Expression of DPC4/Smad4 gene in stone-containing intrahepatic bile duct

J Surg Oncol. 2006 Sep 15;94(4):338-43. doi: 10.1002/jso.20517.

Abstract

Background and objectives: Hepatolithiasis is etiologically related to cholangiocarcinoma. We underwent this study with an attempt to examine the expression of DPC4/Smad4 gene in stone-containing intrahepatic bile ducts (IHD) and intrahepatic cholangiocarcinoma (ICC).

Patients and methods: The immunohistochemical method and RT-PCR analysis were used to study the expression of DPC4/Smad4 gene in normal IHD, stone-containing IHD, and ICC. All the specimens were from hepatic resection.

Results: The immunohistochemical study showed that all specimens from 24 normal IHD had marked expression of DPC4/Smad4 gene, while there was 4.4% (2/46) and 33.3% (3/9) loss of DPC4/Smad4 expression in stone-containing IHD and ICC, respectively. Among the specimens of stone-containing IHD, all the hyperplastic epithelial cells showed normal expression of DPC4/Smad4 gene while dysplastic epithelial cells showed 20% (2/10) loss expression of DPC4/Smad4. The RT-PCR analysis showed that the normal IHD had the highest content of DPC4/Smad4 mRNA, which was threefold and sixfold higher than that of stone-containing IHD and ICC, respectively.

Conclusion: Loss expression of DPC4/Smad4 gene was found both in stone-containing IHD and ICC. Dysplastic epithelium of stone-containing IHD had higher potential for malignant transformation.

MeSH terms

  • Adult
  • Aged
  • Bile Duct Neoplasms / complications
  • Bile Duct Neoplasms / genetics*
  • Bile Duct Neoplasms / metabolism
  • Bile Ducts, Intrahepatic / chemistry*
  • Calculi / etiology*
  • Cholangiocarcinoma / complications
  • Cholangiocarcinoma / genetics*
  • Cholangiocarcinoma / metabolism
  • Female
  • Gallstones / complications
  • Humans
  • Immunohistochemistry
  • Liver Diseases / etiology*
  • Male
  • Middle Aged
  • RNA, Messenger / biosynthesis
  • Reverse Transcriptase Polymerase Chain Reaction
  • Smad4 Protein / biosynthesis*
  • Smad4 Protein / genetics*

Substances

  • RNA, Messenger
  • SMAD4 protein, human
  • Smad4 Protein