O‐GlcNAcylation promotes fatty acid synthase activity under nutritional stress as a pro‐survival mechanism in cancer cells

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 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]
卷期号:22 (9): e2100175-e2100175 被引量:22
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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