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Inhibition of FSP1: A new strategy for the treatment of tumors (Review).
Dai, Qiangfang; Wei, Xiaoli; Zhao, Jumei; Zhang, Die; Luo, Yidan; Yang, Yue; Xiang, Yang; Liu, Xiaolong.
Afiliación
  • Dai Q; School of Medicine, Yan'an University, Yan'an, Shaanxi 716000, P.R. China.
  • Wei X; School of Medicine, Yan'an University, Yan'an, Shaanxi 716000, P.R. China.
  • Zhao J; School of Medicine, Yan'an University, Yan'an, Shaanxi 716000, P.R. China.
  • Zhang D; School of Medicine, Yan'an University, Yan'an, Shaanxi 716000, P.R. China.
  • Luo Y; School of Medicine, Yan'an University, Yan'an, Shaanxi 716000, P.R. China.
  • Yang Y; School of Medicine, Yan'an University, Yan'an, Shaanxi 716000, P.R. China.
  • Xiang Y; School of Medicine, Yan'an University, Yan'an, Shaanxi 716000, P.R. China.
  • Liu X; School of Medicine, Yan'an University, Yan'an, Shaanxi 716000, P.R. China.
Oncol Rep ; 52(2)2024 08.
Article en En | MEDLINE | ID: mdl-38940330
ABSTRACT
Ferroptosis, a regulated form of cell death, is intricately linked to iron­dependent lipid peroxidation. Recent evidence strongly supports the induction of ferroptosis as a promising strategy for treating cancers resistant to conventional therapies. A key player in ferroptosis regulation is ferroptosis suppressor protein 1 (FSP1), which promotes cancer cell resistance by promoting the production of the antioxidant form of coenzyme Q10. Of note, FSP1 confers resistance to ferroptosis independently of the glutathione (GSH) and glutathione peroxidase­4 pathway. Therefore, targeting FSP1 to weaken its inhibition of ferroptosis may be a viable strategy for treating refractory cancer. This review aims to clarify the molecular mechanisms underlying ferroptosis, the specific pathway by which FSP1 suppresses ferroptosis and the effect of FSP1 inhibitors on cancer cells.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Ferroptosis / Neoplasias Límite: Animals / Humans Idioma: En Revista: Oncol Rep Asunto de la revista: NEOPLASIAS Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Ferroptosis / Neoplasias Límite: Animals / Humans Idioma: En Revista: Oncol Rep Asunto de la revista: NEOPLASIAS Año: 2024 Tipo del documento: Article