Meng Qingfei, Zhang Yanghe, Hao Shiming, Sun Huihui, Liu Bin, Zhou Honglan, Wang Yishu, Xu Zhi-Xiang
Key Laboratory of Pathobiology, Ministry of Education, Jilin University, Changchun, China.
Department of Urology, The First Hospital of Jilin University, Changchun, China.
Front Pharmacol. 2022 Aug 24;13:932154. doi: 10.3389/fphar.2022.932154. eCollection 2022.
Glucose-6-phosphate dehydrogenase (G6PD) is the only rate-limiting enzyme in the pentose phosphate pathway (PPP). Rapidly proliferating cells require metabolites from PPP to synthesize ribonucleotides and maintain intracellular redox homeostasis. G6PD expression can be abnormally elevated in a variety of cancers. In addition, G6PD may act as a regulator of viral replication and vascular smooth muscle function. Therefore, G6PD-mediated activation of PPP may promote tumor and non-neoplastic disease progression. Recently, studies have identified post-translational modifications (PTMs) as an important mechanism for regulating G6PD function. Here, we provide a comprehensive review of various PTMs (e.g., phosphorylation, acetylation, glycosylation, ubiquitination, and glutarylation), which are identified in the regulation of G6PD structure, expression and enzymatic activity. In addition, we review signaling pathways that regulate G6PD and evaluate the role of oncogenic signals that lead to the reprogramming of PPP in tumor and non-neoplastic diseases as well as summarize the inhibitors that target G6PD.
葡萄糖-6-磷酸脱氢酶(G6PD)是磷酸戊糖途径(PPP)中唯一的限速酶。快速增殖的细胞需要PPP的代谢产物来合成核糖核苷酸并维持细胞内氧化还原稳态。G6PD的表达在多种癌症中可能异常升高。此外,G6PD可能作为病毒复制和血管平滑肌功能的调节剂。因此,G6PD介导的PPP激活可能促进肿瘤和非肿瘤性疾病的进展。最近,研究已确定翻译后修饰(PTM)是调节G6PD功能的重要机制。在此,我们全面综述了在G6PD结构、表达和酶活性调节中所确定的各种PTM(如磷酸化、乙酰化、糖基化、泛素化和戊二酰化)。此外,我们综述了调节G6PD的信号通路,并评估致癌信号在肿瘤和非肿瘤性疾病中导致PPP重编程的作用,以及总结靶向G6PD的抑制剂。