Oncogenic transformation induced by the p110beta, -gamma, and -delta isoforms of class I phosphoinositide 3-kinase

Proc Natl Acad Sci U S A. 2006 Jan 31;103(5):1289-94. doi: 10.1073/pnas.0510772103. Epub 2006 Jan 23.

Abstract

Class I phosphoinositide 3-kinase contains four isoforms of the catalytic subunit, p110alpha, -beta, -gamma, and -delta. At physiological levels of expression, the wild-type p110alpha isoform lacks oncogenic potential, but gain-of-function mutations and overexpression of p110alpha are correlated with oncogenicity. The p110beta, -gamma, and -delta isoforms induce transformation of cultured cells as wild-type proteins. This oncogenic potential requires kinase activity and can be suppressed by the target of rapamycin inhibitor rapamycin. The p110delta isoform constitutively activates the Akt signaling pathway; p110gamma activates Akt only in the presence of serum. The isoforms differ in their requirements for upstream signaling. The transforming activity of the p110gamma isoform depends on rat sarcoma viral oncogene homolog (Ras) binding; preliminary data suggest the same for p110beta and indicate Ras-independent oncogenic potential of p110delta. The surprising oncogenic potential of the wild-type non-alpha isoforms of class I phosphoinositide 3-kinase may explain the dearth of cancer-specific mutations in these proteins, because these non-alpha isoforms could contribute to the oncogenic phenotype of the cell by differential expression.

Publication types

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

MeSH terms

  • Animals
  • Antibiotics, Antineoplastic / pharmacology
  • Blotting, Western
  • Cell Differentiation
  • Cell Line, Tumor
  • Cell Transformation, Neoplastic*
  • Cells, Cultured
  • Chick Embryo
  • Class I Phosphatidylinositol 3-Kinases
  • Culture Media, Serum-Free / pharmacology
  • Humans
  • Mutagenesis, Site-Directed
  • Mutation
  • Phosphatidylinositol 3-Kinases / chemistry*
  • Phosphatidylinositol 3-Kinases / metabolism
  • Plasmids / metabolism
  • Point Mutation
  • Protein Binding
  • Protein Isoforms
  • Protein Kinases / metabolism
  • Signal Transduction
  • Sirolimus / pharmacology
  • TOR Serine-Threonine Kinases
  • Time Factors
  • Transfection
  • ras Proteins / metabolism

Substances

  • Antibiotics, Antineoplastic
  • Culture Media, Serum-Free
  • Protein Isoforms
  • Protein Kinases
  • MTOR protein, human
  • mTOR protein, rat
  • Class I Phosphatidylinositol 3-Kinases
  • PIK3CB protein, human
  • TOR Serine-Threonine Kinases
  • ras Proteins
  • Sirolimus