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<article article-type="review-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">mes</journal-id><journal-title-group><journal-title xml:lang="ru">Экстремальная биомедицина</journal-title><trans-title-group xml:lang="en"><trans-title>Extreme Medicine</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2713-2757</issn><issn pub-type="epub">2713-2765</issn><publisher><publisher-name>Centre for Strategic Planning of the Federal Medical and Biological Agency</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.47183/mes.2025-250</article-id><article-id custom-type="elpub" pub-id-type="custom">mes-250</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>КЛИНИЧЕСКАЯ ФАРМАКОЛОГИЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CLINICAL PHARMACOLOGY</subject></subj-group></article-categories><title-group><article-title>Перспективы применения соединений растительного и грибного происхождения в противоопухолевой терапии</article-title><trans-title-group xml:lang="en"><trans-title>Application prospects of plant and fungal compounds in antitumor therapy</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-5086-5254</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Гасанова</surname><given-names>Т. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Gasanova</surname><given-names>T. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Гасанова Татьяна Владимировна, канд. биол. наук</p><p>Москва</p></bio><bio xml:lang="en"><p>Tatiana V. Gasanova, Cand. Sci. (Biol.)</p><p>Moscow</p></bio><email xlink:type="simple">tv.gasanova@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-0350-8021</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Иванов</surname><given-names>П. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Ivanov</surname><given-names>P. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Иванов Петр Алексеевич, канд. биол. наук</p><p>Москва</p></bio><bio xml:lang="en"><p>Peter A. Ivanov, Cand. Sci. (Biol.)</p><p>Moscow</p></bio><email xlink:type="simple">regaflight@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0005-5644-3438</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Репина</surname><given-names>М. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Repina</surname><given-names>M. N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Репина Мария Николаевна</p><p>Москва</p></bio><bio xml:lang="en"><p>Maria N. Repina</p><p>Moscow</p></bio><email xlink:type="simple">rep-masha@yandex.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru">Московский государственный университет им. М.В. Ломоносова<country>Россия</country></aff><aff xml:lang="en">Lomonosov Moscow State University<country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2025</year></pub-date><pub-date pub-type="epub"><day>08</day><month>09</month><year>2025</year></pub-date><volume>27</volume><issue>3</issue><fpage>309</fpage><lpage>319</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Гасанова Т.В., Иванов П.А., Репина М.Н., 2025</copyright-statement><copyright-year>2025</copyright-year><copyright-holder xml:lang="ru">Гасанова Т.В., Иванов П.А., Репина М.Н.</copyright-holder><copyright-holder xml:lang="en">Gasanova T.V., Ivanov P.A., Repina M.N.</copyright-holder><license 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.extrememedicine.ru/jour/article/view/250">https://www.extrememedicine.ru/jour/article/view/250</self-uri><abstract><sec><title>Введение</title><p>Введение. Ингибиторы растительного и грибного происхождения (ИРГП) представляют собой перспективное направление в противоопухолевой терапии, предлагая разнообразные механизмы действия, в большинстве случаев отличающиеся от традиционных химиотерапевтических препаратов. Как правило, ИРГП одновременно влияют на несколько метаболических путей, что снижает вероятность развития резистентности, оказывая комбинированный эффект на разные мишени в раковой клетке.</p></sec><sec><title>Цель</title><p>Цель. Изучить перспективные направления в создании новых противоопухолевых препаратов для последующего лечения, обобщить современные данные о механизмах действия ИРГП в контексте комплексного подхода к лечению злокачественных опухолей.</p></sec><sec><title>Обсуждение</title><p>Обсуждение. В настоящее время усиленно проводится поиск новых соединений с противоопухолевым потенциалом. ИРГП представляют собой перспективное направление в противоопухолевой терапии, предлагая разнообразные механизмы действия. Многие традиционные химиотерапевтические препараты также имеют растительное происхождение и обладают хорошей эффективностью, что подтверждает актуальность изучения данной тематики. Солидные опухоли обладают повышенной способностью к активной пролиферации и ангиогенезу, что объясняет неизменный интерес к активному поиску новых соединений растительного происхождения с антиангиогенными свойствами, наряду с исследованиями других ИРГП. Как правило, ИРГП одновременно влияют на несколько метаболических путей, что снижает вероятность развития резистентности, оказывая комбинированный эффект на разные мишени в раковой клетке.</p></sec><sec><title>Выводы</title><p>Выводы. В обзоре рассмотрены молекулярные механизмы действия ИРГП, включающие в себя подавление ангиогенеза и пролиферации раковых клеток, индукцию апоптоза, модуляцию клеточного цикла, а также прямой цитотоксический эффект путем стимуляции активности CD8+ Т-лимфоцитов, NK-клеток и макрофагов.</p></sec></abstract><trans-abstract xml:lang="en"><sec><title>Introduction</title><p>Introduction. Anticancer inhibitors of plant and fungal origin (IPFOs) represent a promising direction in antitumor therapy, offering a variety of mechanisms of action, in most cases different from conventional chemotherapeutic drugs. As a rule, IPFOs simultaneously affect several metabolic pathways, exerting a combined effect on different targets in the cancer cell and reducing the risk of drug resistance development.</p></sec><sec><title>Objective</title><p>Objective. To study promising directions in the development of new antitumor drugs, to generalize current data on the IPFO mechanism of action in the context of a combined approach to cancer treatment.</p></sec><sec><title>Discussion</title><p>Discussion. Compounds exhibiting antitumor activity are increasingly attracting the research attention. Due to their diverse mechanisms of action, anticancer IPFOs represent a promising direction in cancer treatment. A large number of conventional chemotherapy drugs, although being of plant origin, demonstrate high effectiveness, which confirms the relevance of searching for new anticancer IPFO compounds. Solid tumors exhibit a pronounced ability to both proliferate and induce angiogenesis, which justifies the current active search for new plant-derived compounds with antiangiogenic properties, along with other IPFOs. As a rule, anticancer IPFOs simultaneously affect several metabolic pathways, exerting a combined effect on different targets in the cancer cell and reducing the risk of drug resistance.</p></sec><sec><title>Conclusions</title><p>Conclusions. This review has examined the molecular mechanisms of IPFO action, including suppression of angiogenesis and cancer cells proliferation, apoptosis induction, cell cycle modulation, and direct cytotoxic effect by stimulating the activity of CD8+ T lymphocytes, NK cells, and macrophages.</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>противоопухолевая терапия</kwd><kwd>растительные и грибные ингибиторы опухолей</kwd><kwd>апоптоз</kwd><kwd>запрограммированная клеточная смерть</kwd><kwd>ангиогенез</kwd><kwd>аутофагия</kwd><kwd>ферроптоз</kwd><kwd>регуляция клеточного цикла</kwd></kwd-group><kwd-group xml:lang="en"><kwd>antitumor therapy</kwd><kwd>plant- and fungus-derived tumor inhibitors</kwd><kwd>apoptosis</kwd><kwd>programmed cell death</kwd><kwd>angiogenesis</kwd><kwd>autophagy</kwd><kwd>ferroptosis</kwd><kwd>cell cycle regulation</kwd></kwd-group><funding-group xml:lang="ru"><funding-statement>Исследование выполнено в рамках государственного задания № 121032500078-5 от 2021–2025 гг. ФГБУ «МГУ имени М.В. Ломоносова».</funding-statement></funding-group><funding-group xml:lang="en"><funding-statement>The research was carried out within the state assignment (theme No. 121032500078-5 of 2021–2025).</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">Амосова ЕН, Зуева ЕП, Разина ТГ, Крылова СГ. Лекарственные растения как средства дополнительной терапии для лечения опухолей. Бюллетень эксперимен­ тальной биологии и медицины. 2003;2:24–34. EDN: ULASLT</mixed-citation><mixed-citation xml:lang="en">Amosova EN, Zueva EP, Razina TK, Krylova SG. Medicinal plants as complementary therapies for the treatment of tumors. The Bulletin of experimental biology and medicine. 2003;2:24–34 (In Russ.). EDN: ULASLT</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Harvey AL. 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