Relationship between interleukin-6 and proliferation and differentiation in cholangiocarcinoma

Histopathology. 1998 Aug;33(2):145-53. doi: 10.1046/j.1365-2559.1998.00445.x.

Abstract

Aims: Interleukin-6 (IL-6) has been implicated as a mediator of growth control in several human neoplasms. The significance of IL-6 expression in human cholangiocarcinoma was examined in this study.

Methods and results: IL-6 expression was examined in 43 surgically resected cholangiocarcinomas and a cholangiocarcinoma cell line CCKS1, derived from abdominal metastasis of moderately differentiated adenocarcinoma, by immunohistochemical and in-situ hybridization techniques. In non-neoplastic bile ducts, IL-6 was constitutively but weakly expressed. In surgical cases of cholangiocarcinoma, IL-6 was frequently and strongly expressed in the cytoplasm of well-differentiated cholangiocarcinoma, while its expression was decreased, and less intense or absent in moderately and poorly differentiated areas, respectively. IL-6 mRNA was detected in the cytoplasm of carcinoma cells of two cases of cholangiocarcinomas positive for IL-6. IL-6 was detected in hepatic bile from two cholangiocarcinoma cases studied. The proliferation antigen Ki67 was found to be more frequently expressed in IL-6 negative carcinoma cells than in IL-6 positive carcinoma cells (P < 0.01). In cultured carcinoma cells line CCKS1, IL-6, IL-6 mRNA and IL-6 receptor alpha chain were detected in the cytoplasm of carcinoma cells, suggesting an autocrine effect of IL-6 on carcinoma cells.

Conclusion: IL-6 expression is inversely related to cell proliferation and positively related to differentiation in cholangiocarcinoma.

MeSH terms

  • Aged
  • Animals
  • Bile / immunology
  • Bile Duct Neoplasms / immunology*
  • Bile Duct Neoplasms / pathology
  • Bile Ducts, Intrahepatic*
  • Blotting, Western
  • Cell Differentiation
  • Cell Division
  • Cholangiocarcinoma / immunology*
  • Cholangiocarcinoma / pathology*
  • Female
  • Humans
  • Immunohistochemistry
  • In Situ Hybridization
  • Interleukin-6 / metabolism*
  • Ki-67 Antigen / metabolism
  • Male
  • Mice
  • Mice, Nude
  • Middle Aged
  • Neoplasm Transplantation
  • RNA, Messenger / analysis
  • Tumor Cells, Cultured

Substances

  • Interleukin-6
  • Ki-67 Antigen
  • RNA, Messenger