Signaling pathways regulating TC21-induced tumorigenesis

J Biol Chem. 2007 Sep 21;282(38):27713-20. doi: 10.1074/jbc.M703037200. Epub 2007 Jul 26.

Abstract

TC21(R-Ras2), a Ras-related GTPase with transforming potential similar to H-, K- and N-Ras, is implicated in the pathogenesis of human cancers. Transforming growth factor beta (TGF-beta), a cytokine that plays a significant role in modulating tumorigenesis, normally prevents uncontrolled cell proliferation but paradoxically induces proliferation in H-Ras-transformed cancer cells. Although TC21 activates some pathways that mediate cellular transformation by the classical Ras proteins, the mechanisms through which TC21 induces tumor formation and how TGF-beta regulates TC21 transformed cells is not known. To better understand the role of TC21 in cancer progression, we overexpressed an activated G23V mutant of TC21 in a nontumorigenic murine mammary epithelial (EpH4) cell line. Mutant TC21-expressing cells were significantly more oncogenic than cells expressing activated G12V H-Ras both in vivo and in vitro. TC21-induced transformation and proliferation required activation of p38 MAPK, mTOR (the mammalian target of rapamycin), and phosphoinositide 3-kinase but not Akt/PKB. Transformation by TC21 rendered EpH4 cells insensitive to the growth inhibitory effects of TGF-beta, and the soft agar growth of these cells was increased upon TGF-beta stimulation. Despite losing responsiveness to TGF-beta-mediated growth inhibition, both Smad-dependent and independent pathways remained intact in TC21-transformed cells. Thus, overexpression of active TC21 in EpH4 cells induces tumorigenicity through the phosphoinositide 3-kinase, p38 MAPK, and mTOR pathways, and these cells lose their sensitivity to the normal growth inhibitory role of TGF-beta.

Publication types

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

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Female
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • MAP Kinase Signaling System
  • Membrane Proteins / physiology*
  • Mice
  • Mice, Inbred BALB C
  • Monomeric GTP-Binding Proteins / physiology*
  • Protein Kinases / metabolism
  • Signal Transduction*
  • TOR Serine-Threonine Kinases
  • Transforming Growth Factor beta / metabolism
  • p38 Mitogen-Activated Protein Kinases / metabolism
  • ras Proteins / metabolism

Substances

  • Membrane Proteins
  • Transforming Growth Factor beta
  • Protein Kinases
  • MTOR protein, human
  • mTOR protein, mouse
  • TOR Serine-Threonine Kinases
  • p38 Mitogen-Activated Protein Kinases
  • RRAS2 protein, human
  • Rras2 protein, mouse
  • Monomeric GTP-Binding Proteins
  • ras Proteins