Your browser doesn't support javascript.
loading
Role of p62/SQSTM1 in liver physiology and pathogenesis.
Manley, Sharon; Williams, Jessica A; Ding, Wen-Xing.
Affiliation
  • Manley S; Department of Pharmacology, Toxicology and Therapeutics, University of Kansas Medical Center, Kansas City, USA.
Exp Biol Med (Maywood) ; 238(5): 525-38, 2013 May.
Article in En | MEDLINE | ID: mdl-23856904
ABSTRACT
p62/sequestosome-1/A170/ZIP (hereafter referred to as p62) is a scaffold protein that has multiple functions, such as signal transduction, cell proliferation, cell survival, cell death, inflammation, tumourigenesis and oxidative stress response. While p62 is an autophagy substrate and is degraded by autophagy, p62 serves as an autophagy receptor for selective autophagic clearance of protein aggregates and organelles. Moreover, p62 functions as a signalling hub for various signalling pathways, including NF-κB, Nrf2 and mTOR. In this review, we discuss the pathophysiological role of p62 in the liver, including formation of hepatic inclusion bodies, cholestasis, obesity, insulin resistance, liver cell death and tumourigenesis.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cell Transformation, Neoplastic / Adaptor Proteins, Signal Transducing / Liver / Liver Neoplasms / Neoplasm Proteins Type of study: Etiology_studies Limits: Animals / Humans Language: En Journal: Exp Biol Med (Maywood) Year: 2013 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cell Transformation, Neoplastic / Adaptor Proteins, Signal Transducing / Liver / Liver Neoplasms / Neoplasm Proteins Type of study: Etiology_studies Limits: Animals / Humans Language: En Journal: Exp Biol Med (Maywood) Year: 2013 Document type: Article