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p62/ and Selective Autophagy in Cardiometabolic Diseases.

Citation
Jeong, S. -J., et al. “P62/ And Selective Autophagy In Cardiometabolic Diseases.”. Antioxidants & Redox Signaling, pp. 458-471.
Center Washington University in St Louis
Author Se-Jin Jeong, Xiangyu Zhang, Astrid Rodriguez-Velez, Trent D Evans, Babak Razani
Keywords atherosclerosis, cardiometabolic disease, Cardiovascular disease, fatty liver disease, p62/, selective autophagy
Abstract

p62/ is a multifunctional scaffolding protein involved in the regulation of various signaling pathways as well as autophagy. In particular, p62/SQSTM1 serves as an essential adaptor to identify and deliver specific organelles and protein aggregates to autophagosomes for degradation, a process known as selective autophagy. With the emergence of autophagy as a critical process in cellular metabolism and the development of cardiometabolic diseases, it is increasingly important to understand p62's role in the integration of signaling and autophagic pathways. This review first discusses the features that make p62/ an ideal chaperone in integrating signaling pathways with autophagy and details the current understanding of its diverse roles in selective autophagy processes. Distinct and overlapping roles of other chaperones with similar functions are then discussed in the context of p62/. Finally, the recent literature focusing on p62 and selective autophagy in metabolism and the spectrum of cardiometabolic diseases including atherosclerosis, fatty liver disease, and obesity is evaluated. A comprehensive understanding of the nuanced roles p62/ plays in mediating distinct autophagy pathways would provide new insights into the mechanisms of this critical degradative pathway. This will, in turn, facilitate our understanding of cardiovascular and cardiometabolic disease pathology and the development of novel autophagy-modulating therapeutic strategies.

Year of Publication
2019
Journal
Antioxidants & redox signaling
Volume
31
Issue
6
Number of Pages
458-471
Date Published
12/2019
ISSN Number
1557-7716
DOI
10.1089/ars.2018.7649
Alternate Journal
Antioxid. Redox Signal.
PMID
30588824
PMCID
PMC6653798
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