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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="other" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Reviews on Clinical Pharmacology and Drug Therapy</journal-id><journal-title-group><journal-title xml:lang="en">Reviews on Clinical Pharmacology and Drug Therapy</journal-title><trans-title-group xml:lang="ru"><trans-title>Обзоры по клинической фармакологии и лекарственной терапии</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1683-4100</issn><issn publication-format="electronic">2542-1875</issn><publisher><publisher-name xml:lang="en">Eco-Vector</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">691330</article-id><article-id pub-id-type="doi">10.17816/RCF691330</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>Научные обзоры</subject></subj-group><subj-group subj-group-type="article-type"><subject>Unknown</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Features of metabolic cell death: ferroptosis, cuproptosis, disulfideptosis, lysozinctosis, alkaliptosis in cancer. Pharmacological basis of drug therapy</article-title><trans-title-group xml:lang="ru"><trans-title>Особенности метаболической гибели клеток: ферроптоза, купроптoза, дисульфидптоза, лизоцинктоза, алкалиптоза при раке. Фармакологический базис лекарственной терапии</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-3908-143X</contrib-id><name-alternatives><name xml:lang="en"><surname>Vashchenko</surname><given-names>Vladimir Ivanovich</given-names></name><name xml:lang="ru"><surname>Ващенко</surname><given-names>Владимир Иванович</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Senior Researcher, Dept of Blood and Tissues</p></bio><bio xml:lang="ru"><p>старший научный сотрудник Центра крови и тканей</p></bio><email>vladimir-vaschenko@yandex.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-1464-1127</contrib-id><name-alternatives><name xml:lang="en"><surname>Shabanov</surname><given-names>Petr</given-names></name><name xml:lang="ru"><surname>Шабанов</surname><given-names>Петр Дмитриевич</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Professor, Dr. Med. Sci. (Pharmacology), Head of the Department</p></bio><bio xml:lang="ru"><p>доктор медицинских наук, профессор, заведующий отделом</p></bio><email>pdshabanov@mail.ru</email><xref ref-type="aff" rid="aff2"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Kirov Military Medical Academy</institution></aff><aff><institution xml:lang="ru">ФГБВОУ ВО "Военно-медицинская академия им. С.М. Кирова" МО РФ</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">Institute of Experimental Medicine, St. Petersburg</institution></aff><aff><institution xml:lang="ru">Институт экспериментальной медицины, Санкт-Петербург</institution></aff></aff-alternatives><pub-date date-type="preprint" iso-8601-date="2026-02-07" publication-format="electronic"><day>07</day><month>02</month><year>2026</year></pub-date><volume>1</volume><issue>1</issue><issue-title xml:lang="ru"/><history><date date-type="received" iso-8601-date="2025-09-25"><day>25</day><month>09</month><year>2025</year></date><date date-type="accepted" iso-8601-date="2026-02-07"><day>07</day><month>02</month><year>2026</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; , Eco-Vector</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; , Эко-Вектор</copyright-statement><copyright-holder xml:lang="en">Eco-Vector</copyright-holder><copyright-holder xml:lang="ru">Эко-Вектор</copyright-holder><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://eco-vector.com/for_authors.php#07</ali:license_ref></license></permissions><self-uri xlink:href="https://journals.eco-vector.com/RCF/article/view/691330">https://journals.eco-vector.com/RCF/article/view/691330</self-uri><abstract xml:lang="en"><p>Fastness of tumoral cells to destruction in comparison with a healthy tissue represents a distinctive sign of cancer cells (effect of Varburg). Recent studies have identified metabolic cell death as unique forms of regulated cell death resulting from an imbalance in the cellular metabolism. Cell death is critical for the development and homeostasis of almost all multicellular organisms. Moreover, its dysregulation leads to diverse disease states. Historically, apoptosis was thought to be the major regulated cell death pathway, whereas necrosis was considered to be an unregulated form of cell death. However, research in recent decades has uncovered several forms of regulated necrosis that are implicated in degenerative diseases, inflammatory conditions and cancer. The growing insight into these regulated, non-apoptotic cell death pathways has opened new avenues for therapeutic targeting. Here, we describe the regulatory pathways of necroptosis, pyroptosis, parthanatos, ferroptosis, cuproptosis, lysozincrosis and disulfidptosis. This review discusses the mechanisms of metabolic cell death and explores their potential in cancer therapy. review underscores the complexity of the metabolic cell death pathways and offers insights into innovative therapeutic avenues for cancer treatment.</p> <p>In the article, we discuss small-molecule inhibitors of the pathways and prospects for future drug discovery. Together, the complex mechanisms governing these pathways offer strategies to develop therapeutics that control non-apoptotic cell death.</p></abstract><trans-abstract xml:lang="ru"><p>Устойчивость опухолевых клеток к гибели в сравнении со здоровой тканью представляет собой отличительный признак раковых клеток (эффект Варбурга). Недавние исследования идентифицировали метаболический некроз клеток как уникальные формы отрегулированного некроза клеток, следующего из дисбалланса в клеточном метаболизме. Некроз клеток важен для развития и гомеостаза почти всех многоклеточных организмов. Кроме того, дисрегуляция некроза приводит к разнообразным болезненным состояниям. Исторически, апоптоз, как полагали, был запрограммированным путем разрушения клеток главного предмета специализации, тогда как некроз, по определению, являлся нерегулируемой формой гибели клеток. Однако исследования, выполненные в последние десятилетия, раскрыли несколько важных форм регулируемой гибели клеток, которые являются частью механизма дегенеративных заболеваний, воспалительных заболеваний и рака. Растущее понимание этих регулируемых, неапоптозных путей гибели клеток открывают новые перспективы для терапевтических стратегий. Здесь, мы описываем регулирующими путями гибели клеток: некроптозом, феррроптозом, купроптозом, аутофагией, лизоцинктозом и дисульфидптoзом. В статье обсуждаются механизмы метаболической гибели клеток и исследует их потенциал в терапии рака. Подчеркивается сложность метаболических путей гибели клеток и предлагаются новаторские идеи проникновения в суть терапевтических перспектив для лечения рака.</p> <p>В статье обсуждаются ингибиторы малых молекул регулирующих путей и перспектив будущего изобретения лекарства против рака. Вместе взятые сложные механизмы, управляющие этими проводящими путями, предлагают стратегии по разработке терапии, которые включают разные формы неапоптозной гибели клеток.</p></trans-abstract><kwd-group xml:lang="en"><kwd>Ferroptosis, Cuproptosis, Disulfidptosis, Lisolzinсrosis, Alcaliptosis, Regulated cell death</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>регулируемая клеточная гибель, ферроптоз, купроптоз, дисульфидптоз, лизоцинктоз, алкалиптоз</kwd></kwd-group><funding-group><funding-statement xml:lang="en">Kirov Military Medical Academy</funding-statement><funding-statement xml:lang="ru">Военно-медицинская академия им. С.М. 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