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The Cancer Genome Atlas Comprehensive Molecular Characterization of Renal Cell Carcinoma.

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BORIS DOI
10.7892/boris.126379
Date of Publication
April 3, 2018
Publication Type
Article
Author
Ricketts, Christopher J
De Cubas, Aguirre A
Fan, Huihui
Smith, Christof C
Lang, Martin
Reznik, Ed
Bowlby, Reanne
Gibb, Ewan A
Akbani, Rehan
Beroukhim, Rameen
Bottaro, Donald P
Choueiri, Toni K
Gibbs, Richard A
Godwin, Andrew K
Haake, Scott
Hakimi, A Ari
Henske, Elizabeth P
Hsieh, James J
Ho, Thai H
Kanchi, Rupa S
Krishnan, Bhavani
Kwiatkowski, David J
Lui, Wembin
Merino, Maria J
Mills, Gordon B
Myers, Jerome
Nickerson, Michael L
Reuter, Victor E
Schmidt, Laura S
Shelley, C Simon
Shen, Hui
Shuch, Brian
Signoretti, Sabina
Srinivasan, Ramaprasad
Tamboli, Pheroze
Thomas, George
Vincent, Benjamin G
Vocke, Cathy D
Wheeler, David A
Yang, Lixing
Kim, William Y
Robertson, A Gordon
Spellman, Paul T
Rathmell, W Kimryn
Linehan, W Marston
Subject(s)

600 - Technology::610...

Series
Cell reports
ISSN or ISBN (if monograph)
2211-1247
Publisher
Cell Press
Language
English
Publisher DOI
10.1016/j.celrep.2018.03.075
PubMed ID
29617669
Uncontrolled Keywords

CDKN2A DNA hypermethy...

Description
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.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/64163
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FileFile TypeFormatSizeLicensePublisher/Copright statementContent
nihms958988.pdftextAdobe PDF1.63 MBAttribution (CC BY 4.0)acceptedOpen
1-s2.0-S2211124718304364-main.pdftextAdobe PDF6.55 MBAttribution (CC BY 4.0)publishedOpen
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