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<article 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" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="review-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Molecular Biology</journal-id><journal-title-group><journal-title xml:lang="en">Molecular Biology</journal-title><trans-title-group xml:lang="ru"><trans-title>Молекулярная биология</trans-title></trans-title-group></journal-title-group><issn publication-format="print">0026-8984</issn><issn publication-format="electronic">3034-5553</issn><publisher><publisher-name xml:lang="en">The Russian Academy of Sciences</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">699674</article-id><article-id pub-id-type="doi">10.7868/S3034555325060029</article-id><article-categories><subj-group subj-group-type="toc-heading"><subject>ОБЗОРЫ</subject></subj-group><subj-group subj-group-type="article-type"><subject>Review Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Gut microbiota in Colorectal Cancer Carcinogenesis: Evolution of Hypotheses</article-title><trans-title-group xml:lang="ru"><trans-title>КИШЕЧНАЯ МИКРОБИОТА В КАНЦЕРОГЕНЕЗЕ КОЛОРЕКТАЛЬНОГО РАКА: ЭВОЛЮЦИЯ ГИПОТЕЗ</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Glazunova</surname><given-names>E. V</given-names></name><name xml:lang="ru"><surname>Глазунова</surname><given-names>Е. В</given-names></name></name-alternatives><email>email@example.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Kurnosov</surname><given-names>A. S</given-names></name><name xml:lang="ru"><surname>Курносов</surname><given-names>А. С</given-names></name></name-alternatives><email>email@example.com</email><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Molodtsova</surname><given-names>P. A</given-names></name><name xml:lang="ru"><surname>Молодцова</surname><given-names>П. А</given-names></name></name-alternatives><email>email@example.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Moskalenko</surname><given-names>A. M</given-names></name><name xml:lang="ru"><surname>Москаленко</surname><given-names>А. М</given-names></name></name-alternatives><email>email@example.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Makarov</surname><given-names>V. V</given-names></name><name xml:lang="ru"><surname>Макаров</surname><given-names>В. В</given-names></name></name-alternatives><email>email@example.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Zlobovskaya</surname><given-names>O. A</given-names></name><name xml:lang="ru"><surname>Злобовская</surname><given-names>О. А</given-names></name></name-alternatives><email>ozlobovskaya@cspfmba.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Center for Strategic Planning and Management of Biomedical Health Risks, Federal Medical and Biological Agency</institution></aff><aff><institution xml:lang="ru">Центр стратегического планирования и управления медико-биологическими рисками здоровью Федерального медико-биологического агентства</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">Emanuel Institute of Biochemical Physics, Russian Academy of Sciences</institution></aff><aff><institution xml:lang="ru">Институт биохимической физики им. Н.М. Эммануэля Российской академии наук</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2025-12-25" publication-format="electronic"><day>25</day><month>12</month><year>2025</year></pub-date><volume>59</volume><issue>6</issue><issue-title xml:lang="en">VOL 59, NO6 (2025)</issue-title><issue-title xml:lang="ru">ТОМ 59, №6 (2025)</issue-title><fpage>891</fpage><lpage>908</lpage><history><date date-type="received" iso-8601-date="2025-12-27"><day>27</day><month>12</month><year>2025</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2025, Russian Academy of Sciences</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2025, Российская академия наук</copyright-statement><copyright-year>2025</copyright-year><copyright-holder xml:lang="en">Russian Academy of Sciences</copyright-holder><copyright-holder xml:lang="ru">Российская академия наук</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/" start_date="2026-12-25"/></permissions><self-uri xlink:href="https://vietnamjournal.ru/0026-8984/article/view/699674">https://vietnamjournal.ru/0026-8984/article/view/699674</self-uri><abstract xml:lang="en"><p>Colorectal cancer remains one of the leading causes of cancer-related mortality, highlighting the importance of optimizing approaches for its early diagnosis and therapy. One promising area in this field is the study of the gut microbiome’s role in the initiation and progression of colorectal cancer. This review examines three main theories explaining the microbiota’s contribution to carcinogenesis: the "Alpha-bug" theory, the "Keystone pathogen" hypothesis, and the "Driver–Passenger" model. The review analyzes data on the mechanisms of microbiota interaction with tumor cells, including inflammation induction, genotoxicity, and disruption of the intestinal barrier function. The review also presents research findings demonstrating that some microorganisms, previously considered markers of late-stage disease, may possess pro-oncogenic properties, refining existing carcinogenesis models. The presented data suggest that the microbiota and its dysbiotic alterations could be considered potential targets for colorectal cancer diagnosis and therapy.</p></abstract><trans-abstract xml:lang="ru"><p>Колоректальный рак остается одной из ведущих причин смертности от онкологических заболеваний, что обусловливает важность оптимизации подходов к его ранней диагностике и терапии. Одним из перспективных направлений в этой области является изучение роли кишечного микробиома в инициации и развитии колоректального рака. В обзоре рассмотрены три основные гипотезы, объясняющие вклад микробиоты в канцерогенез: модели "Alpha-bug", "Keystone pathogen" и "Driver–Passenger". Проанализированы данные о механизмах взаимодействия микробиоты с опухолевыми клетками, включая индукцию воспаления, генотоксичность и нарушение барьерной функции кишечника. Обсуждаются результаты, показавшие, что некоторые микроорганизмы, ранее считавшиеся маркерами поздних стадий рака, могут обладать проэнкогенными свойствами, что уточняет существующие модели канцерогенеза. Представленные данные позволяют рассматривать микробиоту и ее дисбиотические нарушения как потенциальную мишень для диагностики и терапии колоректального рака.</p></trans-abstract><kwd-group xml:lang="en"><kwd>colorectal cancer</kwd><kwd>diagnostics</kwd><kwd>biomarkers</kwd><kwd>carcinogenesis hypotheses</kwd><kwd>human gut microbiota</kwd><kwd>dysbiosis</kwd><kwd>microbiome</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>колоректальный рак</kwd><kwd>диагностика</kwd><kwd>биомаркеры</kwd><kwd>гипотезы канцерогенеза</kwd><kwd>микробиота кишечника человека</kwd><kwd>дисбиоз</kwd><kwd>микробиом</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Bray F., Laversanne M., Sung H., Ferlay J., Siegel R.L., Soerjomataram I., Jemal A. (2024) Global cancer statistics 2022: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. <italic>CA Cancer J. 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