Biomedicine & Pharmacotherapy, Год журнала: 2024, Номер 180, С. 117513 - 117513
Опубликована: Сен. 27, 2024
Язык: Английский
Biomedicine & Pharmacotherapy, Год журнала: 2024, Номер 180, С. 117513 - 117513
Опубликована: Сен. 27, 2024
Язык: Английский
Drug Design Development and Therapy, Год журнала: 2024, Номер Volume 18, С. 2485 - 2529
Опубликована: Июнь 1, 2024
Abstract: Ferroptosis, a unique form of programmed cell death, is initiated by an excess iron accumulation and lipid peroxidation-induced damage. There growing body evidence indicating that ferroptosis plays critical role in the advancement tumors. The increased metabolic activity higher levels tumor cells make them particularly vulnerable to ferroptosis. As result, targeted induction becoming increasingly promising approach for cancer treatment. This review offers overview regulatory mechanisms ferroptosis, delves into mechanism action traditional small molecule inducers their effects on various In addition, latest progress inducing using new means such as proteolysis-targeting chimeras (PROTACs), photodynamic therapy (PDT), sonodynamic (SDT) nanomaterials summarized. Finally, this discusses challenges opportunities development ferroptosis-inducing agents, focusing discovering targets, improving selectivity, reducing toxic side effects. Keywords: inducers, molecules, PROTACs, PDT, SDT,
Язык: Английский
Процитировано
10Free Radical Biology and Medicine, Год журнала: 2024, Номер 223, С. 224 - 236
Опубликована: Авг. 6, 2024
Язык: Английский
Процитировано
10International Immunopharmacology, Год журнала: 2025, Номер 148, С. 114048 - 114048
Опубликована: Янв. 18, 2025
Язык: Английский
Процитировано
1Journal of Colloid and Interface Science, Год журнала: 2025, Номер 686, С. 1074 - 1088
Опубликована: Фев. 6, 2025
Язык: Английский
Процитировано
1Chemico-Biological Interactions, Год журнала: 2025, Номер 412, С. 111459 - 111459
Опубликована: Март 5, 2025
Язык: Английский
Процитировано
1Life Sciences, Год журнала: 2025, Номер unknown, С. 123565 - 123565
Опубликована: Март 1, 2025
Язык: Английский
Процитировано
1ACS Nano, Год журнала: 2025, Номер unknown
Опубликована: Апрель 3, 2025
Disulfidptosis and ferroptosis are recently identified programmed cell deaths for tumor therapy, both of which highly depend on the intracellular cystine/cysteine transformation cystine transporter solute carrier family 7 member 11/glutathione/glutathione peroxidase 4 (SLC7A11/GSH/GPX4) antioxidant axis. However, disulfidptosis usually asynchronous due to opposite effect transport them. Herein, systematic glucose deprivation, by inhibiting upstream uptake promoting downstream consumption, is proposed synchronously evoke ferroptosis. As an example, Au nanodots Fe-apigenin (Ap) complexes coloaded FeOOH nanoshuttles (FeOOH@Fe-Ap@Au NSs) employed regulate SLC7A11/GSH/GPX4 axis performing disulfidptosis- ferroptosis-mediated therapy synchronously. In this scenario, exhibit oxidase-like activity when consuming massive glucose. Meanwhile, Ap can inhibit downregulating 1, depriving fundamentally. The systematical deprivation limits supplement NADPH suppresses axis, thus solving contradiction addition, efficient delivery exogenous iron ions FeOOH@Fe-Ap@Au NSs self-supplied H2O2 through nanodots-catalytic oxidation facilitate Fenton reaction therewith help amplify a result synchronous occurrence ferroptosis, good efficacy in ovarian cancer therapeutic model.
Язык: Английский
Процитировано
1Cellular Immunology, Год журнала: 2025, Номер unknown, С. 104948 - 104948
Опубликована: Апрель 1, 2025
Язык: Английский
Процитировано
1Phytomedicine, Год журнала: 2024, Номер 134, С. 155989 - 155989
Опубликована: Авг. 31, 2024
Язык: Английский
Процитировано
8Archives of Biochemistry and Biophysics, Год журнала: 2025, Номер 765, С. 110316 - 110316
Опубликована: Янв. 22, 2025
Язык: Английский
Процитировано
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