Inhibin/activin expression in human and rodent liver: subunits α and βB as new players in human hepatocellular carcinoma?

Br J Cancer. 2011 Apr 12;104(8):1303-12. doi: 10.1038/bjc.2011.53. Epub 2011 Mar 15.

Abstract

Background: Activins and inhibins belong to the TGFβ-superfamily, which controls cell proliferation and differentiation in many organs. Activin A, the dimer of inhibin βA subunit, acts strongly anti-proliferative in hepatocytes. Little is known on the other activin/inhibin subunits in human liver and hepatocellular carcinoma (HCC).

Methods: We studied the expression of the complete inhibin family α, βA, βB, βC, βE in normal liver, tumour-adjacent and HCC tissue, 12 additional organs and rodent liver. A total of 16 HCC and 10 disease-free livers were analysed. Expression of inhibin subunits was determined by qRT-PCR, normalised to RNA input and by geNorm algorithm, and confirmed by immunohistochemistry.

Results: Remarkably, βA expression was not decreased in HCC. Similarly, βC and βE exhibited no major changes. In contrast, inhibin α, barely detectable in normal liver, was strongly increased in tumour-adjacent liver and dramatically enhanced in HCC. βB was strongly enhanced in some HCC. At variance with human liver, rodent liver showed higher inhibin α and βC expression, but βA was somewhat, and βB dramatically lower.

Conclusions: Upregulation of inhibin α - and possibly of βB - may shield HCC cells from anti-proliferative effects of activin A. Dramatic variations between humans and rodents may reflect different functions of some inhibins/activins.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Activins / genetics*
  • Activins / metabolism
  • Adult
  • Aged
  • Animals
  • Carcinoma, Hepatocellular / genetics*
  • Carcinoma, Hepatocellular / metabolism
  • Carcinoma, Hepatocellular / pathology
  • Case-Control Studies
  • Female
  • Gene Expression
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Inhibins / genetics*
  • Inhibins / metabolism
  • Liver / metabolism*
  • Liver Neoplasms / genetics*
  • Liver Neoplasms / metabolism
  • Liver Neoplasms / pathology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Middle Aged
  • Protein Subunits / genetics
  • Protein Subunits / metabolism
  • Rats
  • Rats, Wistar
  • Rodentia / genetics*
  • Rodentia / metabolism

Substances

  • Protein Subunits
  • Activins
  • Inhibins