4.8 Article

The Cancer Genome Atlas Comprehensive Molecular Characterization of Renal Cell Carcinoma

期刊

CELL REPORTS
卷 23, 期 1, 页码 313-+

出版社

CELL PRESS
DOI: 10.1016/j.celrep.2018.03.075

关键词

-

资金

  1. NIH Genome sequencing center [U54 HG003273, U54 HG003067, U54 HG003079]
  2. NIH Genome data analysis center and genome characterization center [U24 CA143799, U24 CA143835, U24 CA143840, U24 CA143843, U24 CA143845, U24 CA143848, U24 CA143858, U24 CA143866, U24 CA143867, U24 CA143882, U24 CA143883, U24 CA144025]
  3. NIH PCC grant [P30 CA016672]
  4. Frederick National Laboratory for Cancer Research, NIH [HHSN261200800001E]

向作者/读者索取更多资源

Renal cell carcinoma(RCC) is not a single disease, but several histologically defined cancers with different genetic drivers, clinical courses, and therapeutic responses. The current study evaluated 843 RCC from the three major histologic subtypes, including 488 clear cell RCC, 274 papillary RCC, and 81 chromophobe RCC. Comprehensive genomic and phenotypic analysis of the RCC subtypes reveals distinctive features of each subtype that provide the foundation for the development of subtype-specific therapeutic and management strategies for patients affected with these cancers. Somatic alteration of BAP1, PBRM1, and PTEN and altered metabolic pathways correlated with subtype-specific decreased survival, while CDKN2A alteration, increased DNA hypermethylation, and increases in the immune-related Th2 gene expression signature correlated with decreased survival within all major histologic subtypes. CIMP-RCC demonstrated an increased immune signature, and a uniform and distinct metabolic expression pattern identified a subset of metabolically divergent (MD) ChRCC that associated with extremely poor survival.

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

4.8
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