脂肪酸合酶
蛋白质组学
脂肪酸代谢
脂肪酸合成
糖基化
脂肪酸
生物化学
癌细胞
机制(生物学)
癌症
生物
赫拉
体外
酶
脂肪酸结合蛋白
细胞生物学
基因
认识论
哲学
遗传学
作者
Yin‐Kwan Wong,Jigang Wang,Teck Kwang Lim,Qingsong Lin,Celestial T. Yap,Han‐Ming Shen
出处
期刊:Proteomics
[Wiley]
日期:2022-02-09
卷期号:22 (9)
被引量:5
标识
DOI:10.1002/pmic.202100175
摘要
Protein O-GlcNAcylation is a specific form of protein glycosylation that targets a wide range of proteins with important functions. O-GlcNAcylation is known to be deregulated in cancer and has been linked to multiple aspects of cancer pathology. Despite its ubiquity and importance, the current understanding of the role of O-GlcNAcylation in the stress response remains limited. In this study, we performed a quantitative chemical proteomics-based open study of the O-GlcNAcome in HeLa cells, and identified 163 differentially-glycosylated proteins under starvation, involving multiple metabolic pathways. Among them, fatty acid metabolism was found to be targeted and subsequent analysis confirmed that fatty acid synthase (FASN) is O-GlcNAcylated. O-GlcNAcylation led to enhanced de novo fatty acid synthesis (FAS) activity, and fatty acids contributed to the cytoprotective effects of O-GlcNAcylation under starvation. Moreover, dual inhibition of O-GlcNAcylation and FASN displayed a strong synergistic effect in vitro in inducing cell death in cancer cells. Together, the results from this study provide novel insights into the role of O-GlcNAcylation in the nutritional stress response and suggest the potential of combining inhibition of O-GlcNAcylation and FAS in cancer therapy.
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