Machado Eda R, Annunziata Ida, van de Vlekkert Diantha, Grosveld Gerard C, d'Azzo Alessandra
Department of Genetics, St. Jude Children's Research Hospital, Memphis, TN, United States.
Department of Anatomy and Neurobiology, College of Graduate Health Sciences, University of Tennessee Health Science Center, Memphis, TN, United States.
Front Cell Dev Biol. 2021 Feb 26;9:642494. doi: 10.3389/fcell.2021.642494. eCollection 2021.
During primary tumorigenesis isolated cancer cells may undergo genetic or epigenetic changes that render them responsive to additional intrinsic or extrinsic cues, so that they enter a transitional state and eventually acquire an aggressive, metastatic phenotype. Among these changes is the alteration of the cell metabolic/catabolic machinery that creates the most permissive conditions for invasion, dissemination, and survival. The lysosomal system has emerged as a crucial player in this malignant transformation, making this system a potential therapeutic target in cancer. By virtue of their ubiquitous distribution in mammalian cells, their multifaced activities that control catabolic and anabolic processes, and their interplay with other organelles and the plasma membrane (PM), lysosomes function as platforms for inter- and intracellular communication. This is due to their capacity to adapt and sense nutrient availability, to spatially segregate specific functions depending on their position, to fuse with other compartments and with the PM, and to engage in membrane contact sites (MCS) with other organelles. Here we review the latest advances in our understanding of the role of the lysosomal system in cancer progression. We focus on how changes in lysosomal nutrient sensing, as well as lysosomal positioning, exocytosis, and fusion perturb the communication between tumor cells themselves and between tumor cells and their microenvironment. Finally, we describe the potential impact of MCS between lysosomes and other organelles in propelling cancer growth and spread.
在原发性肿瘤发生过程中,孤立的癌细胞可能会经历基因或表观遗传变化,使其对其他内在或外在信号产生反应,从而进入过渡状态并最终获得侵袭性的转移表型。这些变化包括细胞代谢/分解代谢机制的改变,这种改变为侵袭、扩散和存活创造了最有利的条件。溶酶体系统已成为这种恶性转化的关键参与者,使该系统成为癌症潜在的治疗靶点。由于溶酶体在哺乳动物细胞中广泛分布,具有控制分解代谢和合成代谢过程的多方面活性,以及与其他细胞器和质膜(PM)的相互作用,溶酶体充当细胞间和细胞内通讯的平台。这是因为它们能够适应和感知营养物质的可用性,根据其位置在空间上分隔特定功能,与其他区室和质膜融合,并与其他细胞器形成膜接触位点(MCS)。在这里,我们综述了我们对溶酶体系统在癌症进展中作用的最新认识进展。我们关注溶酶体营养感知的变化,以及溶酶体定位、胞吐作用和融合如何扰乱肿瘤细胞自身之间以及肿瘤细胞与其微环境之间的通讯。最后,我们描述了溶酶体与其他细胞器之间的膜接触位点在推动癌症生长和扩散方面的潜在影响。