| Literature DB >> 27477273 |
Peng Ru1, Peng Hu1, Feng Geng1, Xiaokui Mo2, Chunming Cheng1, Ji Young Yoo3, Xiang Cheng1, Xiaoning Wu1, Jeffrey Yunhua Guo4, Ichiro Nakano5, Etienne Lefai6, Balveen Kaur3, Arnab Chakravarti1, Deliang Guo7.
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.Entities:
Keywords: EGFR; SCAP; SREBP-1; glioblastoma; lipid metabolism; miR-29
Mesh:
Substances:
Year: 2016 PMID: 27477273 PMCID: PMC4981543 DOI: 10.1016/j.celrep.2016.07.017
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423