Inhibition of mutant EGFR in lung cancer cells triggers SOX2-FOXO6-dependent survival pathways

Elife. 2015 Feb 16:4:e06132. doi: 10.7554/eLife.06132.

Abstract

Treatment of EGFR-mutant lung cancer with erlotinib results in dramatic tumor regression but it is invariably followed by drug resistance. In characterizing early transcriptional changes following drug treatment of mutant EGFR-addicted cells, we identified the stem cell transcriptional regulator SOX2 as being rapidly and specifically induced, both in vitro and in vivo. Suppression of SOX2 sensitizes cells to erlotinib-mediated apoptosis, ultimately decreasing the emergence of acquired resistance, whereas its ectopic expression reduces drug-induced cell death. We show that erlotinib relieves EGFR-dependent suppression of FOXO6, leading to its induction of SOX2, which in turn represses the pro-apoptotic BH3-only genes BIM and BMF. Together, these observations point to a physiological feedback mechanism that attenuates oncogene addiction-mediated cell death associated with the withdrawal of growth factor signaling and may therefore contribute to the development of resistance.

Keywords: EGFR mutations; SOX2; human; human biology; lung cancer; medicine; mouse; resistance; targeted cancer therapy.

Publication types

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

MeSH terms

  • Adaptor Proteins, Signal Transducing / physiology
  • Apoptosis / drug effects
  • Apoptosis Regulatory Proteins / physiology
  • Bcl-2-Like Protein 11
  • Cell Line, Tumor
  • Cell Survival / physiology*
  • ErbB Receptors / antagonists & inhibitors*
  • ErbB Receptors / genetics
  • Erlotinib Hydrochloride / pharmacology
  • Forkhead Transcription Factors / physiology*
  • Humans
  • Lung Neoplasms / metabolism*
  • Membrane Proteins / physiology
  • Proto-Oncogene Proteins / physiology
  • SOXB1 Transcription Factors / physiology*

Substances

  • Adaptor Proteins, Signal Transducing
  • Apoptosis Regulatory Proteins
  • BCL2L11 protein, human
  • BMF protein, human
  • Bcl-2-Like Protein 11
  • Bcl2l11 protein, mouse
  • FOXO6 protein, human
  • Forkhead Transcription Factors
  • Membrane Proteins
  • Proto-Oncogene Proteins
  • SOX2 protein, human
  • SOXB1 Transcription Factors
  • Erlotinib Hydrochloride
  • ErbB Receptors