CEDOC, Chronic Diseases Research Centre, NOVA Medical School|Faculty of Medical Sciences, University NOVA of Lisbon, Campus dos Mártires da Pátria, 130, 1169-056 Lisbon, Portugal.
Institute of Oncology Francisco Gentil (IPOLFG), Rua Prof Lima Basto, 1099-023 Lisbon, Portugal.
Molecules. 2020 Sep 1;25(17):3984. doi: 10.3390/molecules25173984.
Metabolic remodeling is a critical skill of malignant cells, allowing their survival and spread. The metabolic dynamics and adaptation capacity of cancer cells allow them to escape from damaging stimuli, including breakage or cross-links in DNA strands and increased reactive oxygen species (ROS) levels, promoting resistance to currently available therapies, such as alkylating or oxidative agents. Therefore, it is essential to understand how metabolic pathways and the corresponding enzymatic systems can impact on tumor behavior. Cysteine aminotransferase (CAT) per se, as well as a component of the CAT: 3-mercaptopyruvate sulfurtransferase (MST) axis, is pivotal for this metabolic rewiring, constituting a central mechanism in amino acid metabolism and fulfilling the metabolic needs of cancer cells, thereby supplying other different pathways. In this review, we explore the current state-of-art on CAT function and its role on cancer cell metabolic rewiring as MST partner, and its relevance in cancer cells' fitness.
代谢重编程是恶性细胞的一项关键技能,使其能够存活和扩散。癌细胞的代谢动态和适应能力使它们能够逃避破坏性刺激,包括 DNA 链的断裂或交联以及活性氧 (ROS) 水平的升高,从而促进对现有治疗方法的耐药性,如烷化剂或氧化剂。因此,了解代谢途径和相应的酶系统如何影响肿瘤行为至关重要。半胱氨酸氨基转移酶 (CAT) 本身以及 CAT:3-巯基丙酮酸硫转移酶 (MST) 轴的一个组成部分,对于这种代谢重编程至关重要,构成了氨基酸代谢的核心机制,并满足了癌细胞的代谢需求,从而为其他不同的途径提供了支持。在这篇综述中,我们探讨了 CAT 功能的最新研究进展及其作为 MST 伴侣在癌细胞代谢重编程中的作用,以及其在癌细胞适应性方面的相关性。