磷酸甘油酸激酶 1:癌症的有效治疗靶点

IF 3.3 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Frontiers in bioscience (Landmark edition) Pub Date : 2024-03-06 DOI:10.31083/j.fbl2903092
Ailin Qiu, Xiaosha Wen, Qingshuang Zou, Lei Yin, Siqi Zhu, Yao Sheng, Yan He, Quan Liu, Dixian Luo, Zifen Guo
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引用次数: 0

摘要

磷酸甘油酸激酶 1(PGK1)是细胞糖酵解途径中的一种关键酶,可促进肿瘤细胞中三磷酸腺苷(ATP)的生成并推动沃伯格效应。PGK1 通过将 1,3-二磷酸甘油酯(1,3-BPG)转化为腺苷-5'-二磷酸镁(Mg-ADP)的可逆磷酸化反应生成 ATP。除了调节细胞新陈代谢的作用外,PGK1 还在诱导自噬、调节三羧酸循环(TCA)以及包括肿瘤细胞耐药性在内的各种机制中发挥着关键作用。鉴于 PGK1 在细胞内的多方面功能,它与乳腺癌、星形细胞瘤、转移性结肠癌和胰腺导管腺癌等多种癌症的关系错综复杂。值得注意的是,PGK1 可作为细胞内蛋白激酶发挥作用,通过翻译后修饰(PTM)协调肿瘤的生长、迁移和侵袭。此外,在癌症组织中已观察到 PGK1 的表达水平升高,这表明它与不利的治疗结果和预后有关。本综述全面总结了 PGK1 的表达模式、结构特征、功能特性、参与 PTMs 以及与肿瘤的相互作用。此外,还重点介绍了开发和应用相关抑制剂的前景,证实了 PGK1 在肿瘤进展中不可或缺的价值。
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Phosphoglycerate Kinase 1: An Effective Therapeutic Target in Cancer.

Phosphoglycerate kinase 1 (PGK1) serves as a pivotal enzyme in the cellular glycolysis pathway, facilitating adenosine-triphosphate (ATP) production in tumor cells and driving the Warburg effect. PGK1 generates ATP through the reversible phosphorylation reaction of 1,3-bisphosphoglycerate (1,3-BPG) to Mg-adenosine-5'-diphosphate (Mg-ADP). In addition to its role in regulating cellular metabolism, PGK1 plays a pivotal role in autophagy induction, regulation of the tricarboxylic acid cycle (TCA), and various mechanisms including tumor cell drug resistance, and so on. Given its multifaceted functions within cells, the involvement of PGK1 in many types of cancer, including breast cancer, astrocytoma, metastatic colon cancer, and pancreatic ductal adenocarcinoma, is intricate. Notably, PGK1 can function as an intracellular protein kinase to coordinate tumor growth, migration, and invasion via posttranslational modifications (PTMs). Furthermore, elevated expression levels of PGK1 have been observed in cancer tissues, indicating its association with unfavorable treatment outcomes and prognosis. This review provides a comprehensive summary of PGK1's expression pattern, structural features, functional properties, involvement in PTMs, and interaction with tumors. Additionally highlighted are the prospects for developing and applying related inhibitors that confirm the indispensable value of PGK1 in tumor progression.

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