Constitutional and functional genetics of human alcohol-related hepatocellular carcinoma

被引:14
|
作者
Nahon, Pierre [1 ,2 ,3 ]
Nault, Jean-Charles [1 ,2 ,3 ]
机构
[1] Hop Jean Verdier, AP HP, Serv Hepatol, Bondy, France
[2] Univ Paris 13, Bobigny, France
[3] Univ Paris 13, Univ Paris Descartes,Labex Oncoimmunol, Univ Paris Diderot,Equipe Labellisee Ligue Canc, Inserm,UMR Funct Genet Solid Tumours 1162, Paris, France
关键词
alcoholic liver disease; cirrhosis; genetics; liver cancer; single nucleotide polymorphisms; FATTY LIVER-DISEASE; GREATER-THAN-G; HEPATIC STELLATE CELLS; GROWTH-FACTOR GENE; PNPLA3; RS738409; SUPEROXIDE-DISMUTASE; CONFERS SUSCEPTIBILITY; FIBROSIS PROGRESSION; COMMON POLYMORPHISM; WIDE ASSOCIATION;
D O I
10.1111/liv.13419
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Exploration of the constitutional genetics of hepatocellular carcinoma (HCC) has identified numerous variants associated with a higher risk of liver cancer in alcoholic cirrhotic patients. Although Genome-Wide Association studies have not been carried out in the field of alcohol-related HCC, common single nucleotide polymorphisms conferring a small increase in the risk of liver cancer risk have been identified and shown to modulate ethanol metabolism, inflammation, oxidative stress, iron or lipid metabolism. Specific patterns of gene mutations including CTNNB1, TERT, ARID1A and SMARCA2 exist in alcohol-related HCC. Moreover, a specific mutational process observed at the nucleotide level by next generation sequencing has revealed cooperation between alcohol and tobacco in the development of HCC. Combining this genetic information with epidemiological and clinical data that might define specific HCC risk classes and refine surveillance strategies needs to be assessed in large prospective cohorts of patients with alcoholic cirrhosis.
引用
收藏
页码:1591 / 1601
页数:11
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