自噬
磷脂酰肌醇
生物
激酶
细胞生物学
癌变
PI3K/AKT/mTOR通路
癌症
蛋白质亚单位
癌细胞
信号转导
癌症研究
生物化学
基因
遗传学
细胞凋亡
作者
Chien‐An Chu,Yi-Wen Wang,Yi-Lin Chen,Hui‐Wen Chen,Jing-Jing Chuang,Hong Chang,Chung‐Liang Ho,Chen Chang,Nan-Haw Chow,Chung-Ta Lee
标识
DOI:10.3390/ijms222010964
摘要
Phosphatidylinositol 3-kinase catalytic subunit type 3 (PIK3C3), the mammalian ortholog of yeast vesicular protein sorting 34 (Vps34), belongs to the phosphoinositide 3-kinase (PI3K) family. PIK3C3 can phosphorylate phosphatidylinositol (PtdIns) to generate phosphatidylinositol 3-phosphate (PI3P), a phospholipid central to autophagy. Inhibition of PIK3C3 successfully inhibits autophagy. Autophagy maintains cell survival when modifications occur in the cellular environment and helps tumor cells resist metabolic stress and cancer treatment. In addition, PIK3C3 could induce oncogenic transformation and enhance tumor cell proliferation, growth, and invasion through mechanisms independent of autophagy. This review addresses the structural and functional features, tissue distribution, and expression pattern of PIK3C3 in a variety of human tumors and highlights the underlying mechanisms involved in carcinogenesis. The implications in cancer biology, patient prognosis prediction, and cancer therapy are discussed. Altogether, the discovery of pharmacological inhibitors of PIK3C3 could reveal novel strategies for improving treatment outcomes for PIK3C3-mediated human diseases.
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