mTORC 2:1 for chemotherapy sensitization in glioblastoma

Cancer Discov. 2011 Nov;1(6):475-6. doi: 10.1158/2159-8290.CD-11-0264.

Abstract

mTOR signaling is frequently deregulated in cancer, including brain tumors. Although the signaling of mTOR complex 1 (mTORC1) has been subject to intensive investigations and mTORC1 itself has been a well-established cancer drug target for years, the role of the second complex, mTORC2, remains elusive. Tanaka et al. reveal an EGFRvIII-mTORC2-NFκB signaling cascade and demonstrate that mTORC2 mediates cisplatin resistance through NF-κB in an Akt-independent manner in glioblastoma. Uncovering the role of mTORC2 in chemotherapy resistance in glioblastoma highlights the need for further investigations of mTORC2 inhibition.

Publication types

  • Comment

MeSH terms

  • Brain Neoplasms / metabolism*
  • ErbB Receptors / metabolism*
  • Glioblastoma / metabolism*
  • Humans
  • NF-kappa B / metabolism*
  • Transcription Factors / metabolism*

Substances

  • CRTC2 protein, human
  • NF-kappa B
  • Transcription Factors
  • epidermal growth factor receptor VIII
  • ErbB Receptors