Insulin receptor substrate-2 mediated insulin-like growth factor-I receptor overexpression in pancreatic adenocarcinoma through protein kinase Cdelta

Cancer Res. 2009 Feb 15;69(4):1350-7. doi: 10.1158/0008-5472.CAN-08-1328. Epub 2009 Feb 3.

Abstract

Pancreatic adenocarcinoma (PCA) is an almost invariably fatal disease. Recently, it has been shown by several groups as well as ours that insulin-like growth factor-I receptor (IGF-IR) overexpression is related to higher proliferation, survival, angiogenesis, and highly invasive pancreatic tumors. Several studies have been carried out to understand the pathways that lead to growth factor-mediated signaling, but the molecular mechanism of receptor overexpression remains mostly unknown. Treatment with neutralizing antibodies or a specific kinase inhibitor against IGF-IR could block the receptor expression in PCA cells. Furthermore, we also showed that insulin receptor substrate (IRS)-2, but not IRS-1, is involved in regulation of IGF-IR expression, which is most likely not transcriptional control. By blocking mammalian target of rapamycin (mTOR) pathway with rapamycin as well as other biochemical analysis, we defined a unique regulation of IGF-IR expression mediated by protein kinase Cdelta (PKCdelta) and mTOR pathway. Moreover, we showed that the down-regulation of IGF-IR expression due to IRS-2 small interfering RNA can be compensated by overexpression of dominant-active mutant of PKCdelta, suggesting that PKCdelta is downstream of IGF-IR/IRS-2 axis. Overall, these findings suggest a novel regulatory role of IRS-2 on the expression of IGF-IR through PKCdelta and mTOR in pancreatic cancer cells.

Publication types

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

MeSH terms

  • Adenocarcinoma / enzymology
  • Adenocarcinoma / genetics*
  • Adenocarcinoma / physiopathology
  • Cell Division
  • Cell Line, Tumor
  • DNA Primers
  • Gene Expression Regulation, Enzymologic
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Insulin Receptor Substrate Proteins / physiology*
  • Neoplasm Invasiveness
  • Neovascularization, Pathologic
  • Pancreatic Neoplasms / enzymology
  • Pancreatic Neoplasms / genetics*
  • Pancreatic Neoplasms / physiopathology
  • Polymerase Chain Reaction
  • Protein Biosynthesis
  • Protein Kinase C-delta / genetics*
  • Protein Kinase C-delta / metabolism
  • Protein Kinases / physiology
  • RNA, Neoplasm / genetics
  • RNA, Small Interfering / genetics
  • Receptor, IGF Type 1 / genetics*
  • TOR Serine-Threonine Kinases

Substances

  • DNA Primers
  • IRS1 protein, human
  • IRS2 protein, human
  • Insulin Receptor Substrate Proteins
  • RNA, Neoplasm
  • RNA, Small Interfering
  • Protein Kinases
  • MTOR protein, human
  • Receptor, IGF Type 1
  • TOR Serine-Threonine Kinases
  • Protein Kinase C-delta