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衰老起始阶段中的丝裂原活化蛋白激酶参与上皮-间充质转化过程。

MAPKs in the early steps of senescence implemEMTation.

作者信息

Anerillas Carlos, Altés Gisela, Gorospe Myriam

机构信息

Laboratory of Genetics and Genomics, National Institute on Aging Intramural Research Program, National Institutes of Health, Baltimore, MD, United States.

出版信息

Front Cell Dev Biol. 2023 Mar 16;11:1083401. doi: 10.3389/fcell.2023.1083401. eCollection 2023.

Abstract

Evidence is accumulating that the earliest stages of the DNA damage response can direct cells toward senescence instead of other cell fates. In particular, tightly regulated signaling through Mitogen-Activated Protein Kinases (MAPKs) in early senescence can lead to a sustained pro-survival program and suppress a pro-apoptotic program. Importantly, an epithelial-to-mesenchymal Transition (EMT)-like program appears essential for preventing apoptosis and favoring senescence following DNA damage. In this review, we discuss how MAPKs might influence EMT features to promote a senescent phenotype that increases cell survival at the detriment of tissue function.

摘要

越来越多的证据表明,DNA损伤反应的最早阶段可引导细胞走向衰老而非其他细胞命运。特别是,在早期衰老过程中,通过丝裂原活化蛋白激酶(MAPK)进行的严格调控信号传导可导致持续的促生存程序,并抑制促凋亡程序。重要的是,一种上皮-间质转化(EMT)样程序似乎对于防止DNA损伤后的细胞凋亡和促进衰老至关重要。在这篇综述中,我们讨论了MAPK如何影响EMT特征以促进衰老表型,这种表型以组织功能为代价增加细胞存活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79ec/10060890/ded5cbcfc55f/fcell-11-1083401-g001.jpg

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