1. Hepatocellular carcinoma in the setting of alcohol-related liver disease 
Nathalie Ganne-Carrié, Pierre Nahon 
Journal of Hepatology 
Volume 70, Issue 2, Pages (February 2019)
DOI: /j.jhep
Copyright © 2018 European Association for the Study of the Liver Terms and Conditions

2. Fig. 1
Geographical distribution of the contribution of alcohol to absolute primary liver cancer deaths in Europe for both genders (adapted from Akinyemiju T et al. JAMA Oncol 2017;3:1683–1691, Table S10e).
Journal of Hepatology  , DOI: ( /j.jhep )
Copyright © 2018 European Association for the Study of the Liver Terms and Conditions

3. Fig. 2
Biological pathways involved in alcohol-mediated liver carcinogenesis. Ethanol is first metabolised by alcohol dehydrogenase (ADH) into carcinogenic acetaldehyde, which causes major cell damage by forming DNA and protein adducts. CYP2E1 also triggers the formation of acetaldehyde and reactive oxygen species (ROS). Oxidative stress secondary to ROS accumulation damages cell components through lipid peroxidation and DNA mutagenesis via the formation of adducts and the impairment of repair mechanisms. The effects of iron and lipid accumulation usually observed in ALD also participate in ROS accumulation, and further aggravate the deleterious effects of oxidative stress. In addition, alcohol promotes inflammation via the translocation of gut bacteria and lipopolysaccharide, which trigger the production of pro-inflammatory cytokines and chemokines implicated in both the anti-tumour immune response and ROS formation. Acetaldehyde also alters methyl transfer, leading to DNA hypomethylation associated with modifications to gene expression (oncogenes and tumour suppressor genes). The principal variants reported as being potential genetic modifiers of the liver cancer risk in patients with ALD are depicted as a function of their specific interactions with these molecular pathways.
Journal of Hepatology  , DOI: ( /j.jhep )
Copyright © 2018 European Association for the Study of the Liver Terms and Conditions