Overexpression of PDGFA and its receptor during carcinogenesis of Opisthorchis viverrini-associated cholangiocarcinoma

Parasitol Int. 2012 Mar;61(1):145-50. doi: 10.1016/j.parint.2011.07.008. Epub 2011 Jul 14.

Abstract

Cholangiocarcinoma (CCA) is a crucial health problem in northeastern part of Thailand, which is caused by a combination of Opisthorchis viverrini infection and nitrosamine. A better understanding of its molecular mechanism is an important step to discover and develop the new diagnostics and therapies for CCA. To reveal the involvement of potential genes in the development of CCA, the present study investigated the expression kinetics of platelet-derived growth factor alpha (Pdgfa) and its receptor (Pdgfra) during the tumorigenesis of CCA induced by O. viverrini infection with quantitative RT-PCR, and confirmed the expression with immunohistological staining. The results showed that in the hamster model of opisthorchiasis-associated CCA, the expression of Pdgfa was increased after infection plus N-nitrosodimethylamine (NDMA) administration, reached its peak at 2 months post infection, and remained at the high level until 6 months. Similarly, the expression of Pdgfra was increased time-dependently. The positive immunostaining for PDGFA proteins was observed in the cytoplasm of epithelial tumor cells of hamster CCA. Moreover, the analysis of the expression of these genes in 10 cases of human opisthorchiasis-associated CCA showed that Pdgfa was overexpressed in 80%, and Pdgfra was overexpressed in 40% cases (>3.0 folds, compared with the expressions of adjacent normal tissues). This result suggests that PDGFA is likely involved in the tumorigenesis of opisthorchiasis-associated CCA, and may be a promising candidate biomarker for diagnosis and treatment strategies of CCA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bile Duct Neoplasms / chemically induced
  • Bile Duct Neoplasms / genetics*
  • Bile Duct Neoplasms / metabolism
  • Bile Duct Neoplasms / parasitology
  • Bile Ducts, Intrahepatic / metabolism
  • Bile Ducts, Intrahepatic / parasitology
  • Bile Ducts, Intrahepatic / pathology
  • Cell Transformation, Neoplastic / chemically induced
  • Cell Transformation, Neoplastic / genetics
  • Cell Transformation, Neoplastic / pathology
  • Cholangiocarcinoma / chemically induced
  • Cholangiocarcinoma / genetics*
  • Cholangiocarcinoma / parasitology
  • Cholangiocarcinoma / pathology
  • Cricetinae
  • Dimethylnitrosamine
  • Disease Models, Animal
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Immunohistochemistry
  • Male
  • Mesocricetus
  • Opisthorchiasis / complications*
  • Opisthorchiasis / parasitology
  • Opisthorchiasis / physiopathology
  • Opisthorchis / physiology
  • Platelet-Derived Growth Factor / metabolism
  • Real-Time Polymerase Chain Reaction
  • Receptor, Platelet-Derived Growth Factor alpha / metabolism*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Rodent Diseases / chemically induced
  • Rodent Diseases / parasitology
  • Rodent Diseases / physiopathology
  • Thailand

Substances

  • Platelet-Derived Growth Factor
  • platelet-derived growth factor A
  • Receptor, Platelet-Derived Growth Factor alpha
  • Dimethylnitrosamine