巴基斯坦卢比
丙酮酸激酶
糖酵解
相扑蛋白
癌症研究
丙酮酸脱氢酶激酶
丙酮酸脱氢酶复合物
生物
肝细胞癌
激酶
蛋白激酶A
厌氧糖酵解
细胞生物学
生物化学
化学
泛素
酶
基因
作者
Zhao Chunlian,Qi Wan,Rui Zhao
摘要
Hepatocellular carcinoma (HCC) is one of the deadly malignant tumors that directly leads to the death of nearly one million people worldwide every year, causing a serious burden on society. In the presence of sufficient oxygen, HCC cells rapidly generate energy through aerobic glycolysis, which promotes tumor cell proliferation, immune evasion, metastasis, angiogenesis, and drug resistance. Pyruvate kinase M2 (PKM2) is a key rate-limiting enzyme in glycolysis. In recent years, studies have found that PKM2 not only exerts pyruvate kinase activity in the process of glucose metabolism, but also exerts protein kinase activity in non-metabolic pathways to affect tumor cell processes, and its activity is flexibly regulated by various posttranslational modifications such as acetylation, phosphorylation, lactylation, ubiquitination, SUMOylation, and so forth. This review summarizes the role of posttranslational modifications of PKM2-related sites in the development of HCC.
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