Regulation of Cellular Senescence in Type 2 Diabetes Mellitus: From Mechanisms to Clinical Applications

被引:17
|
作者
Iwasaki, Kanako [1 ,2 ]
Abarca, Cristian [1 ]
Aguayo-Mazzucato, Cristina [1 ,3 ]
机构
[1] Harvard Med Sch, Joslin Diabet Ctr, Boston, MA USA
[2] Kitano Hosp, Tazuke Kofukai Med Res Inst, Osaka, Japan
[3] Harvard Med Sch, Joslin Diabet Ctr, One Joslin Pl, Boston, MA 02215 USA
基金
美国国家卫生研究院;
关键词
Aging; Diabetes mellitus; type; 2; Insulin-secreting cells; Senotherapeutics; TUBULAR EPITHELIAL-CELLS; SECRETORY PHENOTYPE; PREMATURE SENESCENCE; BCL-2; FAMILY; LIFE-SPAN; CURCUMIN; IMPACT; MITOCHONDRIAL; PROGRESSION; FIBROBLASTS;
D O I
10.4093/dmj.2022.0416
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cellular senescence is accelerated by hyperglycemia through multiple pathways. Therefore, senescence is an important cellular mechanism to consider in the pathophysiology of type 2 diabetes mellitus (T2DM) and an additional therapeutic target. The use of drugs that remove senescent cells has led to improvements in blood glucose levels and diabetic complications in animal studies. Although the removal of senescent cells is a promising approach for the treatment of T2DM, two main challenges limit its clinical application: the molecular basis of cellular senescence in each organ is yet to be understood, and the specific effect of removing senescent cells in each organ has to be determined. This review aims to discuss future applications of targeting senescence as a therapeutic option in T2DM and elucidate the characteristics of cellular senescence and senescence-associated secretory pheno-type in the tissues important for regulating glucose levels: pancreas, liver, adipocytes, and skeletal muscle.
引用
收藏
页码:441 / 453
页数:13
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