Cell Reports (Aug 2016)

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

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

DOI
https://doi.org/10.1016/j.celrep.2016.07.017
Journal volume & issue
Vol. 16, no. 6
pp. 1527 – 1535

Abstract

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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.

Keywords