Ferroptosis as a Novel Therapeutic Target for Diabetes and Its Complications
The global diabetes epidemic and its complications are increasing, thereby posing a major threat to public health. A comprehensive understanding of diabetes mellitus (DM) and its complications is necessary for the development of effective treatments. Ferroptosis is a newly identified form of program...
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Published in | Frontiers in endocrinology (Lausanne) Vol. 13; p. 853822 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Media S.A
29.03.2022
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Subjects | |
Online Access | Get full text |
ISSN | 1664-2392 1664-2392 |
DOI | 10.3389/fendo.2022.853822 |
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Summary: | The global diabetes epidemic and its complications are increasing, thereby posing a major threat to public health. A comprehensive understanding of diabetes mellitus (DM) and its complications is necessary for the development of effective treatments. Ferroptosis is a newly identified form of programmed cell death caused by the production of reactive oxygen species and an imbalance in iron homeostasis. Increasing evidence suggests that ferroptosis plays a pivotal role in the pathogenesis of diabetes and diabetes-related complications. In this review, we summarize the potential impact and regulatory mechanisms of ferroptosis on diabetes and its complications, as well as inhibitors of ferroptosis in diabetes and diabetic complications. Therefore, understanding the regulatory mechanisms of ferroptosis and developing drugs or agents that target ferroptosis may provide new treatment strategies for patients with diabetes. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 ObjectType-Review-3 content type line 23 This article was submitted to Diabetes: Molecular Mechanisms, a section of the journal Frontiers in Endocrinology Edited by: Ana Stancic, University of Belgrade, Serbia Reviewed by: Isha Sharma, Northwestern University, United States; Shuangqing Liu, Fourth Medical Center of PLA General Hospital, China; Ping Yao, Huazhong University of Science and Technology, China |
ISSN: | 1664-2392 1664-2392 |
DOI: | 10.3389/fendo.2022.853822 |