ID

45494

Description

Principal Investigator: Levi Garraway, M.D. Ph.D, Dana Farber Cancer Institute, Boston, MA USA; Broad Institute, Cambridge, MA USA MeSH: Prostatic Neoplasms https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000447 Prostate cancer is a prevalent cause of cancer morbidity and mortality in men. In order to characterize the full range of somatic mutations in protein-coding genes that may drive the growth of prostate cancer, we sequenced the exonic regions of genomic and tumor DNA from over 100 patients with high-risk primary prostate cancer. Using hybrid capture and paired end DNA sequencing, we identified mutations in several novel putative prostate cancer genes. We interrogated copy number changes across tumor genomes using high-density SNP arrays, and identified a molecular subtype of cancer characterized by mutation of the ubiquitin ligase subunit SPOP and copy number loss at specific genomic loci.

Link

dbGap study = phs000447

Keywords

  1. 10/24/22 10/24/22 - Simon Heim
  2. 12/13/22 12/13/22 - Kristina Keller
Copyright Holder

Levi Garraway, M.D. Ph.D, Dana Farber Cancer Institute, Boston, MA USA; Broad Institute, Cambridge, MA USA

Uploaded on

December 13, 2022

DOI

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License

Creative Commons BY 4.0

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dbGaP phs000447 Prostate Cancer Genome Sequencing Project

Eligibility Criteria

Inclusion and exclusion criteria
Description

Inclusion and exclusion criteria

Primary prostate tumors from patients undergoing surgery for localized prostate cancer were selected based on high density of tumor tissue. DNA was extracted from prostate tumor tissue and from either adjacent normal prostate or blood for use as a normal DNA comparator. DNA was assessed for high quality and integrity on Affymetrix SNP 6.0 arrays and by agarose gel electrophoresis.
Description

Primary prostate tumors from patients undergoing surgery for localized prostate cancer were selected based on high density of tumor tissue. DNA was extracted from prostate tumor tissue and from either adjacent normal prostate or blood for use as a normal DNA comparator. DNA was assessed for high quality and integrity on Affymetrix SNP 6.0 arrays and by agarose gel electrophoresis.

Data type

boolean

Alias
UMLS CUI [1,1]
C0475358
UMLS CUI [1,2]
C0194790
UMLS CUI [1,3]
C1268672
UMLS CUI [1,4]
C0949542
UMLS CUI [2,1]
C3839098
UMLS CUI [2,2]
C0033578
UMLS CUI [2,3]
C0220825
UMLS CUI [2,4]
C4085938
UMLS CUI [2,5]
C1527094
UMLS CUI [2,6]
C0013856

Similar models

Eligibility Criteria

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Inclusion and exclusion criteria
Primary prostate tumors from patients undergoing surgery for localized prostate cancer were selected based on high density of tumor tissue. DNA was extracted from prostate tumor tissue and from either adjacent normal prostate or blood for use as a normal DNA comparator. DNA was assessed for high quality and integrity on Affymetrix SNP 6.0 arrays and by agarose gel electrophoresis.
Item
Primary prostate tumors from patients undergoing surgery for localized prostate cancer were selected based on high density of tumor tissue. DNA was extracted from prostate tumor tissue and from either adjacent normal prostate or blood for use as a normal DNA comparator. DNA was assessed for high quality and integrity on Affymetrix SNP 6.0 arrays and by agarose gel electrophoresis.
boolean
C0475358 (UMLS CUI [1,1])
C0194790 (UMLS CUI [1,2])
C1268672 (UMLS CUI [1,3])
C0949542 (UMLS CUI [1,4])
C3839098 (UMLS CUI [2,1])
C0033578 (UMLS CUI [2,2])
C0220825 (UMLS CUI [2,3])
C4085938 (UMLS CUI [2,4])
C1527094 (UMLS CUI [2,5])
C0013856 (UMLS CUI [2,6])

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