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Ferroptosis, a new form of cell death: mechanisms, biology and role in gynecological malignant tumor. | LitMetric

AI Article Synopsis

  • Ferroptosis is an iron-related form of regulated cell death characterized by an accumulation of lipid peroxides in cell membranes, distinct from apoptosis and other cell death types.
  • It is linked to various diseases, including neurodegenerative disorders, chronic cardiovascular issues, respiratory diseases, and tumors, but research on its role in gynecological diseases is limited.
  • The article reviews existing studies on ferroptosis, examines its mechanisms, and highlights the need for further research to understand its implications for treating gynecological tumors and other related conditions.

Article Abstract

Ferroptosis, a term coined by Dixon et al. in 2012, refers to an iron-dependent form of regulated cell death driven by an overload of lipid peroxides on cellular membranes. It is morphologically and mechanistically distinct from apoptosis and other types of regulated cell death. Many studies have confirmed that ferroptosis is involved in the occurrence and development of many diseases, such as neurodegenerative diseases, chronic cardiovascular diseases, respiratory diseases and even tumors. While in the systemic diseases of obstetrics and gynecology, the related researches are still limited. In this article, we retrieved PubMed and WEB OF SCI databases for articles and reviews published before May 6, 2022, using "ferroptosis, ferroptosis regulator, gynecological tumors" as keywords, and comprehensively reviewed on their basis. Here, we systematically summarize the studies on the mechanism and characteristics of ferroptosis, investigate the role of ferroptosis in clinical systemic diseases of obstetrics and gynecology, evaluate the research status, unsolved problems and further research directions of ferroptosis, so as to let people learn more about ferroptosis and establish a research foundation for the exploration of the treatment strategies for ferroptosis-mediated diseases.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10408495PMC

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