Literature DB >> 29480462

Role of p62 in the regulation of cell death induction.

Lihong Fan1, Shutao Yin2, Enxiang Zhang2, Hongbo Hu3.   

Abstract

p62 is a multifunctional adaptor protein implicated in various cellular processes. It has been found to regulate selective autophagy, cell survival, cell death, oxidative stress, DNA repair and inflammation, and to play a role in a number of diseases, such as tumourigenesis, Paget's disease of bone, neurodegenerative disease, diabetes, and obesity. Cell death induction is an important cellular process. The dysregulation of cell death induction is involved in the pathogenesis of various diseases, such as cancer, neurodegeneration diseases, and diabetes. In this review, we discuss the functional role of p62 in inducing cell death in response to multiple stimuli, and we summarize the potential signaling pathways that contribute to this regulation. Given the important role of p62 in regulating cell death, p62 is considered to be a reasonable target for managing cell death dysregulation-related pathogenic conditions. A better understanding of the role of p62 and its related mechanisms in regulating cell death is necessary for the more precise utilization of p62 as a target for treating relevant diseases.

Entities:  

Keywords:  Autophagy; Cell death; ER stress; NFκB; Nrf2; P62

Mesh:

Substances:

Year:  2018        PMID: 29480462     DOI: 10.1007/s10495-018-1445-z

Source DB:  PubMed          Journal:  Apoptosis        ISSN: 1360-8185            Impact factor:   4.677


  10 in total

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5.  Expression Analysis of Autophagy Related Markers LC3B, p62 and HMGB1 Indicate an Autophagy-Independent Negative Prognostic Impact of High p62 Expression in Pulmonary Squamous Cell Carcinomas.

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6.  p62 /SQSTM1 coding plasmid prevents age related macular degeneration in a rat model.

Authors:  Nataliya G Kolosova; Oyuna S Kozhevnikova; Darya V Telegina; Anzhela Zh Fursova; Natalia A Stefanova; Natalia A Muraleva; Franco Venanzi; Michael Y Sherman; Sergey I Kolesnikov; Albert A Sufianov; Vladimir L Gabai; Alexander M Shneider
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  10 in total

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