Growth factor receptor signaling induces mitophagy through epitranscriptomic regulation

Autophagy. 2023 Mar;19(3):1034-1035. doi: 10.1080/15548627.2022.2114765. Epub 2022 Aug 22.

Abstract

Aberrant growth factor receptor signaling is among the most common oncogenic drivers in cancer biology. Receptor signaling classically induces cancer growth through signaling cascades that mediate effects largely through transcriptional control. Recently, post-transcriptional RNA modifications, collectively designated as epitranscriptomics, have emerged as a critical layer of dysregulation in cancer biology. We recently reported that PDGFR (platelet-derived growth factor receptor) activity in cancer stem cells (CSCs) derived from glioblastoma patients displays increased post-transcriptional mRNA methylation (N6-methyladenosine [m6A]), which promotes CSC maintenance through regulation of mitophagy. Specifically, PDGF-PDGFRB signaling upregulates the expression of the m6A methyltransferase METTL3, which then decorates the mitophagy regulator OPTN (optineurin) mRNA with m6A, thereby promoting OPTN mRNA degradation. Glioblastomas express lower levels of OPTN than normal brain, and forced expression of OPTN reduces tumor growth, supporting a tumor suppressive role for OPTN. Pharmacological targeting of METTL3 with PDGFR or activation of mitophagy demonstrates a combinatorial benefit. Collectively, our results suggest that upstream regulation of mitophagy in lethal cancers is mediated through growth factor receptor control of post-transcriptional RNA regulation, offering novel therapeutic paradigms.

Keywords: Cancer stem cell; Glioblastoma; Mitophagy; N6-methyladenosine (m6A); OPTN; PDGFR.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Autophagy*
  • Humans
  • Methyltransferases / metabolism
  • Mitophagy*
  • RNA, Messenger / genetics
  • Receptors, Growth Factor
  • Signal Transduction

Substances

  • Receptors, Growth Factor
  • RNA, Messenger
  • METTL3 protein, human
  • Methyltransferases