol., 141 (5), 672–675. doi: 10.1111/j.1365-2141.2008.07077.x.</mixed-citation></citation-alternatives></ref><ref id="cit133"><label>133</label><citation-alternatives><mixed-citation xml:lang="ru">Cui B., Chen L., Zhang S. et al. MicroRNA-155 influences B-cell receptor signaling and associates with aggressive disease in chronic lymphocytic leukemia // Blood. 2014. Vol. 124 (4). P. 546–554. doi: 10.1182/blood-2014-03-559690.</mixed-citation><mixed-citation xml:lang="en">Cui B., Chen L., Zhang S. et al. (2014). MicroRNA-155 influences B-cell receptor signaling and associates with aggressive disease in chronic lymphocytic leukemia. Blood, 124 (4), 546–554. doi: 10.1182/blood-2014-03-559690.</mixed-citation></citation-alternatives></ref><ref id="cit134"><label>134</label><citation-alternatives><mixed-citation xml:lang="ru">Mraz M., Chen L., Rassenti L.Z. et al. miR-150 influences B-cell receptor signaling in chronic lymphocytic leukemia by regulating expression of GAB1 and FOXP1 // Blood. 2014. Vol. 124 (1). P. 84–95. doi: 10.1182/blood-2013-09-527234.</mixed-citation><mixed-citation xml:lang="en">Mraz M., Chen L., Rassenti L.Z. et al. (2014). miR-150 influences B-cell receptor signaling in chronic lymphocytic leukemia by regulating expression of GAB1 and FOXP1. Blood, 124 (1), 84–95. doi: 10.1182/blood-2013-09-527234.</mixed-citation></citation-alternatives></ref><ref id="cit135"><label>135</label><citation-alternatives><mixed-citation xml:lang="ru">Klein U., Lia M., Crespo M. et al. The DLEU2/miR- 15a/16-1 cluster controls B cell proliferation and its deletion leads to chronic lymphocytic leukemia // Cancer Cell. 2010. Vol. 17 (1). P. 28–40. doi: 10.1016/j.ccr.2009.11.019.</mixed-citation><mixed-citation xml:lang="en">Klein U., Lia M., Crespo M. et al. (2010). The DLEU2/ miR-15a/16-1 cluster controls B cell proliferation and its deletion leads to chronic lymphocytic leukemia. Cancer Cell, 17 (1), 28–40. doi: 10.1016/j.ccr.2009.11.019.</mixed-citation></citation-alternatives></ref><ref id="cit136"><label>136</label><citation-alternatives><mixed-citation xml:lang="ru">Di Lisio L., Gómez-López G., Sánchez-Beato M. et al. Mantle cell lymphoma: transcriptional regulation by microRNAs // Leukemia. 2010. Vol. 24 (7). P. 1335– 1342. doi: 10.1038/leu.2010.91.</mixed-citation><mixed-citation xml:lang="en">Di Lisio L., Gómez-López G., Sánchez-Beato M. et al. (2010). Mantle cell lymphoma: transcriptional regulation by microRNAs. Leukemia, 24 (7), 1335–1342. doi: 10.1038/leu.2010.91.</mixed-citation></citation-alternatives></ref><ref id="cit137"><label>137</label><citation-alternatives><mixed-citation xml:lang="ru">Zhao J.J., Lin J., Lwin T. et al. microRNA expression profile and identification of miR-29 as a prognostic marker and pathogenetic factor by targeting CDK6 in mantle cell lymphoma // Blood. 2010. Vol. 115 (13). P. 2630–2639. doi: 10.1182/blood-2009-09-243147.</mixed-citation><mixed-citation xml:lang="en">Zhao J.J., Lin J., Lwin T. et al. (2010). MicroRNA expression profile and identification of miR-29 as a prognostic marker and pathogenetic factor by targeting CDK6 in mantle cell lymphoma. Blood, 115 (13), 2630–2639. doi: 10.1182/blood-2009-09-243147.</mixed-citation></citation-alternatives></ref><ref id="cit138"><label>138</label><citation-alternatives><mixed-citation xml:lang="ru">Mraz M., Malinova K., Kotaskova J. et al. miR-34a, miR-29c and miR-17-5p are downregulated in CLL patients with TP53 abnormalities // Leukemia. 2009. Vol. 23 (6). P. 1159–1163. doi: 10.1038/leu.2008.377.</mixed-citation><mixed-citation xml:lang="en">Mraz M., Malinova K., Kotaskova J. et al. (2009). miR-34a, miR-29c and miR-17-5p are downregulated in CLL patients with TP53 abnormalities. Leukemia, 23 (6), 1159–1163. doi: 10.1038/leu.2008.377.</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
