Molecular alterations in hepatocarcinogenesis induced by dietary methyl deficiency

Mol Nutr Food Res. 2012 Jan;56(1):116-25. doi: 10.1002/mnfr.201100524. Epub 2011 Nov 17.

Abstract

A chronic deficiency of major dietary methyl group donors--methionine, choline, folic acid, and vitamin B12--can induce the development of liver cancer in rodents. Feeding methyl-deficient diets causes several molecular alterations, including altered lipid metabolism, oxidative stress, deregulated one-carbon metabolism, and a number of epigenetic abnormalities that result in progressive liver injury culminating in the development of primary liver tumors. Importantly, this methyl-deficient model of endogenous hepatocarcinogenesis is one of the most relevant models of human liver carcinogenesis that allows studying liver cancer pathogenesis by substantially complementing many shortcomings of humans-only studies. In this review, we describe molecular changes and their role in pathogenesis of liver carcinogenesis induced by methyl deficiency.

Publication types

  • Review

MeSH terms

  • Animals
  • DNA Damage
  • DNA Methylation
  • Deficiency Diseases / complications*
  • Deficiency Diseases / metabolism*
  • Diet
  • Epigenesis, Genetic
  • Histones / metabolism
  • Humans
  • Lipid Metabolism
  • Liver Neoplasms / etiology*
  • Methionine / deficiency
  • Methionine / metabolism
  • MicroRNAs / metabolism
  • Oxidative Stress

Substances

  • Histones
  • MicroRNAs
  • Methionine