β4 and β6 Integrin Expression Is Associated with the Subclassification and Clinicopathological Features of Intrahepatic Cholangiocarcinoma

Int J Mol Sci. 2018 Mar 27;19(4):1004. doi: 10.3390/ijms19041004.

Abstract

Intrahepatic cholangiocarcinoma (ICC) is a heterogeneous group of cancers of the intrahepatic biliary tract. However, few studies have evaluated integrin expression according to an ICC subgroup. We immunohistochemically investigated α6β4 (β4) and αvβ6 (β6) integrin expressions in 48 ICCs, and evaluated their relationship with clinical and pathological parameters and ligand expression, as well as transforming growth factor (TGF)-β1. β4 and β6 expressions were detected in 46 (96%) and 35 (73%) ICC cases, respectively. We classified ICC into negative, low (β4, 29 cases; β6, 36 cases), or high (β4, 19 cases; β6, 12 cases) integrin expression groups. β4 and β6 integrin levels were higher in the non-peripheral central localization type ICC than in the peripheral localization type; they were also higher in the periductal-infiltrating or intraductal-growth types than in the mass-forming type ICC; lastly, they were higher in the well-differentiated type than in the poorly-differentiated type ICC. High expression was related to bile duct invasion. In addition, β4 and β6 expressions were associated with mucin production and the expression of cytoplasmic epithelial membrane antigen, laminin-5, and tenascin-C. TGF-β1 was correlated with β6 expression and poor overall survival. These results suggest that integrin expression is associated with subclassification and clinicopathological features of ICC through the coincident expression of their ligands and TGF-β1.

Keywords: TGF-β1; classifications; integrin; intrahepatic cholangiocarcinoma; laminin; tenascin.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Antigens, Neoplasm / metabolism*
  • Bile Duct Neoplasms / classification
  • Bile Duct Neoplasms / metabolism
  • Bile Duct Neoplasms / pathology*
  • Cholangiocarcinoma / classification
  • Cholangiocarcinoma / metabolism
  • Cholangiocarcinoma / pathology*
  • Cytoplasm / metabolism
  • Down-Regulation*
  • Female
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Integrin alpha6beta4 / metabolism*
  • Integrins / metabolism*
  • Male
  • Middle Aged
  • Mucins / metabolism
  • Transforming Growth Factor beta1 / metabolism

Substances

  • Antigens, Neoplasm
  • Integrin alpha6beta4
  • Integrins
  • Mucins
  • TGFB1 protein, human
  • Transforming Growth Factor beta1
  • integrin alphavbeta6