NEJM. 374: 135-145, 04 November 2015 10.1056/NEJMoa1505917
Background: Papillary renal-cell carcinoma, which accounts for 15 to 20% of renal-cell carcinomas, is a heterogeneous disease that consists of various types of renal cancer, including tumors with indolent, multifocal presentation and solitary tumors with an aggressive, highly lethal phenotype. Little is known about the genetic basis of sporadic papillary renal-cell carcinoma, and no effective forms of therapy for advanced disease exist.
Methods: We performed comprehensive molecular characterization of 161 primary papillary renal-cell carcinomas, using whole-exome sequencing, copy-number analysis, messenger RNA and microRNA sequencing, DNA-methylation analysis, and proteomic analysis.
Results: Type 1 and type 2 papillary renal-cell carcinomas were shown to be different types of renal cancer characterized by specific genetic alterations, with type 2 further classified into three individual subgroups on the basis of molecular differences associated with patient survival. Type 1 tumors were associated with MET alterations, whereas type 2 tumors were characterized by CDKN2A silencing, SETD2 mutations, TFE3 fusions, and increased expression of the NRF2–antioxidant response element (ARE) pathway. A CpG island methylator phenotype (CIMP) was observed in a distinct subgroup of type 2 papillary renal-cell carcinomas that was characterized by poor survival and mutation of the gene encoding fumarate hydratase (FH).
Conclusions: Type 1 and type 2 papillary renal-cell carcinomas were shown to be clinically and biologically distinct. Alterations in the MET pathway were associated with type 1, and activation of the NRF2-ARE pathway was associated with type 2; CDKN2A loss and CIMP in type 2 conveyed a poor prognosis. Furthermore, type 2 papillary renal-cell carcinoma consisted of at least three subtypes based on molecular and phenotypic features. (Funded by the National Institutes of Health)
Data in the GDC
- GDC Manifests
- Open-Access Data - Download Manifest (18 Files)
- Controlled-Access Data - Download Manifest (3 Files)
Supplemental Data
These data represent a data freeze from Dec 7, 2014.
The data are supported by different organizations. All data marked by [Supplementary] were created by the manuscript authors and you should contact the corresponding author for support.
- Full KIRP Sample List:
- Clinical
- nationwidechildrens.org_KIRP.bio.Level_1[tar.gz] - XML files containing biospecimen processing and clinical data
- DNA Mutation
- Publication MAF Archive
- mRNA Expression
- Level 3 Data Archives - bcgsc.ca_KIRP.IlluminaHiSeq_miRNASeq.Level_3 [tar.gz] (2.9G)
- mage-tab Data Archives - bcgsc.ca_KIRP.IlluminaHiSeq_miRNASeq.mage-tab [tar.gz]
- miRNA Expression
- Level 3 Data Archives - bcgsc.ca_KIRP.IlluminaHiSeq_miRNASeq.Level_3 [tar.gz] (2.4G)
- mage-tab Data Archives - bcgsc.ca_KIRP.IlluminaHiSeq_miRNASeq.mage-tab [tar.gz]
- Protein Expression
- Level 3 Data Archives - mdanderson.org_KIRP.MDA_RPPA_Core.Level_3 [tar.gz]
- Level 2 Data Archives - mdanderson.org_KIRP.MDA_RPPA_Core.Level_2 [tar.gz]
- Level 1 Data Archives - mdanderson.org_KIRP.MDA_RPPA_Core.Level_1 [tar.gz]
- Mage-tab Data Archives - mdanderson.org_KIRP.MDA_RPPA_Core.mage-tab [tar.gz]
- DNA Copy Number
- Level 3 Data Archives - broad.mit.edu_KIRP.Genome.Level_3 [tar.gz]
- Level 2 Data Archives - broad.mit.edu_KIRP.Genome.Level_2 [tar.gz]
- Level 1 Data Archives - broad.mit.edu_KIRP.Genome.Level_1 [tar.gz]
- Mage-tab Data Archives - broad.mit.edu_KIRP.Genome_Wide_SNP_6.mage-tab [tar.gz]
- DNA Methylation
- Level 3 Data Archives - jhu-usc.edu_KIRP.HumanMethylation.Level_3 [tar.gz](1.4G)
- Level 2 Data Archives - jhu-usc.edu_KIRP.HumanMethylation.Level_2 [tar.gz] (1.3G)
- Level 1 Data Archives - jhu-usc.edu_KIRP.HumanMethylation.Level_1 [tar.gz] (1.4G)
- Mage-tab Data Archives - jhu-usc.edu_KIRP.HumanMethylation.mage-tab [tar.gz]
Additional Resources
- GDC Encyclopedia
- Descriptions of TCGA data are provided in the TCGA Barcode Encyclopedia Page
- Genomic Data Commons Portal
Instructions for Data Download
Open Access Data
- Download the appropriate manifest file from the publication page
- Use the manifest file to download data using the GDC Data Transfer Tool (DTT) or the GDC API
- GDC DTT (Download, User's Guide)
- GDC API (User’s Guide)
Controlled Access Data
- Download the appropriate manifest file from the publication page
- Download a token from the GDC Data Portal
- GDC Data Portal (Launch, User’s Guide)
- Use the manifest file and token to download data using the GDC DTT or the GDC API
- GDC DTT (Download, User’s Guide)
- GDC API (User’s Guide)
For assistance, please contact the GDC Help Desk: support@nci-gdc. datacommons.io.