p62/SQSTM1: 'Jack of all trades' in health and cancer

被引:198
作者
Sanchez-Martin, Pablo [1 ]
Saito, Tetsuya [1 ]
Komatsu, Masaaki [1 ,2 ]
机构
[1] Niigata Univ, Dept Biochem, Grad Sch Med & Dent Sci, Niigata, Japan
[2] Juntendo Univ, Grad Sch Med, Dept Physiol, Tokyo, Japan
基金
日本学术振兴会;
关键词
autophagy; cancer; Keap1; mTORC1; NF-kappa B; Nrf2; p62/SQSTM1; NF-KAPPA-B; TRANSCRIPTION FACTOR NRF2; SELECTIVE AUTOPHAGY SUBSTRATE; POOR-PROGNOSIS; UBA DOMAIN; HEPATOCELLULAR-CARCINOMA; UBIQUITIN-BINDING; PROTEIN P62; BECLIN; ACTIVATION;
D O I
10.1111/febs.14712
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
p62 is a stress-inducible protein able to change among binding partners, cellular localizations and form liquid droplet structures in a context-dependent manner. This protein is mainly defined as a cargo receptor for selective autophagy, a process that allows the degradation of detrimental and unnecessary components through the lysosome. Besides this role, its ability to interact with multiple binding partners allows p62 to act as a main regulator of the activation of the Nrf2, mTORC1, and NF-kappa B signaling pathways, linking p62 to the oxidative defense system, nutrient sensing, and inflammation, respectively. In the present review, we will present the molecular mechanisms behind the control p62 exerts over these pathways, their interconnection and how their deregulation contributes to cancer progression.
引用
收藏
页码:8 / 23
页数:16
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