Ral GTPase down-regulation stabilizes and reactivates p53 to inhibit malignant transformation

J Biol Chem. 2014 Nov 7;289(45):31296-309. doi: 10.1074/jbc.M114.565796. Epub 2014 Sep 10.

Abstract

Ral GTPases are critical effectors of Ras, yet the molecular mechanism by which they induce malignant transformation is not well understood. In this study, we found the expression of K-Ras, RalB, and sometimes RalA, but not AKT1/2 and c-Raf, to be required for maintaining low levels of p53 in human cancer cells that harbor mutant K-Ras and wild-type p53. Down-regulation of K-Ras, RalB, and sometimes RalA increases p53 protein levels and results in a p53-dependent up-regulation of the expression of p21(WAF). K-Ras, RalA, and RalB depletion increases p53 stability as demonstrated by ataxia telangiectasia-mutated kinase activation, increased Ser-15 phosphorylation, and a significant (up to 6-fold) increase in p53 half-life. Furthermore, depletion of K-Ras and RalB inhibits anchorage-independent growth and invasion and interferes with cell cycle progression in a p53-dependent manner. Depletion of RalA inhibits invasion in a p53-dependent manner. Thus, expression of K-Ras and RalB and possibly RalA proteins is critical for maintaining low levels of p53, and down-regulation of these GTPases reactivates p53 by significantly enhancing its stability, and this contributes to suppression of malignant transformation.

Keywords: Apoptosis; Cancer Biology; K-Ras; RalA; RalB; Ras Protein; Serine 15 Phosphorylation; Signal Transduction; p53.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Caspases / metabolism
  • Cell Cycle
  • Cell Line, Tumor
  • Cell Transformation, Neoplastic*
  • Cyclin-Dependent Kinase Inhibitor p21 / metabolism*
  • Down-Regulation
  • Enzyme Activation
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • Phosphorylation
  • Proto-Oncogene Proteins p21(ras) / metabolism
  • RNA, Small Interfering / metabolism
  • Serine / chemistry
  • Signal Transduction
  • Tumor Suppressor Protein p53 / metabolism*
  • ral GTP-Binding Proteins / metabolism*

Substances

  • CDKN1A protein, human
  • Cyclin-Dependent Kinase Inhibitor p21
  • RNA, Small Interfering
  • Ralb protein, human
  • TP53 protein, human
  • Tumor Suppressor Protein p53
  • Serine
  • Caspases
  • RALA protein, human
  • Proto-Oncogene Proteins p21(ras)
  • ral GTP-Binding Proteins