a Department of Morphology, Surgery and Experimental Medicine, Section of Pathology, Oncology and Experimental Biology , Laboratory for Technologies of Advanced Therapies (LTTA), University of Ferrara , Ferrara , Italy.
b Department of Clinical and Molecular Sciences, Polytechnical University of Marche , Ancona , Italy.
Cell Cycle. 2019 May;18(10):1068-1083. doi: 10.1080/15384101.2019.1612698. Epub 2019 May 10.
Aberrations in mitochondrial Ca homeostasis have been associated with different pathological conditions, including neurological defects, cardiovascular diseases, and, in the last years, cancer. With the recent molecular identification of the mitochondrial calcium uniporter (MCU) complex, the channel that allows Ca accumulation into the mitochondrial matrix, alterations in the expression levels or functioning in one or more MCU complex members have been linked to different cancers and cancer-related phenotypes. In this review, we will analyze the role of the uniporter and mitochondrial Ca derangements in modulating cancer cell sensitivity to death, invasiveness, and migratory capacity, as well as cancer progression in vivo. We will also discuss some critical points and contradictory results to highlight the consequence of MCU complex modulation in tumor development.
线粒体钙稳态的异常与多种病理状况有关,包括神经缺陷、心血管疾病,以及近年来的癌症。随着最近对线粒体钙单向转运蛋白(MCU)复合物的分子鉴定,即允许 Ca 积累到线粒体基质的通道,一个或多个 MCU 复合物成员的表达水平或功能的改变与不同的癌症和与癌症相关的表型有关。在这篇综述中,我们将分析单向转运蛋白和线粒体 Ca 紊乱在调节癌细胞对死亡、侵袭和迁移能力的敏感性,以及体内癌症进展中的作用。我们还将讨论一些关键点和矛盾的结果,以突出 MCU 复合物调节在肿瘤发展中的后果。