<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.3 20210610//EN" "JATS-journalpublishing1-3.dtd">
<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">surgonco</journal-id><journal-title-group><journal-title xml:lang="ru">Креативная хирургия и онкология</journal-title><trans-title-group xml:lang="en"><trans-title>Creative surgery and oncology</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2076-3093</issn><issn pub-type="epub">2307-0501</issn><publisher><publisher-name>Башкирский государственный медицинский университет</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.24060/2076-3093-2026-16-1-34-42</article-id><article-id custom-type="elpub" pub-id-type="custom">surgonco-1177</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>ОБЗОР ЛИТЕРАТУРЫ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>REVIEWS</subject></subj-group></article-categories><title-group><article-title>Молекулярные регуляторы стволовости и лекарственной резистентности рака предстательной железы: роли MUC1‑C, TMPRSS4, TLX и MDA‑9/Syntenin</article-title><trans-title-group xml:lang="en"><trans-title>Molecular Regulators of Stemness and Drug Resistance in Prostate Cancer: Roles of MUC1‑C, TMPRSS4, TLX, and MDA‑9/Syntenin</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0003-7673-1766</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Шаяхметов</surname><given-names>Р. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Shayakhmetov</surname><given-names>R. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Шаяхметов Рустам Ильгизович — младший научный сотрудник, лаборатория стволовых клеток.</p><p>Республика Башкортостан, Уфа</p></bio><bio xml:lang="en"><p>Rustam I. Shayakhmetov — Junior Researcher, Stem Cells Laboratory.</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0007-7467-5034</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ле</surname><given-names>Т. Ч.</given-names></name><name name-style="western" xml:lang="en"><surname>Le</surname><given-names>Thu Chang</given-names></name></name-alternatives><bio xml:lang="ru"><p>Ле Тху Чанг — к.б.н., старший научный сотрудник, лаборатория стволовых клеток.</p><p>Республика Башкортостан, Уфа</p></bio><bio xml:lang="en"><p>Thu Chang Le — Cand. Sci. (Biol.), Senior Researcher, Stem Cells Laboratory.</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-9393-2875</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ишметова</surname><given-names>Д. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Ishmetova</surname><given-names>D. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Ишметова Диана Валиевна — младший научный сотрудник, лаборатория столовых клеток.</p><p>Республика Башкортостан, Уфа</p></bio><bio xml:lang="en"><p>Diana V. Ishmetova — Junior Researcher, Stem Cells Laboratory.</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0009-8191-9951</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Рахматуллина</surname><given-names>А. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Rakhmatullina</surname><given-names>A. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Рахматуллина Аида Ильдаровна — лаборант-исследователь, лаборатория стволовых клеток.</p><p>Республика Башкортостан, Уфа</p></bio><bio xml:lang="en"><p>Aida I. Rakhmatullina — Laboratory Research Assistant, Stem Cells Laboratory.</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-0882-7048</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Кагирова</surname><given-names>Э. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Kagirova</surname><given-names>E. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Кагирова Эвелина Марсельевна — к.б.н., старший научный сотрудник, лаборатория молекулярной генетики.</p><p>Республика Башкортостан, Уфа</p></bio><bio xml:lang="en"><p>Evelina M. Kagirova — Cand. Sci. (Biol.), Senior Researcher, Molecular Genetics Laboratory.</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-4911-8037</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Асадуллина</surname><given-names>Д. Д.</given-names></name><name name-style="western" xml:lang="en"><surname>Asadullina</surname><given-names>D. D.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Асадуллина Дилара Динаровна — младший научный сотрудник, лаборатория молекулярной генетики.</p><p>Республика Башкортостан, Уфа</p></bio><bio xml:lang="en"><p>Dilara D. Asadullina — Junior Researcher, Molecular Genetics Laboratory.</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-6812-9570</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Мухамадеев</surname><given-names>Р. Р.</given-names></name><name name-style="western" xml:lang="en"><surname>Mukhamadeev</surname><given-names>R. R.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Мухамадеев Радмир Радикович — лаборатория молекулярной генетики.</p><p>Республика Башкортостан, Уфа</p></bio><bio xml:lang="en"><p>Radmir R. Mukhamadeev — Molecular Genetics Laboratory</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-8381-2850</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ибатуллин</surname><given-names>А. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Ibatullin</surname><given-names>A. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Ибатуллин Артур Альбертович — д.м.н., лаборатория стволовых клеток.</p><p>Республика Башкортостан, Уфа</p></bio><bio xml:lang="en"><p>Artur A. Ibatullin — Dr. Sci. (Med.), Stem Cells Laboratory.</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-2125-4897</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Павлов</surname><given-names>В. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Pavlov</surname><given-names>V. N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Павлов Валентин Николаевич — д.м.н., профессор, кафедра урологии и онкологии.</p><p>Республика Башкортостан, Уфа</p></bio><bio xml:lang="en"><p>Valentin N. Pavlov — Dr. Sci. (Med.), Prof., Department of Urology and Oncology.</p></bio><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Башкирский государственный медицинский университет</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Bashkir State Medical University</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2026</year></pub-date><pub-date pub-type="epub"><day>09</day><month>04</month><year>2026</year></pub-date><volume>16</volume><issue>1</issue><fpage>34</fpage><lpage>42</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Шаяхметов Р.И., Ле Т.Ч., Ишметова Д.В., Рахматуллина А.И., Кагирова Э.М., Асадуллина Д.Д., Мухамадеев Р.Р., Ибатуллин А.А., Павлов В.Н., 2026</copyright-statement><copyright-year>2026</copyright-year><copyright-holder xml:lang="ru">Шаяхметов Р.И., Ле Т.Ч., Ишметова Д.В., Рахматуллина А.И., Кагирова Э.М., Асадуллина Д.Д., Мухамадеев Р.Р., Ибатуллин А.А., Павлов В.Н.</copyright-holder><copyright-holder xml:lang="en">Shayakhmetov R.I., Le T., Ishmetova D.V., Rakhmatullina A.I., Kagirova E.M., Asadullina D.D., Mukhamadeev R.R., Ibatullin A.A., Pavlov 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://www.surgonco.ru/jour/article/view/1177">https://www.surgonco.ru/jour/article/view/1177</self-uri><abstract><p>Рак предстательной железы (РПЖ) остается одним из самых распространенных злокачественных новообразований у мужчин и одной из ведущих причин онкологической смертности, особенно на стадиях кастрационно-резистентного и метастатического течения заболевания. Накопленные данные свидетельствуют о ключевой роли популяции опухолевых стволовых клеток в инициации опухолевого роста, прогрессии, формировании внутриопухолевой гетерогенности, лекарственной и радиорезистентности РПЖ. В обзоре суммированы сведения и детально рассмотрены четыре перспективных регулятора стволовости и пластичности опухолевых клеток: онкобелок MUC1-C, трансмембранная сериновая протеаза TMPRSS4, орфанный ядерный рецептор TLX и адаптерный PDZ-белок MDA-9/Syntenin. Для каждого из этих молекулярных факторов обсуждаются структура, особенности экспрессии в ткани простаты, участие в ключевых сигнальных путях (Wnt/β-catenin, PI3K/AKT, MAPK, STAT3, NOTCH, TGF-β и др.), а также их вклад в эпителиально-мезенхимальный переход, поддержание ОСК-фенотипа, андроген-независимый рост и резистентность к стандартным видам терапии. Особое внимание уделено данным in vitro и in vivo, подтверждающим значимость MUC1-C, TMPRSS4, TLX и MDA-9/Syntenin как потенциальных биомаркеров неблагоприятного течения РПЖ и мишеней для таргетной и иммунотерапии.</p></abstract><trans-abstract xml:lang="en"><p>Prostate cancer (PCa) remains one of the most prevalent malignancies in men and a leading cause of cancer-related mortality, particularly in its castration-resistant and metastatic forms. Accumulating evidence highlights the central role of cancer stem cells (CSCs) in tumor initiation, progression, intratumoral heterogeneity, and the resistance to therapy and radiation. This review summarizes current data and provides an in-depth analysis of four promossing regulators of CSC-associated stemness and cellular plasticity: the oncoprotein MUC1-C, the type II transmembrane serine protease TMPRSS4, the orphan nuclear receptor TLX, and the PDZ-domain adaptor protein MDA-9/Syntenin. For each molecule, we discuss structural features, expression patterns in prostate tissue, and involvement in key oncogenic signaling pathways, including Wnt/β-catenin, PI3K/AKT, MAPK, STAT3, NOTCH, and TGF-β. Their contributions to epithelial-mesenchymal transition (EMT), maintenance of the CSC phenotype, androgen-independent growth, and resistance to standard therapies are examined in detail. Particular emphasis is placed on in vitro and in vivo evidence demonstrating the significance of MUC1-C, TMPRSS4, TLX, and MDA-9/syntenin as biomarkers of aggressive PCa and as targets for precision therapeutics and immunotherapy.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>рак простаты</kwd><kwd>кастрационно-резистентные новообразования предстательной железы</kwd><kwd>опухолевые стволовые клетки</kwd><kwd>терапия</kwd><kwd>сигнальный путь</kwd><kwd>биомаркеры</kwd></kwd-group><kwd-group xml:lang="en"><kwd>prostate cancer</kwd><kwd>castration-resistant prostate cancer</kwd><kwd>cancer stem cells</kwd><kwd>therapy</kwd><kwd>signaling pathway</kwd><kwd>biomarkers</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Работа выполнена за счет средств Программы стратегического академического лидерства Башкирского государственного медицинского университета (ПРИОРИТЕТ-2030)</funding-statement><funding-statement xml:lang="en">This work was supported by the Bashkir State Medical University Strategic Academic Leadership Program (PRIORITY-2030)</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">Каприн А.Д., Старинский В.В., Петрова Г.В. (ред.) Злокачественные новообразования в России в 2017 году (заболеваемость и смертность). М., 2018.</mixed-citation><mixed-citation xml:lang="en">Kaprin A.D., Starinsky V.V., Petrova G.V. (ed.) Malignant neoplasms in Russia in 2017 (morbidity and mortality). Мoscow, 2018. (In Russ.).</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Bray F., Laversanne M., Sung H., Ferlay J., Siegel R.L., Soerjomataram I., et al. Global cancer statistics 2022: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2024;74(3):229–63. DOI: 10.3322/caac.21834</mixed-citation><mixed-citation xml:lang="en">Bray F., Laversanne M., Sung H., Ferlay J., Siegel R.L., Soerjomataram I., et al. Global cancer statistics 2022: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2024;74(3):229–63. DOI: 10.3322/caac.21834</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Zhou K., Lu H., Zhang J., Shen Q., Liu P., Xu Q., et al. Prostate cancer stem cells: an updated mini-review. J Cancer. 2024;15(20):6570–6. DOI: 10.7150/jca.100604</mixed-citation><mixed-citation xml:lang="en">Zhou K., Lu H., Zhang J., Shen Q., Liu P., Xu Q., et al. Prostate cancer stem cells: an updated mini-review. J Cancer. 2024;15(20):6570–6. DOI: 10.7150/jca.100604</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Омельчук Е.П., Кутилин Д.С., Димитриадис С.Н., Гусарева М.А., Тимошкина Н.Н. Молекулярные и генетические аспекты радиорезистентности рака простаты. Бюллетень Сибирской медицины. 2021;20(3):182–92. DOI: 10.20538/1682-0363-20213-182-192</mixed-citation><mixed-citation xml:lang="en">Omelchuk E.P., Kutilin D.S., Dimitriadi S.N., Gusarev M.A., Timoshkina N.N. Molecular genetic aspects of prostate cancer radioresistance. Bulletin of Siberian Medicine. 2021;20(3):182–92 (In Russ.). DOI: 10.20538/1682-0363-2021-3-182-192</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Penning T.M. Dehydroepiandrosterone (DHEA)-SO4 depot and castration-resistant prostate cancer. Vitam Horm. 2018;108:309–31. DOI: 10.1016/bs.vh.2018.01.007</mixed-citation><mixed-citation xml:lang="en">Penning T.M. Dehydroepiandrosterone (DHEA)-SO4 depot and castration-resistant prostate cancer. Vitam Horm. 2018;108:309–31. DOI: 10.1016/bs.vh.2018.01.007</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Nyquist M.D., Corella A., Coleman I., De Sarkar N., Kaipainen A., Ha G., et al. Combined TP53 and RB1 loss promotes prostate cancer resistance to a spectrum of therapeutics and confers vul-nerability to replication stress. Cell Rep. 2020;31(8):107669. DOI: 10.1016/j.celrep.2020.107669</mixed-citation><mixed-citation xml:lang="en">Nyquist M.D., Corella A., Coleman I., De Sarkar N., Kaipainen A., Ha G., et al. Combined TP53 and RB1 loss promotes prostate cancer resistance to a spectrum of therapeutics and confers vul-nerability to replication stress. Cell Rep. 2020;31(8):107669. DOI: 10.1016/j.celrep.2020.107669</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Lumahan L.E.V., Arif M., Whitener A.E., Yi P. Regulating androgen receptor function in prostate cancer: exploring the diversity of post-translational modifications. Cells. 2024;13(2):191. DOI: 10.3390/cells13020191</mixed-citation><mixed-citation xml:lang="en">Lumahan L.E.V., Arif M., Whitener A.E., Yi P. Regulating androgen receptor function in prostate cancer: exploring the diversity of post-translational modifications. Cells. 2024;13(2):191. DOI: 10.3390/cells13020191</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Pan Y., Yuan C., Zeng C., Sun C., Xia L., Wang G., et al. Cancer stem cells and niches: challenges in immunotherapy resistance. Mol Cancer. 2025;24(1):52. DOI: 10.1186/s12943-025-02265-2</mixed-citation><mixed-citation xml:lang="en">Pan Y., Yuan C., Zeng C., Sun C., Xia L., Wang G., et al. Cancer stem cells and niches: challenges in immunotherapy resistance. Mol Cancer. 2025;24(1):52. DOI: 10.1186/s12943-025-02265-2</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Lee H., Kim B., Park J., Park S., Yoo G., Yum S., et al. Cancer stem cells: landscape, challenges and emerging therapeutic innovations. Signal Transduct Target Ther. 2025;10(1):248. DOI: 10.1038/s41392-025-02360-2</mixed-citation><mixed-citation xml:lang="en">Lee H., Kim B., Park J., Park S., Yoo G., Yum S., et al. Cancer stem cells: landscape, challenges and emerging therapeutic innovations. Signal Transduct Target Ther. 2025;10(1):248. DOI: 10.1038/s41392-025-02360-2</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Yuan H., Qiu Y., Mei Z., Liu J., Wang L., Zhang K., et al. Cancer stem cells and tumor-associated macrophages: Interactions and therapeutic opportunities. Cancer Lett. 2025;624:217737. DOI: 10.1016/j.canlet.2025.217737</mixed-citation><mixed-citation xml:lang="en">Yuan H., Qiu Y., Mei Z., Liu J., Wang L., Zhang K., et al. Cancer stem cells and tumor-associated macrophages: Interactions and therapeutic opportunities. Cancer Lett. 2025;624:217737. DOI: 10.1016/j.canlet.2025.217737</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Wang H., Li J., Du F., Deng H. Cancer stem cells: Bridging microenvironmental interactions and clinical therapy. Clin Transl Med. 2025;15(7):e70406. DOI: 10.1002/ctm2.70406</mixed-citation><mixed-citation xml:lang="en">Wang H., Li J., Du F., Deng H. Cancer stem cells: Bridging microenvironmental interactions and clinical therapy. Clin Transl Med. 2025;15(7):e70406. DOI: 10.1002/ctm2.70406</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Haddadin L., Sun X. Stem cells in cancer: from mechanisms to therapeutic strategies. Cells. 2025;14(7):538. DOI: 10.3390/cells14070538</mixed-citation><mixed-citation xml:lang="en">Haddadin L., Sun X. Stem cells in cancer: from mechanisms to therapeutic strategies. Cells. 2025;14(7):538. DOI: 10.3390/cells14070538</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Tong X., Dong C., Liang S. Mucin1 as a potential molecule for cancer immunotherapy and targeted therapy. J Cancer. 2024;15(1):54–67. DOI: 10.7150/jca.88261</mixed-citation><mixed-citation xml:lang="en">Tong X., Dong C., Liang S. Mucin1 as a potential molecule for cancer immunotherapy and targeted therapy. J Cancer. 2024;15(1):54–67. DOI: 10.7150/jca.88261</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Radziejewska I. The role of MUC1 in gastric cancer development. Cancers (Basel). 2025;17(20):3331. DOI: 10.3390/cancers17203331</mixed-citation><mixed-citation xml:lang="en">Radziejewska I. The role of MUC1 in gastric cancer development. Cancers (Basel). 2025;17(20):3331. DOI: 10.3390/cancers17203331</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Hikita S.T., Kosik K.S., Clegg D.O., Bamdad C. MUC1* mediates the growth of human pluripotent stem cells. PLoS One. 2008;3(10):e3312. DOI: 10.1371/journal.pone.0003312</mixed-citation><mixed-citation xml:lang="en">Hikita S.T., Kosik K.S., Clegg D.O., Bamdad C. MUC1* mediates the growth of human pluripotent stem cells. PLoS One. 2008;3(10):e3312. DOI: 10.1371/journal.pone.0003312</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Park J.A., Park S., Park H.B., Han M.K., Lee Y. MUC1-C Contributes to the maintenance of human embryonic stem cells and promotes somatic cell reprogramming. Stem Cells Dev. 2021;30(21):1082–91. DOI: 10.1089/scd.2021.0185</mixed-citation><mixed-citation xml:lang="en">Park J.A., Park S., Park H.B., Han M.K., Lee Y. MUC1-C Contributes to the maintenance of human embryonic stem cells and promotes somatic cell reprogramming. Stem Cells Dev. 2021;30(21):1082–91. DOI: 10.1089/scd.2021.0185</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Lapointe J., Li C., Higgins J.P., Van de Rijn M., Bair E., Montgomery K., et al. Gene expression profiling identifies clinically relevant subtypes of prostate cancer. Proc Natl Acad Sci U S A. 2004;101(3):811–6. DOI: 10.1073/pnas.0304146101</mixed-citation><mixed-citation xml:lang="en">Lapointe J., Li C., Higgins J.P., Van de Rijn M., Bair E., Montgomery K., et al. Gene expression profiling identifies clinically relevant subtypes of prostate cancer. Proc Natl Acad Sci U S A. 2004;101(3):811–6. DOI: 10.1073/pnas.0304146101</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Kufe D. Dependence on MUC1-C in progression of neuroendocrine prostate cancer. Int J Mol Sci. 2023;24(4):3719. DOI: 10.3390/ijms24043719</mixed-citation><mixed-citation xml:lang="en">Kufe D. Dependence on MUC1-C in progression of neuroendocrine prostate cancer. Int J Mol Sci. 2023;24(4):3719. DOI: 10.3390/ijms24043719</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Shigeta K., Daimon T., Hongo H., Ku S.Y., Ozawa H., Haratake N., et al. MUC1-C dependence in treatment-resistant prostate cancer uncovers a target for antibody-drug conjugate therapy. JCI Insight. 2025;10(14):e190924. DOI: 10.1172/jci.insight.190924</mixed-citation><mixed-citation xml:lang="en">Shigeta K., Daimon T., Hongo H., Ku S.Y., Ozawa H., Haratake N., et al. MUC1-C dependence in treatment-resistant prostate cancer uncovers a target for antibody-drug conjugate therapy. JCI Insight. 2025;10(14):e190924. DOI: 10.1172/jci.insight.190924</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Nath S., Mukherjee P. MUC1: a multifaceted oncoprotein with a key role in cancer progression. Trends Mol Med. 2014;20(6):332–42. DOI: 10.1016/j.molmed.2014.02.007</mixed-citation><mixed-citation xml:lang="en">Nath S., Mukherjee P. MUC1: a multifaceted oncoprotein with a key role in cancer progression. Trends Mol Med. 2014;20(6):332–42. DOI: 10.1016/j.molmed.2014.02.007</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Yamashita N., Long M., Fushimi A., Yamamoto M., Hata T., Hagiwara M., et al. MUC1-C integrates activation of the IFN-γ pathway with suppression of the tumor immune microenvironment in triple-negative breast cancer. J Immunother Cancer. 2021;9(1):e002115. DOI: 10.1136/jitc-2020-002115</mixed-citation><mixed-citation xml:lang="en">Yamashita N., Long M., Fushimi A., Yamamoto M., Hata T., Hagiwara M., et al. MUC1-C integrates activation of the IFN-γ pathway with suppression of the tumor immune microenvironment in triple-negative breast cancer. J Immunother Cancer. 2021;9(1):e002115. DOI: 10.1136/jitc-2020-002115</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Altschuler Y., Kinlough C.L., Poland P.A., Bruns J.B., Apodaca G., Weisz O.A., et al. Clathrin-mediated endocytosis of MUC1 is modulated by its glycosylation state. Mol Biol Cell. 2000;11(3):819–31. DOI: 10.1091/mbc.11.3.819</mixed-citation><mixed-citation xml:lang="en">Altschuler Y., Kinlough C.L., Poland P.A., Bruns J.B., Apodaca G., Weisz O.A., et al. Clathrin-mediated endocytosis of MUC1 is modulated by its glycosylation state. Mol Biol Cell. 2000;11(3):819–31. DOI: 10.1091/mbc.11.3.819</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Караулов А.В., Гурина Н.Н., Новиков Д.В., Фомина С.Г., Новиков В.В. Роль экспрессии белка muc1 в прогрессии опухоли. Вестник РАМН. 2016;71(5):392–6. DOI: 10.15690/vramn736</mixed-citation><mixed-citation xml:lang="en">Karaulov A.V., Gurina N.N., Novikov D.V., Fomina S.G., Novikov V.V. Role of MUC1 expression in tumor progression. Annals of the Russian academy of medical sciences. 2016;71(5):392–6. (In Russ.). DOI: 10.15690/vramn736</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Hagiwara M., Yasumizu Y., Yamashita N., Rajabi H., Fushimi A., Long M.D., et al. MUC1-C activates the BAF (mSWI/SNF) complex in prostate cancer stem cells. Cancer Res. 2021;81(4):1111–22. DOI: 10.1158/0008-5472.CAN-20-2588</mixed-citation><mixed-citation xml:lang="en">Hagiwara M., Yasumizu Y., Yamashita N., Rajabi H., Fushimi A., Long M.D., et al. MUC1-C activates the BAF (mSWI/SNF) complex in prostate cancer stem cells. Cancer Res. 2021;81(4):1111–22. DOI: 10.1158/0008-5472.CAN-20-2588</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Kufe D.W. Mucins in cancer: function, prognosis and therapy. Nat Rev Cancer. 2009;9(12):874–85. DOI: 10.1038/nrc2761</mixed-citation><mixed-citation xml:lang="en">Kufe D.W. Mucins in cancer: function, prognosis and therapy. Nat Rev Cancer. 2009;9(12):874–85. DOI: 10.1038/nrc2761</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Wan X., Liu J., Lu J.F., Tzelepi V., Yang J., Starbuck M.W., et al. Activation of β-catenin signaling in androgen receptor-negative prostate cancer cells. Clin Cancer Res. 2012;18(3):726–36. DOI: 10.1158/1078-0432.CCR-11-2521</mixed-citation><mixed-citation xml:lang="en">Wan X., Liu J., Lu J.F., Tzelepi V., Yang J., Starbuck M.W., et al. Activation of β-catenin signaling in androgen receptor-negative prostate cancer cells. Clin Cancer Res. 2012;18(3):726–36. DOI: 10.1158/1078-0432.CCR-11-2521</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Kufe D.W. MUC1-C oncoprotein as a target in breast cancer: activation of signaling pathways and therapeutic approaches. Oncogene. 2013;32(9):1073–81. DOI: 10.1038/onc.2012.158</mixed-citation><mixed-citation xml:lang="en">Kufe D.W. MUC1-C oncoprotein as a target in breast cancer: activation of signaling pathways and therapeutic approaches. Oncogene. 2013;32(9):1073–81. DOI: 10.1038/onc.2012.158</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Kim S. TMPRSS4, a type II transmembrane serine protease, as a potential therapeutic target in cancer. Exp Mol Med. 2023;55(4):716–24. DOI: 10.1038/s12276-023-00975-5</mixed-citation><mixed-citation xml:lang="en">Kim S. TMPRSS4, a type II transmembrane serine protease, as a potential therapeutic target in cancer. Exp Mol Med. 2023;55(4):716–24. DOI: 10.1038/s12276-023-00975-5</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Shi G., Yang X., Dai B., Zhang H., Shen Y., Zhu Y., et al. Clinical significance of TMPRSS4 in prostate cancer. Int J Clin Exp Pathol. 2014;7(11):8053–8. PMID: 25550850</mixed-citation><mixed-citation xml:lang="en">Shi G., Yang X., Dai B., Zhang H., Shen Y., Zhu Y., et al. Clinical significance of TMPRSS4 in prostate cancer. Int J Clin Exp Pathol. 2014;7(11):8053–8. PMID: 25550850</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Yang Y.S., Wen D., Zhao X.F. Transmembrane protease TMPRSS4 promotes the formation and development of mismatch repair deficient colon cancer liver metastasis. Bull Exp Biol Med. 2021 May;171(2):242–6. DOI: 10.1007/s10517-021-05203-6. Erratum in: Bull Exp Biol Med. 2021;172(1):112. DOI: 10.1007/s10517-021-05343-9</mixed-citation><mixed-citation xml:lang="en">Yang Y.S., Wen D., Zhao X.F. Transmembrane protease TMPRSS4 promotes the formation and development of mismatch repair deficient colon cancer liver metastasis. Bull Exp Biol Med. 2021 May;171(2):242–6. DOI: 10.1007/s10517-021-05203-6. Erratum in: Bull Exp Biol Med. 2021;172(1):112. DOI: 10.1007/s10517-021-05343-9</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Min H.J., Lee Y., Zhao X.F., Park Y.K., Lee M.K., Lee J.W., et al. TMPRSS4 upregulates uPA gene expression through JNK signaling activation to induce cancer cell invasion. Cell Signal. 2014;26(2):398–408. DOI: 10.1016/j.cellsig.2013.08.002</mixed-citation><mixed-citation xml:lang="en">Min H.J., Lee Y., Zhao X.F., Park Y.K., Lee M.K., Lee J.W., et al. TMPRSS4 upregulates uPA gene expression through JNK signaling activation to induce cancer cell invasion. Cell Signal. 2014;26(2):398–408. DOI: 10.1016/j.cellsig.2013.08.002</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Jung H., Lee K.P., Park S.J., Park J.H., Jang Y.S., Choi S.Y., et al. TMPRSS4 promotes invasion, migration and metastasis of human tumor cells by facilitating an epithelial-mesenchymal transition. Oncogene. 2008;27(18):2635–47. DOI: 10.1038/sj.onc.1210914</mixed-citation><mixed-citation xml:lang="en">Jung H., Lee K.P., Park S.J., Park J.H., Jang Y.S., Choi S.Y., et al. TMPRSS4 promotes invasion, migration and metastasis of human tumor cells by facilitating an epithelial-mesenchymal transition. Oncogene. 2008;27(18):2635–47. DOI: 10.1038/sj.onc.1210914</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Lee Y., Ko D., Min H.J., Kim S.B., Ahn H.M., Lee Y., et al. TMPRSS4 induces invasion and proliferation of prostate cancer cells through induction of Slug and cyclin D1. Oncotarget. 2016;7(31):50315–32. DOI: 10.18632/oncotarget.10382</mixed-citation><mixed-citation xml:lang="en">Lee Y., Ko D., Min H.J., Kim S.B., Ahn H.M., Lee Y., et al. TMPRSS4 induces invasion and proliferation of prostate cancer cells through induction of Slug and cyclin D1. Oncotarget. 2016;7(31):50315–32. DOI: 10.18632/oncotarget.10382</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Lee Y., Yoon J., Ko D., Yu M., Lee S., Kim S. TMPRSS4 promotes cancer stem-like properties in prostate cancer cells through upregulation of SOX2 by SLUG and TWIST1. J Exp Clin Cancer Res. 2021;40(1):372. DOI: 10.1186/s13046-021-02147-7</mixed-citation><mixed-citation xml:lang="en">Lee Y., Yoon J., Ko D., Yu M., Lee S., Kim S. TMPRSS4 promotes cancer stem-like properties in prostate cancer cells through upregulation of SOX2 by SLUG and TWIST1. J Exp Clin Cancer Res. 2021;40(1):372. DOI: 10.1186/s13046-021-02147-7</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Nelson A.T., Wang Y., Nelson E.R. TLX, an orphan nuclear receptor with emerging roles in physiology and disease. Endocrinology. 2021;162(11):bqab184. DOI: 10.1210/endocr/bqab184</mixed-citation><mixed-citation xml:lang="en">Nelson A.T., Wang Y., Nelson E.R. TLX, an orphan nuclear receptor with emerging roles in physiology and disease. Endocrinology. 2021;162(11):bqab184. DOI: 10.1210/endocr/bqab184</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Liu H.K., Wang Y., Belz T., Bock D., Takacs A., Radlwimmer B., et al. The nuclear receptor tailless induces long-term neural stem cell expansion and brain tumor initiation. Genes Dev. 2010;24:683–95. DOI: 10.1101/gad.560310</mixed-citation><mixed-citation xml:lang="en">Liu H.K., Wang Y., Belz T., Bock D., Takacs A., Radlwimmer B., et al. The nuclear receptor tailless induces long-term neural stem cell expansion and brain tumor initiation. Genes Dev. 2010;24:683–95. DOI: 10.1101/gad.560310</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Faudone G., Bischoff-Kont I., Rachor L., Willems S., Zhubi R., Kaiser A., et al. Propranolol activates the orphan nuclear receptor TLX to counteract proliferation and migration of glioblastoma cells. J Med Chem. 2021;64(12):8727–38. DOI: 10.1021/acs.jmedchem.1c00733</mixed-citation><mixed-citation xml:lang="en">Faudone G., Bischoff-Kont I., Rachor L., Willems S., Zhubi R., Kaiser A., et al. Propranolol activates the orphan nuclear receptor TLX to counteract proliferation and migration of glioblastoma cells. J Med Chem. 2021;64(12):8727–38. DOI: 10.1021/acs.jmedchem.1c00733</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Lin M.L., Patel H., Remenyi J., Banerji C.R., Lai C.F., Periyasamy M., et al. Expression profiling of nuclear receptors in breast cancer identifies TLX as a mediator of growth and invasion in triple-negative breast cancer. Oncotarget. 2015;6(25):21685–703. DOI: 10.18632/oncotarget.3942</mixed-citation><mixed-citation xml:lang="en">Lin M.L., Patel H., Remenyi J., Banerji C.R., Lai C.F., Periyasamy M., et al. Expression profiling of nuclear receptors in breast cancer identifies TLX as a mediator of growth and invasion in triple-negative breast cancer. Oncotarget. 2015;6(25):21685–703. DOI: 10.18632/oncotarget.3942</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Jia L., Wu D., Wang Y., You W., Wang Z., Xiao L., et al. Orphan nuclear receptor TLX contributes to androgen insensitivity in castration-resistant prostate cancer via its repression of androgen receptor transcription. Oncogene. 2018;37(25):3340–55. DOI: 10.1038/s41388-018-0198-z</mixed-citation><mixed-citation xml:lang="en">Jia L., Wu D., Wang Y., You W., Wang Z., Xiao L., et al. Orphan nuclear receptor TLX contributes to androgen insensitivity in castration-resistant prostate cancer via its repression of androgen receptor transcription. Oncogene. 2018;37(25):3340–55. DOI: 10.1038/s41388-018-0198-z</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Chow S.T., Fan J., Zhang X., Wang Y., Li Y., Ng C.F. Nuclear receptor TLX functions to promote cancer stemness and EMT in prostate cancer via its direct transactivation of CD44 and stem cell-regulatory transcription factors. Br J Cancer. 2024;131(9):1450–62. DOI: 10.1038/s41416-024-02843-z</mixed-citation><mixed-citation xml:lang="en">Chow S.T., Fan J., Zhang X., Wang Y., Li Y., Ng C.F. Nuclear receptor TLX functions to promote cancer stemness and EMT in prostate cancer via its direct transactivation of CD44 and stem cell-regulatory transcription factors. Br J Cancer. 2024;131(9):1450–62. DOI: 10.1038/s41416-024-02843-z</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Pintor-Romero V. G., Hurtado-Ortega E., Nicolás-Morales M. L., Gutiérrez-Torres M., Vences-Velázquez A., Ortuño-Pineda C., et al. Biological role and aberrant overexpression of syntenin-1 in cancer: potential role as a biomarker and therapeutic target. Biomedicines. 2023;11(4):1034. DOI: 10.3390/biomedicines11041034</mixed-citation><mixed-citation xml:lang="en">Pintor-Romero V. G., Hurtado-Ortega E., Nicolás-Morales M. L., Gutiérrez-Torres M., Vences-Velázquez A., Ortuño-Pineda C., et al. Biological role and aberrant overexpression of syntenin-1 in cancer: potential role as a biomarker and therapeutic target. Biomedicines. 2023;11(4):1034. DOI: 10.3390/biomedicines11041034</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Das S.K., Maji S., Wechman S.L., Bhoopathi P., Pradhan A.K., Talukdar S., et al. MDA-9/Syntenin (SDCBP): Novel gene and therapeutic target for cancer metastasis. Pharmacol Res. 2020; 155:104695. DOI: 10.1016/j.phrs.2020.104695</mixed-citation><mixed-citation xml:lang="en">Das S.K., Maji S., Wechman S.L., Bhoopathi P., Pradhan A.K., Talukdar S., et al. MDA-9/Syntenin (SDCBP): Novel gene and therapeutic target for cancer metastasis. Pharmacol Res. 2020; 155:104695. DOI: 10.1016/j.phrs.2020.104695</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Das S.K., Bhutia S.K., Kegelman T.P., Peachy L., Oyesanya R.A., Dasgupta S., et al. MDA-9/syntenin: a positive gatekeeper of melanoma metastasis. Front Biosci (Landmark Ed). 2012;17(1):1–15. DOI: 10.2741/3911</mixed-citation><mixed-citation xml:lang="en">Das S.K., Bhutia S.K., Kegelman T.P., Peachy L., Oyesanya R.A., Dasgupta S., et al. MDA-9/syntenin: a positive gatekeeper of melanoma metastasis. Front Biosci (Landmark Ed). 2012;17(1):1–15. DOI: 10.2741/3911</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Das S.K., Bhutia S.K., Azab B., Kegelman T.P., Peachy L., Santhekadur P.K., et al. MDA-9/syntenin and IGFBP-2 promote angiogenesis in human melanoma. Cancer Res. 2013;73(2):844–54. DOI: 10.1158/0008-5472.CAN-12-1681</mixed-citation><mixed-citation xml:lang="en">Das S.K., Bhutia S.K., Azab B., Kegelman T.P., Peachy L., Santhekadur P.K., et al. MDA-9/syntenin and IGFBP-2 promote angiogenesis in human melanoma. Cancer Res. 2013;73(2):844–54. DOI: 10.1158/0008-5472.CAN-12-1681</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Boukerche H., Su Z.Z., Prévot C., Sarkar D., Fisher P.B. Mda-9/Syntenin promotes metastasis in human melanoma cells by activating c-Src. Proc Natl Acad Sci U S A. 2008;105(41):15914–9. DOI: 10.1073/pnas.0808171105</mixed-citation><mixed-citation xml:lang="en">Boukerche H., Su Z.Z., Prévot C., Sarkar D., Fisher P.B. Mda-9/Syntenin promotes metastasis in human melanoma cells by activating c-Src. Proc Natl Acad Sci U S A. 2008;105(41):15914–9. DOI: 10.1073/pnas.0808171105</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Dasgupta S., Menezes M.E., Das S.K., Emdad L., Janjic A., Bhatia S. Novel role of MDA-9/syntenin in regulating urothelial cell proliferation by modulating EGFR signaling. Clin Cancer Res. 2013;19(17):4621–33. DOI: 10.1158/1078-0432.CCR-13-0585</mixed-citation><mixed-citation xml:lang="en">Dasgupta S., Menezes M.E., Das S.K., Emdad L., Janjic A., Bhatia S. Novel role of MDA-9/syntenin in regulating urothelial cell proliferation by modulating EGFR signaling. Clin Cancer Res. 2013;19(17):4621–33. DOI: 10.1158/1078-0432.CCR-13-0585</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">Koo T.H., Lee J.J., Kim E.M., Kim K.W., Kim H.D., Lee J.H. Syntenin is overexpressed and promotes cell migration in metastatic human breast and gastric cancer cell lines. Oncogene. 2002;21(26):4080–8. DOI: 10.1038/sj.onc.1205514</mixed-citation><mixed-citation xml:lang="en">Koo T.H., Lee J.J., Kim E.M., Kim K.W., Kim H.D., Lee J.H. Syntenin is overexpressed and promotes cell migration in metastatic human breast and gastric cancer cell lines. Oncogene. 2002;21(26):4080–8. DOI: 10.1038/sj.onc.1205514</mixed-citation></citation-alternatives></ref><ref id="cit48"><label>48</label><citation-alternatives><mixed-citation xml:lang="ru">Qian X.L., Li Y.Q., Yu B., Gu F., Liu F.F., Li W.D., et al. Syndecan binding protein (SDCBP) is overexpressed in estrogen receptor negative breast cancers, and is a potential promoter for tumor proliferation. PLoS One. 2013;8(3):e60046. DOI: 10.1371/journal.pone.0060046</mixed-citation><mixed-citation xml:lang="en">Qian X.L., Li Y.Q., Yu B., Gu F., Liu F.F., Li W.D., et al. Syndecan binding protein (SDCBP) is overexpressed in estrogen receptor negative breast cancers, and is a potential promoter for tumor proliferation. PLoS One. 2013;8(3):e60046. DOI: 10.1371/journal.pone.0060046</mixed-citation></citation-alternatives></ref><ref id="cit49"><label>49</label><citation-alternatives><mixed-citation xml:lang="ru">Menezes M.E., Shen X.N., Das S.K., Emdad L., Sarkar D., Fisher P.B. MDA-9/Syntenin (SDCBP) modulates small GTPases RhoA and Cdc42 via transforming growth factor β1 to enhance epithelial-mesenchymal transition in breast cancer. Oncotarget. 2016;7(49):80175–89. DOI: 10.18632/oncotarget.13373</mixed-citation><mixed-citation xml:lang="en">Menezes M.E., Shen X.N., Das S.K., Emdad L., Sarkar D., Fisher P.B. MDA-9/Syntenin (SDCBP) modulates small GTPases RhoA and Cdc42 via transforming growth factor β1 to enhance epithelial-mesenchymal transition in breast cancer. Oncotarget. 2016;7(49):80175–89. DOI: 10.18632/oncotarget.13373</mixed-citation></citation-alternatives></ref><ref id="cit50"><label>50</label><citation-alternatives><mixed-citation xml:lang="ru">Yu Y., Li S., Wang K., Wan X. A PDZ protein MDA-9/Syntenin: as a target for cancer therapy. Comput Struct Biotechnol J. 2019;17:136–41. DOI: 10.1016/j.csbj.2019.01.002</mixed-citation><mixed-citation xml:lang="en">Yu Y., Li S., Wang K., Wan X. A PDZ protein MDA-9/Syntenin: as a target for cancer therapy. Comput Struct Biotechnol J. 2019;17:136–41. DOI: 10.1016/j.csbj.2019.01.002</mixed-citation></citation-alternatives></ref><ref id="cit51"><label>51</label><citation-alternatives><mixed-citation xml:lang="ru">Wang L.K., Pan S.H., Chang Y.L., Hung P.F., Kao S.H., Wang W.L., et al. MDA-9/Syntenin-Slug transcriptional complex promote epithelial-mesenchymal transition and invasion/metastasis in lung adenocarcinoma. Oncotarget. 2016;7(1):386–401. DOI: 10.18632/oncotarget.6299</mixed-citation><mixed-citation xml:lang="en">Wang L.K., Pan S.H., Chang Y.L., Hung P.F., Kao S.H., Wang W.L., et al. MDA-9/Syntenin-Slug transcriptional complex promote epithelial-mesenchymal transition and invasion/metastasis in lung adenocarcinoma. Oncotarget. 2016;7(1):386–401. DOI: 10.18632/oncotarget.6299</mixed-citation></citation-alternatives></ref><ref id="cit52"><label>52</label><citation-alternatives><mixed-citation xml:lang="ru">Talukdar S., Das S.K., Pradhan A.K., Emdad L., Shen X.N., Windle J.J., et al. Novel function of MDA-9/Syntenin (SDCBP) as a regulator of survival and stemness in glioma stem cells. Oncotarget. 2016;7(34):54102–19. DOI: 10.18632/oncotarget.10851</mixed-citation><mixed-citation xml:lang="en">Talukdar S., Das S.K., Pradhan A.K., Emdad L., Shen X.N., Windle J.J., et al. Novel function of MDA-9/Syntenin (SDCBP) as a regulator of survival and stemness in glioma stem cells. Oncotarget. 2016;7(34):54102–19. DOI: 10.18632/oncotarget.10851</mixed-citation></citation-alternatives></ref><ref id="cit53"><label>53</label><citation-alternatives><mixed-citation xml:lang="ru">Talukdar S., Das S.K., Pradhan A.K., Emdad L., Windle J.J., Sarkar D., et al. MDA-9/Syntenin (SDCBP) is a critical regulator of chemoresistance, survival and stemness in prostate cancer stem cells. Cancers (Basel). 2019;12(1):53. DOI: 10.3390/cancers12010053</mixed-citation><mixed-citation xml:lang="en">Talukdar S., Das S.K., Pradhan A.K., Emdad L., Windle J.J., Sarkar D., et al. MDA-9/Syntenin (SDCBP) is a critical regulator of chemoresistance, survival and stemness in prostate cancer stem cells. Cancers (Basel). 2019;12(1):53. DOI: 10.3390/cancers12010053</mixed-citation></citation-alternatives></ref><ref id="cit54"><label>54</label><citation-alternatives><mixed-citation xml:lang="ru">Maji S., Pradhan A.K., Kumar A., Bhoopathi P., Mannangatti P., Guo C., et al. MDA-9/Syntenin in the tumor and microenvironment defines prostate cancer bone metastasis. Proc Natl Acad Sci U S A. 2023;120(45):e2307094120. DOI: 10.1073/pnas.2307094120</mixed-citation><mixed-citation xml:lang="en">Maji S., Pradhan A.K., Kumar A., Bhoopathi P., Mannangatti P., Guo C., et al. MDA-9/Syntenin in the tumor and microenvironment defines prostate cancer bone metastasis. Proc Natl Acad Sci U S A. 2023;120(45):e2307094120. DOI: 10.1073/pnas.2307094120</mixed-citation></citation-alternatives></ref><ref id="cit55"><label>55</label><citation-alternatives><mixed-citation xml:lang="ru">Das S.K., Pradhan A.K., Bhoopathi P., Talukdar S., Shen X.N., Sarkar D., et al. The MDA-9/Syntenin/IGF1R/STAT3 Axis directs prostate cancer invasion. Cancer Res. 2018;78(11):2852–63. DOI: 10.1158/0008-5472.CAN-17-2992</mixed-citation><mixed-citation xml:lang="en">Das S.K., Pradhan A.K., Bhoopathi P., Talukdar S., Shen X.N., Sarkar D., et al. The MDA-9/Syntenin/IGF1R/STAT3 Axis directs prostate cancer invasion. Cancer Res. 2018;78(11):2852–63. DOI: 10.1158/0008-5472.CAN-17-2992</mixed-citation></citation-alternatives></ref><ref id="cit56"><label>56</label><citation-alternatives><mixed-citation xml:lang="ru">Atawia I.M., Kushwaha P.P., Verma S., Lin S., Shankar E., Abdel-Gawad O., et al. Inhibition of Wnt/β-catenin pathway overcomes therapeutic resistance to abiraterone in castration-resistant prostate cancer. Mol Carcinog. 2023;62(9):1312–24. DOI: 10.1002/mc.23565</mixed-citation><mixed-citation xml:lang="en">Atawia I.M., Kushwaha P.P., Verma S., Lin S., Shankar E., Abdel-Gawad O., et al. Inhibition of Wnt/β-catenin pathway overcomes therapeutic resistance to abiraterone in castration-resistant prostate cancer. Mol Carcinog. 2023;62(9):1312–24. DOI: 10.1002/mc.23565</mixed-citation></citation-alternatives></ref><ref id="cit57"><label>57</label><citation-alternatives><mixed-citation xml:lang="ru">Liu Y.M., Wu A.D., Chen Y., Ma T.F., Dong B.Z., She Z.G., et al. Gastrodin inhibits prostate cancer proliferation by targeting canonical Wnt/β-catenin signaling pathway. Med Oncol. 2023;41(1):32. DOI: 10.1007/s12032-023-02254-9</mixed-citation><mixed-citation xml:lang="en">Liu Y.M., Wu A.D., Chen Y., Ma T.F., Dong B.Z., She Z.G., et al. Gastrodin inhibits prostate cancer proliferation by targeting canonical Wnt/β-catenin signaling pathway. Med Oncol. 2023;41(1):32. DOI: 10.1007/s12032-023-02254-9</mixed-citation></citation-alternatives></ref><ref id="cit58"><label>58</label><citation-alternatives><mixed-citation xml:lang="ru">Saito S., Ando K., Sakamoto S., Xu M., Yamada Y., Rii J., et al. The LAT1 inhibitor JPH203 suppresses the growth of castration-resistant prostate cancer through a CD24-mediated mechanism. Cancer Sci. 2024;115(7):2461–72. DOI: 10.1111/cas.16191</mixed-citation><mixed-citation xml:lang="en">Saito S., Ando K., Sakamoto S., Xu M., Yamada Y., Rii J., et al. The LAT1 inhibitor JPH203 suppresses the growth of castration-resistant prostate cancer through a CD24-mediated mechanism. Cancer Sci. 2024;115(7):2461–72. DOI: 10.1111/cas.16191</mixed-citation></citation-alternatives></ref><ref id="cit59"><label>59</label><citation-alternatives><mixed-citation xml:lang="ru">Lee M.H., Kundu J.K., Keum Y.S., Cho Y.Y., Surh Y.J., Choi B.Y. Resveratrol inhibits IL-6-induced transcriptional activity of AR and STAT3 in human prostate cancer LNCaP-FGC cells. Biomol Ther (Seoul). 2014;22(5):426–30. DOI: 10.4062/biomolther.2014.061</mixed-citation><mixed-citation xml:lang="en">Lee M.H., Kundu J.K., Keum Y.S., Cho Y.Y., Surh Y.J., Choi B.Y. Resveratrol inhibits IL-6-induced transcriptional activity of AR and STAT3 in human prostate cancer LNCaP-FGC cells. Biomol Ther (Seoul). 2014;22(5):426–30. DOI: 10.4062/biomolther.2014.061</mixed-citation></citation-alternatives></ref><ref id="cit60"><label>60</label><citation-alternatives><mixed-citation xml:lang="ru">Cao H., Feng Y., Sun P., Chen L., Wang D., Gao R. Zhoushi Qiling decoction inhibits proliferation of human prostate cancer cells through IL6/STAT3 pathway. J Cancer. 2023;14(12):2246–54. DOI: 10.7150/jca.84943</mixed-citation><mixed-citation xml:lang="en">Cao H., Feng Y., Sun P., Chen L., Wang D., Gao R. Zhoushi Qiling decoction inhibits proliferation of human prostate cancer cells through IL6/STAT3 pathway. J Cancer. 2023;14(12):2246–54. DOI: 10.7150/jca.84943</mixed-citation></citation-alternatives></ref><ref id="cit61"><label>61</label><citation-alternatives><mixed-citation xml:lang="ru">Cai F., Guo S., Huang S., Li J., Liu W. Rubimaillin suppresses proliferation, migration and invasion of prostate cancer cells via the Notch-1/MMP signaling pathway. Cell Mol Biol (Noisy-le-grand). 2020;66(2):130–4. PMID: 32415939</mixed-citation><mixed-citation xml:lang="en">Cai F., Guo S., Huang S., Li J., Liu W. Rubimaillin suppresses proliferation, migration and invasion of prostate cancer cells via the Notch-1/MMP signaling pathway. Cell Mol Biol (Noisy-le-grand). 2020;66(2):130–4. PMID: 32415939</mixed-citation></citation-alternatives></ref><ref id="cit62"><label>62</label><citation-alternatives><mixed-citation xml:lang="ru">Cai M., Ge S., Hong Y., Chen Y., Ren Y.Z., Zhong D., et al. Tegaserod maleate exerts anti-tumor effects on prostate cancer via repressing sonic hedgehog signaling pathway. Mol Med. 2025;31(1):30. DOI: 10.1186/s10020-025-01080-1</mixed-citation><mixed-citation xml:lang="en">Cai M., Ge S., Hong Y., Chen Y., Ren Y.Z., Zhong D., et al. Tegaserod maleate exerts anti-tumor effects on prostate cancer via repressing sonic hedgehog signaling pathway. Mol Med. 2025;31(1):30. DOI: 10.1186/s10020-025-01080-1</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>
