Laboratory of Health Chemistry, Graduate School of Pharmaceutical Sciences, Tohoku University, Sendai 980-8578, Japan.
Proc Natl Acad Sci U S A. 2023 Oct 24;120(43):e2311282120. doi: 10.1073/pnas.2311282120. Epub 2023 Oct 17.
Liquid droplet has emerged as a flexible intracellular compartment that modulates various 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 overridden 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.
液滴已成为调节各种细胞过程的灵活细胞内隔室。在这里,我们揭示了一种由 SQSTM1/p62 和 BRCA1 基因 1 邻居(NBR1)通过液-液相分离(LLPS)形成的液滴控制的抗转移机制。一些酪氨酸激酶抑制剂(TKIs)引发溶酶体应激反应,促进 p62 和 NBR1 的 LLPS,导致 p62/NBR1 液滴的扩散。有趣的是,在 p62/NBR1 液滴中,细胞凋亡蛋白 1 加速了 RAS 相关 C3 肉毒杆菌毒素底物 1 的降解,从而限制了癌细胞的运动性。此外,在体外和体内,p62/NBR1 双敲除细胞完全消除了 TKIs 的抗转移活性。因此,我们的结果表明 p62/NBR1 液滴作为癌细胞行为的关键决定因素的功能,这可能为 LLPS 的临床和生物学意义提供新的见解。