LLPS of SQSTM1/p62 and NBR1 as outcomes of lysosomal stress response limits cancer cell metastasis

被引:21
作者
Noguchi, Takuya [1 ]
Sekiguchi, Yuto [1 ]
Shimada, Tatsuya [1 ]
Suzuki, Wakana [1 ]
Yokosawa, Takumi [1 ]
Itoh, Tamaki [1 ]
Yamada, Mayuka [1 ]
Suzuki, Midori [1 ]
Kurokawa, Reon [1 ]
Hirata, Yusuke [1 ]
Matsuzawa, Atsushi [1 ]
机构
[1] Tohoku Univ, Grad Sch Pharmaceut Sci, Lab Hlth Chem, Sendai 9808578, Japan
基金
日本学术振兴会;
关键词
p62; NBR1; LLPS; cancer metastasis; lysosomal stress; PHASE-SEPARATION; SELECTIVE AUTOPHAGY; IAP PROTEINS; P62; MIGRATION; CIAP1; APOPTOSIS; PHOSPHORYLATION; AMPLIFICATION; AGGREGATION;
D O I
10.1073/pnas.2311282120
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Liquid droplet has emerged as a flexible intracellular compartment that modulates var-ious cellular processes. Here, we uncover an antimetastatic mechanism governed by the liquid droplets formed through liquid-liquid phase separation (LLPS) of SQSTM1/ p62 and neighbor of BRCA1 gene 1 (NBR1). Some of the tyrosine kinase inhibitors (TKIs) initiated lysosomal stress response that promotes the LLPS of p62 and NBR1, resulting in the spreading of p62/NBR1 liquid droplets. Interestingly, in the p62/ NBR1 liquid droplet, degradation of RAS- related C3 botulinum toxin substrate 1 was accelerated by cellular inhibitor of apoptosis protein 1, which limits cancer cell motility. Moreover, the antimetastatic activity of the TKIs was completely overrid-den in p62/NBR1 double knockout cells both in vitro and in vivo. Thus, our results demonstrate a function of the p62/NBR1 liquid droplet as a critical determinant of cancer cell behavior, which may provide insight into both the clinical and biological significance of LLPS.
引用
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页数:12
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