4.7 Article Proceedings Paper

Identification of the genes for kidney cancer: Opportunity for disease-specific targeted therapeutics

期刊

CLINICAL CANCER RESEARCH
卷 13, 期 2, 页码 671S-679S

出版社

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/1078-0432.CCR-06-1870

关键词

-

类别

资金

  1. Intramural NIH HHS Funding Source: Medline
  2. NCI NIH HHS [N01 CO 12400] Funding Source: Medline

向作者/读者索取更多资源

Recent advances in understanding the kidney cancer gene pathways has provided the foundation for the development of targeted therapeutic approaches for patients with this disease. Kidney cancer is not a single disease; it includes a number of different types of renal cancers, each with different histologic features, a different clinical course, a different response to therapy, and different genes causing the defects. Most of what is known about the genetic basis of kidney cancer has been learned from study of the inherited forms of kidney cancer: von Hippel Lindau (VHL gene), hereditary papillary renal carcinoma (c-Met gene), Birt Hogg Dube (BHD gene), and hereditary leiomyomatosis renal cell cancer (fumarate hydratase gene). These Mendelian single-gene syndromes provide a unique opportunity to evaluate the effectiveness of agents that target the VHL, c-Met, BHD, and fumarate hydratase pathways.

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

4.7
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