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miR-29对SCAP/SREBP-1的反馈环调节作用调控表皮生长因子受体信号驱动的胶质母细胞瘤生长。

Feedback Loop Regulation of SCAP/SREBP-1 by miR-29 Modulates EGFR Signaling-Driven Glioblastoma Growth.

作者信息

Ru Peng, Hu Peng, Geng Feng, Mo Xiaokui, Cheng Chunming, Yoo Ji Young, Cheng Xiang, Wu Xiaoning, Guo Jeffrey Yunhua, Nakano Ichiro, Lefai Etienne, Kaur Balveen, Chakravarti Arnab, Guo Deliang

机构信息

Department of Radiation Oncology, James Comprehensive Cancer Center, College of Medicine, The Ohio State University, Columbus, OH 43210, USA.

Center for Biostatistics, Department of Bioinformatics, College of Medicine, The Ohio State University, Columbus, OH 43210, USA.

出版信息

Cell Rep. 2016 Aug 9;16(6):1527-1535. doi: 10.1016/j.celrep.2016.07.017. Epub 2016 Jul 28.

Abstract

Dysregulated lipid metabolism is a characteristic of malignancies. Sterol regulatory element binding protein 1 (SREBP-1), a transcription factor playing a central role in lipid metabolism, is highly activated in malignancies. Here, we unraveled a link between miR-29 and the SCAP (SREBP cleavage-activating protein)/SREBP-1 pathway in glioblastoma (GBM) growth. Epidermal growth factor receptor (EGFR) signaling enhances miR-29 expression in GBM cells via upregulation of SCAP/SREBP-1, and SREBP-1 activates miR-29 expression via binding to specific sites in its promoter. In turn, miR-29 inhibits SCAP and SREBP-1 expression by interacting with their 3' UTRs. miR-29 transfection suppressed lipid synthesis and GBM cell growth, which were rescued by the addition of fatty acids or N-terminal SREBP-1 expression. Xenograft studies showed that miR-29 mimics significantly inhibit GBM growth and prolong the survival of GBM-bearing mice. Our study reveals a previously unrecognized negative feedback loop in SCAP/SREBP-1 signaling mediated by miR-29 and suggests that miR-29 treatment may represent an effective means to target GBM.

摘要

脂质代谢失调是恶性肿瘤的一个特征。固醇调节元件结合蛋白1(SREBP-1)是一种在脂质代谢中起核心作用的转录因子,在恶性肿瘤中高度激活。在此,我们揭示了miR-29与胶质母细胞瘤(GBM)生长中SCAP(SREBP裂解激活蛋白)/SREBP-1途径之间的联系。表皮生长因子受体(EGFR)信号通过上调SCAP/SREBP-1增强GBM细胞中miR-29的表达,而SREBP-1通过与其启动子中的特定位点结合激活miR-29的表达。反过来,miR-29通过与其3'UTR相互作用抑制SCAP和SREBP-1的表达。miR-29转染抑制脂质合成和GBM细胞生长,添加脂肪酸或N端SREBP-1表达可挽救这种抑制作用。异种移植研究表明,miR-29模拟物显著抑制GBM生长并延长荷GBM小鼠的生存期。我们的研究揭示了miR-29介导的SCAP/SREBP-1信号中一个以前未被认识的负反馈环,并表明miR-29治疗可能是靶向GBM的一种有效手段。

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