Brain Tumor Center and Department of Neuro-Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA; Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA; Cancer Biology Program, MD Anderson Cancer Center UTHealth Graduate School of Biomedical Sciences, The University of Texas, Houston, TX 77030, USA.
Molecular and Cell Biology Laboratory, Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Trends Biochem Sci. 2018 Apr;43(4):301-310. doi: 10.1016/j.tibs.2018.01.006. Epub 2018 Feb 17.
Protein kinases regulate every aspect of cellular activity, whereas metabolic enzymes are responsible for energy production and catabolic and anabolic processes. Emerging evidence demonstrates that some metabolic enzymes, such as pyruvate kinase M2 (PKM2), phosphoglycerate kinase 1 (PGK1), ketohexokinase (KHK) isoform A (KHK-A), hexokinase (HK), and nucleoside diphosphate kinase 1 and 2 (NME1/2), that phosphorylate soluble metabolites can also function as protein kinases and phosphorylate a variety of protein substrates to regulate the Warburg effect, gene expression, cell cycle progression and proliferation, apoptosis, autophagy, exosome secretion, T cell activation, iron transport, ion channel opening, and many other fundamental cellular functions. The elevated protein kinase functions of these moonlighting metabolic enzymes in tumor development make them promising therapeutic targets for cancer.
蛋白激酶调节细胞活动的各个方面,而代谢酶则负责能量产生以及分解代谢和合成代谢过程。新出现的证据表明,一些代谢酶,如丙酮酸激酶 M2(PKM2)、磷酸甘油酸激酶 1(PGK1)、己酮激酶(KHK)同工型 A(KHK-A)、己糖激酶(HK)和核苷二磷酸激酶 1 和 2(NME1/2),能够磷酸化可溶性代谢物,它们也可以作为蛋白激酶发挥作用,磷酸化多种蛋白底物,从而调节瓦伯格效应、基因表达、细胞周期进程和增殖、细胞凋亡、自噬、外泌体分泌、T 细胞激活、铁转运、离子通道开放以及许多其他基本的细胞功能。这些代谢酶的蛋白激酶功能在肿瘤发生中升高,使它们成为癌症有前途的治疗靶点。