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钠转运体抑制导致显著衰老。

Striking senescence with sodium transporter inhibition.

作者信息

Schock Bettina, O'Reilly Steven

机构信息

Wellcome-Woolfson Institute for Experimental Medicine, Queens University Belfast 97 Lisburn Road, Belfast, UK.

Biosciences, Durham University, South Road, Durham, UK.

出版信息

Trends Mol Med. 2024 Nov;30(11):1004-1006. doi: 10.1016/j.molmed.2024.07.002. Epub 2024 Jul 14.

Abstract

Senescence is associated with multiple morbidities and therapeutic targeting of these cells is a key aim. In a recent study, Katsuumi et al. found that targeting sodium-glucose co-transporter 2 (SGLT2) promoted immune clearance of senescent cells via programmed cell death-1 ligand (PD-L1) suppression, thus promoting immunosurveillance. This could have profound implications for many age-related diseases, including cancer and frailty.

摘要

细胞衰老与多种疾病相关,针对这些细胞进行治疗是一个关键目标。在最近的一项研究中,胜海等人发现,靶向钠-葡萄糖协同转运蛋白2(SGLT2)可通过抑制程序性细胞死亡蛋白1配体(PD-L1)促进衰老细胞的免疫清除,从而增强免疫监视。这可能对包括癌症和虚弱在内的许多与年龄相关的疾病产生深远影响。

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Striking senescence with sodium transporter inhibition.钠转运体抑制导致显著衰老。
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