4.6 Review

Molecular mechanism of ferroptosis and its role in the occurrence and treatment of diabetes

Journal

FRONTIERS IN GENETICS
Volume 13, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fgene.2022.1018829

Keywords

ferroptosis; diabetes; ROS; GPX4; lipid peroxide; ferroptosis inhibitor

Funding

  1. National Natural Science Foundation of China [81802504, 81872207]
  2. Sichuan Science and Technology Bureau [2019YFS0439, 2020JDJQ0067, 2020JDRC0118, 2021YJ0564, 2022YFH0005]
  3. Science and Technology Innovation Project of Chengdu, China [2021-YF05-00225-SN]
  4. Sichuan Medical Association [Q19037]

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This article reviews the molecular mechanism of ferroptosis in the development of diabetes mellitus and its complications, highlighting emerging questions in this particular research area. It provides novel insights in the treatment of diabetes from the perspective of ferroptosis.
Ferroptosis is an iron-dependent programmed cell death, which is different from apoptosis, necrosis, and autophagy. Specifically, under the action of divalent iron or ester oxygenase, unsaturated fatty acids that are highly expressed on the cell membrane are catalyzed to produce lipid peroxidation, which induces cell death. In addition, the expression of the antioxidant system [glutathione (GSH) and glutathione peroxidase 4 (GPX4)] is decreased. Ferroptosis plays an important role in the development of diabetes mellitus and its complications. In this article, we review the molecular mechanism of ferroptosis in the development of diabetes mellitus and its complications. We also summarize the emerging questions in this particular area of research, some of which remain unanswered. Overall, this is a comprehensive review focusing on ferroptosis-mediated diabetes and providing novel insights in the treatment of diabetes from the perspective of ferroptosis.

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