| Literature DB >> 32949791 |
Su Young Hwang1, Myeong Uk Kuk1, Jae Won Kim1, Yun Haeng Lee1, Young-Sam Lee2, Hyon E Choy3, Sang Chul Park4, Joon Tae Park5.
Abstract
Previously, we uncovered a novel mechanism in which senescence is controlled by mitochondrial functional recovery upon Ataxia-telangiectasia mutated (ATM) inhibition. However, it remains elusive how ATM controls signaling pathways to achieve restorative effect. In this study, we performed microarray and found that p53 pathway was differentially expressed upon ATM inhibition. We found that ATM inhibition yields senescence amelioration through p53-dependent manner. The restorative effect was also afforded by direct p53 inhibition. Furthermore, mitochondrial metabolic reprogramming via p53 inhibition was a prerequisite for senescence amelioration. Taken together, our data indicated that p53 pathway functions as potential target for ATM-mediated senescence amelioration.Entities:
Keywords: ATM inhibition; Metabolic reprogrammer; Mitochondria; P53; Senescence alleviation
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Year: 2020 PMID: 32949791 DOI: 10.1016/j.mito.2020.09.002
Source DB: PubMed Journal: Mitochondrion ISSN: 1567-7249 Impact factor: 4.160