Role of ferroptosis inhibitors in the management of diabetes
Ferroptosis, the iron‐dependent, lipid peroxide‐mediated cell death, has garnered attention due to its critical involvement in crucial physiological and pathological cellular processes. Indeed, several studies have attributed its role in developing a range of disorders, including diabetes. As accumu...
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Veröffentlicht in: | BioFactors (Oxford) 2023-03, Vol.49 (2), p.270-296 |
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description | Ferroptosis, the iron‐dependent, lipid peroxide‐mediated cell death, has garnered attention due to its critical involvement in crucial physiological and pathological cellular processes. Indeed, several studies have attributed its role in developing a range of disorders, including diabetes. As accumulating evidence further the understanding of ferroptotic mechanisms, the impact this specialized mode of cell death has on diabetic pathogenesis is still unclear. Several in vivo and in vitro studies have highlighted the association of ferroptosis with beta‐cell death and insulin resistance, supported by observations of marked alterations in ferroptotic markers in experimental diabetes models. The constant improvement in understanding ferroptosis in diabetes has demonstrated it as a potential therapeutic target in diabetic management. In this regard, ferroptosis inhibitors promise to rescue pancreatic beta‐cell function and alleviate diabetes and its complications. This review article elucidates the key ferroptotic pathways that mediate beta‐cell death in diabetes, and its complications. In particular, we share our insight into the cross talk between ferroptosis and other hallmark pathogenic mediators such as oxidative and endoplasmic reticulum stress regulators relevant to diabetes progression. Further, we extensively summarize the recent developments on the role of ferroptosis inhibitors and their therapeutic action in alleviating diabetes and its complications. |
doi_str_mv | 10.1002/biof.1920 |
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Indeed, several studies have attributed its role in developing a range of disorders, including diabetes. As accumulating evidence further the understanding of ferroptotic mechanisms, the impact this specialized mode of cell death has on diabetic pathogenesis is still unclear. Several in vivo and in vitro studies have highlighted the association of ferroptosis with beta‐cell death and insulin resistance, supported by observations of marked alterations in ferroptotic markers in experimental diabetes models. The constant improvement in understanding ferroptosis in diabetes has demonstrated it as a potential therapeutic target in diabetic management. In this regard, ferroptosis inhibitors promise to rescue pancreatic beta‐cell function and alleviate diabetes and its complications. This review article elucidates the key ferroptotic pathways that mediate beta‐cell death in diabetes, and its complications. In particular, we share our insight into the cross talk between ferroptosis and other hallmark pathogenic mediators such as oxidative and endoplasmic reticulum stress regulators relevant to diabetes progression. 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In particular, we share our insight into the cross talk between ferroptosis and other hallmark pathogenic mediators such as oxidative and endoplasmic reticulum stress regulators relevant to diabetes progression. Further, we extensively summarize the recent developments on the role of ferroptosis inhibitors and their therapeutic action in alleviating diabetes and its complications.</description><subject>Cell Death</subject><subject>diabetes</subject><subject>Diabetes Mellitus - drug therapy</subject><subject>Diabetes Mellitus - genetics</subject><subject>ferroptosis</subject><subject>Ferroptosis - genetics</subject><subject>ferroptosis inhibitors</subject><subject>GPX4</subject><subject>iron</subject><subject>Iron - metabolism</subject><subject>Lipid Peroxidation</subject><subject>Lipid Peroxides - metabolism</subject><issn>0951-6433</issn><issn>1872-8081</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kEtLw0AURgdRbH0s_AOSpS7Szjsz4EaL1UKhILoeJskdO5JkaiZF-u9NbHXn6t7F4cB3ELoieEIwptPcBzchmuIjNCYqo6nCihyjMdaCpJIzNkJnMX5gTBjm6hSNmORScc7G6O4lVJAElzho27DpQvQx8c3a574L7fAm3RqS2jb2HWpouoEtvc2hg3iBTpytIlwe7jl6mz--zp7T5eppMbtfpgWjAqfWZTmXeVkIQrQqSOmcBiqcJJQIInguFICUEhi1mLKMa8aUldQ6XRY6k-wc3ey9mzZ8biF2pvaxgKqyDYRtNDTjGe6XCd2jt3u0aEOMLTizaX1t250h2AyxzBDLDLF69vqg3eY1lH_kb50emO6BL1_B7n-TeVis5j_Kb5E8crk</recordid><startdate>202303</startdate><enddate>202303</enddate><creator>Prasad M, Krishna</creator><creator>Mohandas, Sundhar</creator><creator>Kunka Mohanram, Ramkumar</creator><general>John Wiley & Sons, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-5450-902X</orcidid></search><sort><creationdate>202303</creationdate><title>Role of ferroptosis inhibitors in the management of diabetes</title><author>Prasad M, Krishna ; Mohandas, Sundhar ; Kunka Mohanram, Ramkumar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3250-af7b46bdc51198c1dff9e25f61215154b58ee666e32a023749338a62af9dc9763</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Cell Death</topic><topic>diabetes</topic><topic>Diabetes Mellitus - drug therapy</topic><topic>Diabetes Mellitus - genetics</topic><topic>ferroptosis</topic><topic>Ferroptosis - genetics</topic><topic>ferroptosis inhibitors</topic><topic>GPX4</topic><topic>iron</topic><topic>Iron - metabolism</topic><topic>Lipid Peroxidation</topic><topic>Lipid Peroxides - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Prasad M, Krishna</creatorcontrib><creatorcontrib>Mohandas, Sundhar</creatorcontrib><creatorcontrib>Kunka Mohanram, Ramkumar</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>BioFactors (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Prasad M, Krishna</au><au>Mohandas, Sundhar</au><au>Kunka Mohanram, Ramkumar</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Role of ferroptosis inhibitors in the management of diabetes</atitle><jtitle>BioFactors (Oxford)</jtitle><addtitle>Biofactors</addtitle><date>2023-03</date><risdate>2023</risdate><volume>49</volume><issue>2</issue><spage>270</spage><epage>296</epage><pages>270-296</pages><issn>0951-6433</issn><eissn>1872-8081</eissn><abstract>Ferroptosis, the iron‐dependent, lipid peroxide‐mediated cell death, has garnered attention due to its critical involvement in crucial physiological and pathological cellular processes. 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subjects | Cell Death diabetes Diabetes Mellitus - drug therapy Diabetes Mellitus - genetics ferroptosis Ferroptosis - genetics ferroptosis inhibitors GPX4 iron Iron - metabolism Lipid Peroxidation Lipid Peroxides - metabolism |
title | Role of ferroptosis inhibitors in the management of diabetes |
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