Genetics of Hepatobiliary Carcinogenesis

被引:135
作者
Nault, Jean-Charles [1 ,2 ]
Zucman-Rossi, Jessica [1 ,2 ,3 ]
机构
[1] INSERM, U674, F-75010 Paris, France
[2] Univ Paris 05, Fac Med, Paris, France
[3] HEGP, AP HP, Dept Oncol, Paris, France
关键词
Hepatocellular carcinoma; genetic alterations; P53; beta-catenin; target therapy; GROWTH-FACTOR-RECEPTOR; TUMOR-SUPPRESSOR GENE; PRIMARY SCLEROSING CHOLANGITIS; BETA-CATENIN MUTATIONS; HEPATITIS-B-VIRUS; HUMAN HEPATOCELLULAR CARCINOMAS; FOCAL NODULAR HYPERPLASIA; PIK3CA HOTSPOT MUTATIONS; BILIARY-TRACT CARCINOMA; K-RAS MUTATIONS;
D O I
10.1055/s-0031-1276646
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Hepatocellular carcinoma (HCC) and cholangiocarcinoma (CC) are two leading causes of cancer death in the world. Liver carcinogenesis is driven by genetic alterations in combination with viral and environmental factors. beta-catenin and P53 mutations represent the two main genetic alterations described in HCC, and P53 and KRAS mutations in CC, but rare genetic alterations could be particularly valuable if they constitute drug-able targets (such as PIK3CA or EGFR mutations). Recent progress using global genomic analysis has highlighted the marked genetic heterogeneity of this disease and this approach has also been used to assess prognosis or refine the diagnosis. The validation of sorafenib as the first targeted therapy useful in HCC has opened up new prospects for biotherapy in this cancer. In the future, mapping of genetic alterations will be essential to adapt treatment to HCC and CC biology.
引用
收藏
页码:173 / 187
页数:15
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