Women's Malignancies Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD, 20892, USA.
Br J Cancer. 2021 Jan;124(1):66-75. doi: 10.1038/s41416-020-01179-8. Epub 2020 Dec 2.
A potentially important aspect in the regulation of tumour metastasis is endocytosis. This process consists of internalisation of cell-surface receptors via pinocytosis, phagocytosis or receptor-mediated endocytosis, the latter of which includes clathrin-, caveolae- and non-clathrin or caveolae-mediated mechanisms. Endocytosis then progresses through several intracellular compartments for sorting and routing of cargo, ending in lysosomal degradation, recycling back to the cell surface or secretion. Multiple endocytic proteins are dysregulated in cancer and regulate tumour metastasis, particularly migration and invasion. Importantly, four metastasis suppressor genes function in part by regulating endocytosis, namely, the NME, KAI, MTSS1 and KISS1 pathways. Data on metastasis suppressors identify a new point of dysregulation operative in tumour metastasis, alterations in signalling through endocytosis. This review will focus on the multicomponent process of endocytosis affecting different steps of metastasis and how metastatic-suppressor genes use endocytosis to suppress metastasis.
肿瘤转移调控中一个潜在的重要方面是内吞作用。该过程通过胞饮作用、吞噬作用或受体介导的内吞作用将细胞表面受体内化,后者包括网格蛋白、小窝蛋白和非网格蛋白或小窝蛋白介导的机制。内吞作用然后通过几个细胞内隔室进行货物的分拣和路由,最终在溶酶体降解、回收回细胞表面或分泌。在癌症中,多种内吞作用蛋白失调并调节肿瘤转移,特别是迁移和侵袭。重要的是,四个转移抑制基因部分通过调节内吞作用发挥作用,即 NME、KAI、MTSS1 和 KISS1 途径。关于转移抑制物的数据确定了肿瘤转移中作用的新失调点,即通过内吞作用改变信号转导。这篇综述将重点介绍影响转移不同步骤的多成分内吞作用过程,以及转移性抑制基因如何利用内吞作用抑制转移。