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Disulfidptosis, A Novel Cell Death Pathway: Molecular Landscape and Therapeutic Implications.
Gu, Qiuyang; An, Yumei; Xu, Mingyuan; Huang, Xinqi; Chen, Xueshi; Li, Xianzhe; Shan, Haiyan; Zhang, Mingyang.
Afiliación
  • Gu Q; Institute of Forensic Sciences, Suzhou Medical College, Soochow University, Suzhou, China.
  • An Y; Institute of Forensic Sciences, Suzhou Medical College, Soochow University, Suzhou, China.
  • Xu M; Institute of Forensic Sciences, Suzhou Medical College, Soochow University, Suzhou, China.
  • Huang X; Institute of Forensic Sciences, Suzhou Medical College, Soochow University, Suzhou, China.
  • Chen X; Institute of Forensic Sciences, Suzhou Medical College, Soochow University, Suzhou, China.
  • Li X; Institute of Forensic Sciences, Suzhou Medical College, Soochow University, Suzhou, China.
  • Shan H; Department of Obstetrics and Gynecology, The Affiliated Suzhou Hospital of Nanjing Medical University, Suzhou, China.
  • Zhang M; Institute of Forensic Sciences, Suzhou Medical College, Soochow University, Suzhou, China.
Aging Dis ; 2024 May 08.
Article en En | MEDLINE | ID: mdl-38739940
ABSTRACT
Programmed cell death is pivotal for several physiological processes, including immune defense. Further, it has been implicated in the pathogenesis of developmental disorders and the onset of numerous diseases. Multiple modes of programmed cell death, including apoptosis, pyroptosis, necroptosis, and ferroptosis, have been identified, each with their own unique characteristics and biological implications. In February 2023, Liu Xiaoguang and his team discovered "disulfidptosis," a novel pathway of programmed cell death. Their findings demonstrated that disulfidptosis is triggered in glucose-starved cells exhibiting high expression of a protein called SLC7A11. Furthermore, disulfidptosis is marked by a drastic imbalance in the NADPH/NADP+ ratio and the abnormal accumulation of disulfides like cystine. These changes ultimately lead to the destabilization of the F-actin network, causing cell death. Given that high SLC7A11 expression is a key feature of certain cancers, these findings indicate that disulfidptosis could serve as the basis of innovative anti-cancer therapies. Hence, this review delves into the discovery of disulfidptosis, its underlying molecular mechanisms and metabolic regulation, and its prospective applications in disease treatment.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Aging Dis Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Aging Dis Año: 2024 Tipo del documento: Article País de afiliación: China
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