| Literature DB >> 33391038 |
Ying Wang1, Zhiwen Liu1, Shaoqun Shu1, Juan Cai1, Chengyuan Tang1, Zheng Dong1,2.
Abstract
Autophagy is a conserved, multistep pathway that degrades and recycles dysfunctional organelles and macromolecules to maintain cellular homeostasis. Mammalian target of rapamycin (mTOR) and adenosine-monophosphate activated-protein kinase (AMPK) are major negative and positive regulators of autophagy, respectively. In cisplatin-induced acute kidney injury (AKI) or nephrotoxicity, autophagy is rapidly induced in renal tubular epithelial cells and acts as a cytoprotective mechanism for cell survival. Both mTOR and AMPK have been implicated in the regulation of autophagy in cisplatin-induced AKI. Targeting mTOR and/or AMPK may offer effective strategies for kidney protection during cisplatin-mediated chemotherapy.Entities:
Keywords: AMPK; acute kidney injury; autophagy; cisplatin; mTOR; nephrotoxicity
Year: 2020 PMID: 33391038 PMCID: PMC7773913 DOI: 10.3389/fphys.2020.619730
Source DB: PubMed Journal: Front Physiol ISSN: 1664-042X Impact factor: 4.566