PMID- 36060972 OWN - NLM STAT- MEDLINE DCOM- 20220908 LR - 20220914 IS - 1664-2392 (Print) IS - 1664-2392 (Electronic) IS - 1664-2392 (Linking) VI - 13 DP - 2022 TI - Research progress on the mechanism of beta-cell apoptosis in type 2 diabetes mellitus. PG - 976465 LID - 10.3389/fendo.2022.976465 [doi] LID - 976465 AB - Type 2 diabetes mellitus(T2DM) is regarded as one of the most severe chronic metabolic diseases worldwide, which poses a great threat to human safety and health. The main feature of T2DM is the deterioration of pancreatic beta-cell function. More and more studies have shown that the decline of pancreatic beta-cell function in T2DM can be attributable to beta-cell apoptosis, but the exact mechanisms of beta-cell apoptosis in T2DM are not yet fully clarified. Therefore, in this review, we will focus on the current status and progress of research on the mechanism of pancreatic beta-cell apoptosis in T2DM, to provide new ideas for T2DM treatment strategies. CI - Copyright (c) 2022 You, Zheng, Chen and Huang. FAU - You, SuFang AU - You S AD - The Second Clinical Medical College of Fujian Medical University, Quanzhou, China. AD - Department of Endocrinology, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, China. FAU - Zheng, JingYi AU - Zheng J AD - Department of Endocrinology, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, China. FAU - Chen, YuPing AU - Chen Y AD - Department of Endocrinology, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, China. FAU - Huang, HuiBin AU - Huang H AD - Department of Endocrinology, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, China. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PT - Review DEP - 20220818 PL - Switzerland TA - Front Endocrinol (Lausanne) JT - Frontiers in endocrinology JID - 101555782 SB - IM MH - Apoptosis MH - *Diabetes Mellitus, Type 2/metabolism MH - Humans MH - *Insulin-Secreting Cells/metabolism MH - Pancreas/metabolism PMC - PMC9434279 OTO - NOTNLM OT - apoptosis OT - beta-cell OT - exosomes OT - glucolipotoxicity OT - molecular mechanisms OT - non-coding RNAs OT - type 2 diabetes COIS- The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. EDAT- 2022/09/06 06:00 MHDA- 2022/09/09 06:00 PMCR- 2022/01/01 CRDT- 2022/09/05 04:01 PHST- 2022/06/23 00:00 [received] PHST- 2022/08/01 00:00 [accepted] PHST- 2022/09/05 04:01 [entrez] PHST- 2022/09/06 06:00 [pubmed] PHST- 2022/09/09 06:00 [medline] PHST- 2022/01/01 00:00 [pmc-release] AID - 10.3389/fendo.2022.976465 [doi] PST - epublish SO - Front Endocrinol (Lausanne). 2022 Aug 18;13:976465. doi: 10.3389/fendo.2022.976465. eCollection 2022.