Literature DB >> 28966079

Multifunctional p62 Effects Underlie Diverse Metabolic Diseases.

Min Long1, Xing Li1, Li Li1, Matthew Dodson2, Donna D Zhang2, Hongting Zheng3.   

Abstract

p62, a protein capable of binding both ubiquitin and autophagy substrates, is well established as a key regulator in cancer and neurodegenerative diseases. Recently, there has been accumulating evidence that p62 is also a pivotal regulator in metabolic diseases, such as obesity, T2DM, NAFLD, metabolic bone disease, gout and thyroid disease. This review summarizes the emerging role of p62 on these diseases by considering its functional domains, phenotypes in genetically modified animals, clinically observed alterations, and its effects on downstream metabolic signaling pathways. At the same time, we highlight the need to explore the roles played by p62 in the gastrointestinal environment and immune system, and the extent to which its elevated expression may confer protection against metabolic disorders.
Copyright © 2017 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  autophagy; autophagy-independent; metabolic diseases; p62; sequestosome1 (SQSTM1)

Mesh:

Substances:

Year:  2017        PMID: 28966079     DOI: 10.1016/j.tem.2017.09.001

Source DB:  PubMed          Journal:  Trends Endocrinol Metab        ISSN: 1043-2760            Impact factor:   12.015


  13 in total

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