Literature DB >> 30588824

p62/SQSTM1 and Selective Autophagy in Cardiometabolic Diseases.

Se-Jin Jeong1, Xiangyu Zhang1, Astrid Rodriguez-Velez1, Trent D Evans1, Babak Razani1,2,3.   

Abstract

Significance: p62/SQSTM1 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. Critical Issues: 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. Recent Advances: This review first discusses the features that make p62/SQSTM1 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/SQSTM1. 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. Future Directions: A comprehensive understanding of the nuanced roles p62/SQSTM1 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.

Entities:  

Keywords:  atherosclerosis; cardiometabolic disease; cardiovascular disease; fatty liver disease; p62/; selective autophagy

Year:  2019        PMID: 30588824      PMCID: PMC6653798          DOI: 10.1089/ars.2018.7649

Source DB:  PubMed          Journal:  Antioxid Redox Signal        ISSN: 1523-0864            Impact factor:   8.401


  113 in total

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Journal:  J Biol Chem       Date:  2001-01-22       Impact factor: 5.157

2.  LC3, a mammalian homologue of yeast Apg8p, is localized in autophagosome membranes after processing.

Authors:  Y Kabeya; N Mizushima; T Ueno; A Yamamoto; T Kirisako; T Noda; E Kominami; Y Ohsumi; T Yoshimori
Journal:  EMBO J       Date:  2000-11-01       Impact factor: 11.598

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Review 4.  Role of the heat shock response and molecular chaperones in oncogenesis and cell death.

Authors:  C Jolly; R I Morimoto
Journal:  J Natl Cancer Inst       Date:  2000-10-04       Impact factor: 13.506

5.  The deacetylase HDAC6 regulates aggresome formation and cell viability in response to misfolded protein stress.

Authors:  Yoshiharu Kawaguchi; Jeffrey J Kovacs; Adam McLaurin; Jeffery M Vance; Akihiro Ito; Tso Pang Yao
Journal:  Cell       Date:  2003-12-12       Impact factor: 41.582

6.  The interaction of p62 with RIP links the atypical PKCs to NF-kappaB activation.

Authors:  L Sanz; P Sanchez; M J Lallena; M T Diaz-Meco; J Moscat
Journal:  EMBO J       Date:  1999-06-01       Impact factor: 11.598

7.  p62 Is a common component of cytoplasmic inclusions in protein aggregation diseases.

Authors:  Kurt Zatloukal; Cornelia Stumptner; Andrea Fuchsbichler; Hans Heid; Martina Schnoelzer; Lukas Kenner; Reinhold Kleinert; Marco Prinz; Adriano Aguzzi; Helmut Denk
Journal:  Am J Pathol       Date:  2002-01       Impact factor: 4.307

8.  Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase.

Authors:  H Shimura; N Hattori; S i Kubo; Y Mizuno; S Asakawa; S Minoshima; N Shimizu; K Iwai; T Chiba; K Tanaka; T Suzuki
Journal:  Nat Genet       Date:  2000-07       Impact factor: 38.330

9.  The human peroxisomal targeting signal receptor, Pex5p, is translocated into the peroxisomal matrix and recycled to the cytosol.

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Journal:  Cell       Date:  2001-04-20       Impact factor: 41.582

10.  The atypical PKC-interacting protein p62 is an important mediator of RANK-activated osteoclastogenesis.

Authors:  Angeles Durán; Manuel Serrano; Michael Leitges; Juana M Flores; Sylvain Picard; Jacques P Brown; Jorge Moscat; Maria T Diaz-Meco
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  17 in total

1.  A proteome-wide assessment of the oxidative stress paradigm for metal and metal-oxide nanomaterials in human macrophages.

Authors:  Tong Zhang; Matthew J Gaffrey; Dennis G Thomas; Thomas J Weber; Becky M Hess; Karl K Weitz; Paul D Piehowski; Vladislav A Petyuk; Ronald J Moore; Wei-Jun Qian; Brian D Thrall
Journal:  NanoImpact       Date:  2019-11-23

2.  BAG3 protects chondrocytes against lumbar facet joint osteoarthritis by regulating autophagy and apoptosis.

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3.  Cleavage of the selective autophagy receptor SQSTM1/p62 by the SARS-CoV-2 main protease NSP5 prevents the autophagic degradation of viral membrane proteins.

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Journal:  Mol Biomed       Date:  2022-06-03

Review 4.  Renal Cellular Autophagy in Obesity: Boon or Bane?

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Journal:  Semin Nephrol       Date:  2021-07       Impact factor: 4.472

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Journal:  Cell Death Dis       Date:  2019-08-13       Impact factor: 8.469

6.  Autophagy blockage promotes the pyroptosis of ox-LDL-treated macrophages by modulating the p62/Nrf2/ARE axis.

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7.  Berberine Reshapes the Balance of the Local Renin-Angiotensin System by Modulating Autophagy under Metabolic Stress in Pancreatic Islets.

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8.  Expression of Four Autophagy-Related Genes Accurately Predicts the Prognosis of Gastrointestinal Cancer in Asian Patients.

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Review 9.  The Role of HDAC6 in Autophagy and NLRP3 Inflammasome.

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Review 10.  Nuclear Receptors as Autophagy-Based Antimicrobial Therapeutics.

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Journal:  Cells       Date:  2020-08-27       Impact factor: 6.600

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