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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">Acta Naturae</journal-id><journal-title-group><journal-title xml:lang="en">Acta Naturae</journal-title><trans-title-group xml:lang="ru"><trans-title>Acta Naturae</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2075-8251</issn><publisher><publisher-name xml:lang="en">Acta Naturae Ltd</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">27547</article-id><article-id pub-id-type="doi">10.32607/actanaturae.27547</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Reviews</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><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">Pro-inflammatory cytokines, ferroptosis, and cancer</article-title><trans-title-group xml:lang="ru"><trans-title>Провоспалительные цитокины в ферроптозе при раке</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Vartanian</surname><given-names>A. A.</given-names></name><name xml:lang="ru"><surname>Вартанян</surname><given-names>A. A.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>zhivotov57@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Kosorukov</surname><given-names>V. S.</given-names></name><name xml:lang="ru"><surname>Косоруков</surname><given-names>B. C.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>zhivotov57@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">N.N. Blokhin National Medical Research Center of Oncology of the Ministry of Health of Russia</institution></aff><aff><institution xml:lang="ru">Национальный медицинский исследовательский центр онкологии им. Н.Н. Блохина Минздрава России</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2025-04-22" publication-format="electronic"><day>22</day><month>04</month><year>2025</year></pub-date><volume>17</volume><issue>1</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>4</fpage><lpage>10</lpage><history><date date-type="received" iso-8601-date="2024-10-24"><day>24</day><month>10</month><year>2024</year></date><date date-type="accepted" iso-8601-date="2024-11-08"><day>08</day><month>11</month><year>2024</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2025, Vartanian A.A., Kosorukov V.S.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2025, Вартанян A.A., Косоруков B.C.</copyright-statement><copyright-year>2025</copyright-year><copyright-holder xml:lang="en">Vartanian A.A., Kosorukov V.S.</copyright-holder><copyright-holder xml:lang="ru">Вартанян A.A., Косоруков B.C.</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://actanaturae.ru/2075-8251/article/view/27547">https://actanaturae.ru/2075-8251/article/view/27547</self-uri><abstract xml:lang="en"><p>Ferroptosis, iron-dependent regulated cell death, is induced by the polyunsaturated fatty acid peroxidation of membrane phospholipids and is controlled by glutathione peroxidase 4. In recent years, convincing evidence has emerged, demonstrating a close relationship between chemo-, radio-, immuno-, and targeted therapy resistance and ferroptosis resistance. In this review, we discuss the basic principles of ferroptosis in cancer. Considerable attention is paid to the formation of an immunosuppressive tumor microenvironment. The main focus is centered on the involvement of the excessive, chronic production of pro-inflammatory cytokines in ferroptosis resistance development in tumors.</p></abstract><trans-abstract xml:lang="ru"><p>Ферроптоз, или железозависимая регулируемая гибель клетки, индуцируется перекисным окислением полиненасыщенных жирных кислот фосфолипидов мембран и находится под контролем глутатионпероксидазы-4. В последние годы получены убедительные данные, свидетельствующие о том, что резистентность к химио-, радио-, иммуно- и таргетной терапии опухоли тесно связана с резистентностью к ферроптозу. В обзоре обсуждаются молекулярные характеристики ферроптоза при раке. Значительное внимание уделено образованию иммуносупрессивного пространства на территории опухоли. Основной акцент сделан на вовлечение хронической избыточной продукции провоспалительных цитокинов в становлении резистентности к ферроптозу.</p></trans-abstract><kwd-group xml:lang="en"><kwd>ferroptosis</kwd><kwd>intratumoral immunosuppression</kwd><kwd>pro-inflamatory cytokines</kwd><kwd>cancer</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>рак</kwd><kwd>ферроптоз</kwd><kwd>внутриопухолевая иммуносупрессия</kwd><kwd>провоспалительные цитокины</kwd></kwd-group><funding-group><award-group><funding-source><institution-wrap><institution xml:lang="en">Ministry of Health of the Russian Federation</institution></institution-wrap><institution-wrap><institution xml:lang="ru">Министерство здравоохранения Российской Федерации</institution></institution-wrap></funding-source><award-id>056-00065-23 ПР</award-id></award-group></funding-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>de Visser K.E., Joyce J.A. // Cancer Cell. 2023. V. 41. № 3. 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