Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Evaluation of 8q24 and 17q risk loci and prostate cancer mortality.

Clinical cancer research : an official journal of the American Association for Cancer Research - 1 May 2009

Penney Kathryn L, Salinas Claudia A, Pomerantz Mark, Schumacher Fredrick R, Beckwith Christine A, Lee Gwo-Shu, Oh William K, Sartor Oliver, Ostrander Elaine A, Kurth Tobias, Ma Jing, Mucci Lorelei, Stanford Janet L, Kantoff Philip W, Hunter David J, Stampfer Meir J, Freedman Matthew L

Abstract excerpt

PURPOSE: Variants at chromosomal loci 8q24 and 17q are established risk factors for prostate cancer. Many studies have confirmed the findings for risk, but few have examined aggressiveness and other clinical variables in detail. Additionally, Gleason score is typically used as a surrogate for the primary end point of prostate cancer mortality. We investigated whether the 8q24 and 17q risk variants are associated...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Case-Control Studies
Share to Chromosomes, Human, Pair 17

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 8

Share to Cohort Studies

Share to Incidence

Share to Neoplasm Staging

Share to Prostatic Neoplasms

Share to Survival Rate

Source

Open in PubMed Open full text

Identifiers

PMID: 19366828
DOI: 10.1158/1078-0432.CCR-08-2733
PMCID: PMC2878092

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Evaluation of 8q24 and 17q risk loci and prostate cancer mortality.PMID 19366828Read ↗

Association of prostate cancer risk Loci with disease aggressiveness and prostate cancer-specific mortality.Semantic proximity Read ↗

Association between sequence variants at 17q12 and 17q24.3 and prostate cancer risk in European and African Americans.Semantic proximity Read ↗

New variants at 10q26 and 15q21 are associated with aggressive prostate cancer in a genome-wide association study from a prostate biopsy screening cohort.Semantic proximity Read ↗

Pathological outcomes associated with the 17q prostate cancer risk variants.Semantic proximity Read ↗

8q24 genetic variation and comprehensive haplotypes altering familial risk of prostate cancer.Semantic proximity Read ↗

Sequence variants at 22q13 are associated with prostate cancer risk.Semantic proximity Read ↗

Chromosome 17q12 variants contribute to risk of early-onset prostate cancer.Semantic proximity Read ↗

Associations of prostate cancer risk variants with disease aggressiveness: results of the NCI-SPORE Genetics Working Group analysis of 18,343 cases.Semantic proximity Read ↗

Inherited genetic variant predisposes to aggressive but not indolent prostate cancer.Semantic proximity Read ↗

Clinical utility of five genetic variants for predicting prostate cancer risk and mortality.Semantic proximity Read ↗

Prospective study of DNA methylation at chromosome 8q24 in peripheral blood and prostate cancer risk.Semantic proximity Read ↗

Multiple independent genetic variants in the 8q24 region are associated with prostate cancer risk.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.