Estrogens and the pathophysiology of the biliary tree

World J Gastroenterol. 2006 Jun 14;12(22):3537-45. doi: 10.3748/wjg.v12.i22.3537.

Abstract

The scientific framework concerning estrogen effects on different tissues has expanded enormously during the last decades, when estrogen receptor (ER) subtypes were identified. Estrogens are not only essential for the female reproductive system, but they also control fundamental functions in other tissues including the cardiovascular system, bone, brain and liver. Recently, estrogens have been shown to target the biliary tree, where they modulate the proliferative and secretory activities of cholangiocytes, the epithelial cells lining bile ducts. By acting on both estrogen receptors (ER-alpha) and (ER-beta) subtypes, and by activating either genomic or non-genomic pathways, estrogens play a key role in the complex loop of growth factors and cytokines, which modulates the proliferative response of cholangiocytes to damage. Specifically, estrogens activate intracellular signalling cascades [ERK(1/2) (extracellular regulated kinases (1/2), PI3- kinase/AKT (phosphatidylinositol-3' kinase/AKT)] typical of growth factors such as insulin like growth factor (IGF1), nerve growth factor (NGF) and vascular endothelial growth factor (VEGF), thus potentiating their action. In addition, estrogens stimulate the secretion of different growth factors in proliferating cholangiocytes. This review specifically deals with the recent advances related to the role and mechanisms by which estrogens modulate cholangiocyte functions in normal and pathological conditions.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Review

MeSH terms

  • Animals
  • Apoptosis / physiology
  • Bile Duct Neoplasms / pathology
  • Bile Duct Neoplasms / physiopathology
  • Bile Ducts, Intrahepatic / cytology*
  • Bile Ducts, Intrahepatic / physiopathology
  • Biliary Tract / pathology*
  • Biliary Tract / physiopathology*
  • Cell Proliferation
  • Cholangiocarcinoma / pathology
  • Cholangiocarcinoma / physiopathology
  • Cytokines / physiology
  • Endothelial Cells / drug effects
  • Endothelial Cells / physiology
  • Estrogens / physiology*
  • Growth Substances / physiology
  • Humans
  • Liver Cirrhosis, Biliary / pathology
  • Liver Cirrhosis, Biliary / physiopathology
  • Polycystic Kidney, Autosomal Dominant / pathology
  • Polycystic Kidney, Autosomal Dominant / physiopathology
  • Receptors, Estrogen / physiology*
  • Signal Transduction / physiology

Substances

  • Cytokines
  • Estrogens
  • Growth Substances
  • Receptors, Estrogen