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靶向SREBP-1驱动的脂质代谢以治疗癌症。

Targeting SREBP-1-driven lipid metabolism to treat cancer.

作者信息

Guo Deliang, Bell Erica Hlavin, Mischel Paul, Chakravarti Arnab

机构信息

Department of Radiation Oncology, Ohio State University Comprehensive Cancer Center and Arthur G. James Cancer Hospital, Columbus, OH 43210, USA.

出版信息

Curr Pharm Des. 2014;20(15):2619-26. doi: 10.2174/13816128113199990486.

Abstract

Metabolic reprogramming is a hallmark of cancer. Oncogenic growth signaling regulates glucose, glutamine and lipid metabolism to meet the bioenergetics and biosynthetic demands of rapidly proliferating tumor cells. Emerging evidence indicates that sterol regulatory element-binding protein 1 (SREBP-1), a master transcription factor that controls lipid metabolism, is a critical link between oncogenic signaling and tumor metabolism. We recently demonstrated that SREBP-1 is required for the survival of mutant EGFR-containing glioblastoma, and that this pro-survival metabolic pathway is mediated, in part, by SREBP-1-dependent upregulation of the fatty acid synthesis and low density lipoprotein (LDL) receptor (LDLR). These results have identified EGFR/PI3K/Akt/SREBP-1 signaling pathway that promotes growth and survival in glioblastoma, and potentially other cancer types. Here, we summarize recent insights in the understanding of cancer lipid metabolism, and discuss the evidence linking SREBP-1 with PI3K/Akt signaling-controlled glycolysis and with Myc-regulated glutaminolysis to lipid metabolism. We also discuss the development of potential drugs targeting the SREBP-1- driven lipid metabolism as anti-cancer agents.

摘要

代谢重编程是癌症的一个标志。致癌生长信号调节葡萄糖、谷氨酰胺和脂质代谢,以满足快速增殖的肿瘤细胞的生物能量和生物合成需求。新出现的证据表明,固醇调节元件结合蛋白1(SREBP-1)是一种控制脂质代谢的主要转录因子,是致癌信号与肿瘤代谢之间的关键联系。我们最近证明,SREBP-1是含突变表皮生长因子受体(EGFR)的胶质母细胞瘤存活所必需的,并且这种促存活代谢途径部分是由SREBP-1依赖的脂肪酸合成上调和低密度脂蛋白(LDL)受体(LDLR)介导的。这些结果确定了EGFR/PI3K/Akt/SREBP-1信号通路,该通路促进胶质母细胞瘤以及可能其他癌症类型的生长和存活。在这里,我们总结了近期对癌症脂质代谢理解的见解,并讨论了将SREBP-1与PI3K/Akt信号控制的糖酵解以及与Myc调节的谷氨酰胺分解与脂质代谢联系起来的证据。我们还讨论了作为抗癌药物靶向SREBP-1驱动的脂质代谢的潜在药物的开发。

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