The oncogene phosphatidylinositol 3′-kinase catalytic subunit α promotes angiogenesis via vascular endothelial growth factor in ovarian carcinoma

Lin Zhang, Nuo Yang, Dionyssios Katsaros, Wei Huang, Jin Wan Park, Stefano Fracchioli, Cristina Vezzani, Irene A.Rigault De la Longrais, Weijia Yao, Stephen C. Rubin, George Coukos

Research output: Contribution to journalArticlepeer-review

68 Scopus citations

Abstract

The gene of phosphatidylinositol 3-kinase catalytic subunit α (PIK3CA) has been implicated as an oncogene in ovarian cancer [L. Shayesteh et al., Nat. Genet., 21: 99-102, 1999]. In this study, we examined the expression of PIK3CA mRNA and its p110α protein product in human ovarian carcinoma and investigated its role in regulating angiogenesis via vascular endothelial growth factor (VEGF). PIK3CA mRNA was detected in 66.6% of stage I and 93.9% of advanced stage ovarian cancer specimens and in all 17 ovarian cancer cell lines. PIK3CA mRNA levels were significantly higher in invasive carcinomas compared with benign and low malignant potential neoplasms (P = 0.007), but no significant difference was seen between early and advanced stage carcinomas (P = 0.812). Strong expression of immunoreactive p110α was detected in tumor cells and/or stroma endothelium. PIK3CA expression in vivo positively correlated, both at the mRNA and the protein level, with the expression of VEGF as well as with the extent of microvascular development. Furthermore, PIK3CA mRNA overexpression positively correlated with increased proliferation and decreased apoptosis of tumor cells in vivo. In vitro, PIK3CA expression positively correlated with the expression of VEGF in ovarian cancer cells, whereas the phosphatidylinositol 3′-kinase inhibitor Ly294002 reduced both the constitutive and inducible expression of hypoxia-inducible factor-1α at the mRNA and protein levels and abrogated VEGF up-regulation by glucose starvation. Furthermore, Ly294002 suppressed cell proliferation and, at higher doses, induced marked apoptosis in ovarian cancer cells. Collectively, these data strongly indicate that PIK3CA supports ovarian cancer growth through multiple and independent pathways affecting cell proliferation, apoptosis and angiogenesis, and plays an important role in ovarian cancer progression.

Original languageEnglish
Pages (from-to)4225-4231
Number of pages7
JournalCancer Research
Volume63
Issue number14
StatePublished - Jul 15 2003

Keywords

  • Apoptosis/physiology
  • Catalytic Domain
  • Cell Division/physiology
  • Chromones/pharmacology
  • Endothelial Growth Factors/biosynthesis
  • Enzyme Inhibitors/pharmacology
  • Female
  • Gene Expression Regulation, Enzymologic
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Intercellular Signaling Peptides and Proteins/biosynthesis
  • Lymphokines/biosynthesis
  • Morpholines/pharmacology
  • Neovascularization, Pathologic/enzymology
  • Ovarian Neoplasms/blood supply
  • Phosphatidylinositol 3-Kinases/biosynthesis
  • Phosphoinositide-3 Kinase Inhibitors
  • RNA, Messenger/biosynthesis
  • Transcription Factors/metabolism
  • Vascular Endothelial Growth Factor A
  • Vascular Endothelial Growth Factors

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