4.3 Review

Genetics of Hepatobiliary Carcinogenesis

期刊

SEMINARS IN LIVER DISEASE
卷 31, 期 2, 页码 173-187

出版社

THIEME MEDICAL PUBL INC
DOI: 10.1055/s-0031-1276646

关键词

Hepatocellular carcinoma; genetic alterations; P53; beta-catenin; target therapy

资金

  1. ARC [3194]
  2. BioIntelligence (OSEO)
  3. Inca (PAIR-HCC NoFLIC'')

向作者/读者索取更多资源

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.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.3
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据