Primary biliary cholangitis: A tale of epigenetically-induced secretory failure?

J Hepatol. 2018 Dec;69(6):1371-1383. doi: 10.1016/j.jhep.2018.08.020. Epub 2018 Sep 5.

Abstract

Primary biliary cholangitis (PBC) is a chronic cholestatic liver disease associated with autoimmune-related destruction of small to medium size intrahepatic bile ducts. The aetiology of PBC is unknown and its pathogenesis remains obscure. Both genetic variants and environmental factors have been linked to increased PBC susceptibility, with other alterations known to cooperate in disease pathobiology. Increasing evidence indicates the presence of epigenetic abnormalities in PBC, particularly alterations of cholangiocellular microRNAs (miRNAs or miRs). This review highlights and discusses the most relevant epigenetic alterations found in patients with PBC, focusing on the role of miR-506 in the promotion of cholestasis and immune activation.

Keywords: AE2; Biliary bicarbonate; Cholangiocytes; PBC; miR-506.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Autoantibodies
  • Biomarkers / metabolism
  • Chloride-Bicarbonate Antiporters / metabolism*
  • Cholestasis / metabolism
  • DNA Methylation
  • Dihydrolipoyllysine-Residue Acetyltransferase / immunology
  • Epigenesis, Genetic*
  • Genetic Predisposition to Disease
  • Humans
  • Liver Cirrhosis, Biliary / genetics*
  • Liver Cirrhosis, Biliary / immunology
  • Liver Cirrhosis, Biliary / metabolism*
  • MicroRNAs / genetics*
  • MicroRNAs / metabolism
  • Polymorphism, Single Nucleotide
  • RNA, Long Noncoding / genetics
  • RNA, Long Noncoding / immunology

Substances

  • Autoantibodies
  • Biomarkers
  • Chloride-Bicarbonate Antiporters
  • MicroRNAs
  • RNA, Long Noncoding
  • Dihydrolipoyllysine-Residue Acetyltransferase