Obesity-related hepatocellular carcinoma: roles of risk factors altered in obesity

Front Biosci (Landmark Ed). 2012 Jun 1;17(6):2356-70. doi: 10.2741/4057.

Abstract

Epidemiological data have demonstrated that the prevalence of either obesity or hepatocellular carcinoma (HCC) is increasing worldwide during past decades, and obesity has been unequivocally shown to be a risk factor for HCC. It has been reported that a significant proportion of HCC in obesity develops in cryptogenic cirrhosis, which is largely associated with the progression of nonalcoholic fatty liver disease, especially nonalcoholic steatohepatitis. Since the HCC is a highly malignant tumor with a poor prognosis, a better understanding of the molecular mechanisms may help researchers to explore new approaches for preventing and treating the obesity-related HCC, and thereby facilitating a substantial reduction of morbidity and mortality. In this article, we reviewed the mechanisms underlying the relationship between obesity and HCC, with an emphasis on the roles of insulin/insulin-like growth factor axis, adipose tissue derived hormones, oxidative stress, and liver stem cells. In addition, we will discuss the impact of life-style modification on obesity-related HCC.

Publication types

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

MeSH terms

  • Adipokines / physiology
  • Adiponectin / physiology
  • Animals
  • Carcinoma, Hepatocellular / etiology*
  • Carcinoma, Hepatocellular / pathology
  • Carcinoma, Hepatocellular / physiopathology
  • Carcinoma, Hepatocellular / prevention & control
  • Growth Substances / physiology
  • Humans
  • Insulin / physiology
  • Insulin Resistance / physiology
  • Leptin / physiology
  • Life Style
  • Liver Neoplasms / etiology*
  • Liver Neoplasms / pathology
  • Liver Neoplasms / physiopathology
  • Liver Neoplasms / prevention & control
  • Models, Biological
  • Obesity / complications*
  • Obesity / pathology
  • Obesity / physiopathology
  • Oxidative Stress
  • Risk Factors
  • Signal Transduction
  • Somatomedins / physiology
  • Stem Cells / pathology
  • Stem Cells / physiology

Substances

  • ADIPOQ protein, human
  • Adipokines
  • Adiponectin
  • Growth Substances
  • Insulin
  • Leptin
  • Somatomedins