Evidence map›Paper›PMID 18767027›Full record

ArticleThe Prostate2008

Association of HPC2/ELAC2 and RNASEL non-synonymous variants with prostate cancer risk in African American familial and sporadic cases.

Christiane M Robbins, Wenndy Hernandez, Chiledum Ahaghotu, James Bennett, Gerald Hoke, Terry Mason, Curtis A Pettaway, Srinivasan Vijayakumar, Sally Weinrich, Paulette Furbert-Harris and 4 more

Abstract read
In one paragraph

Article in The Prostate, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 4 pooled it
2.5field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

25 citing papers in PubMed, 4 syntheses or guidelines pooled it, 33 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Trial
  6. Association of selectedPathology oncology research : POR · 2026
    Article
  7. Article
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  10. Review
  11. Review
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  13. Article
  14. Molecular pathways in prostate cancer.Nephro-urology monthly · 2013
    Review
  15. A single nucleotide polymorphism in inflammatory gene RNASEL predicts outcome after radiation therapy for localized prostate cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2013
    Article
  16. Systems genetics in "-omics" era: current and future development.Theory in biosciences = Theorie in den Biowissenschaften · 2013
    Review
  17. Article
  18. Article
  19. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 9 institutions in 1 country.

Christiane M RobbinsTranslational Genomics Research Institute, Division of Integrated Cancer Genomics, Phoenix, Arizona 85004, USA.
Wenndy Hernandez
Chiledum Ahaghotu
James Bennett
Gerald Hoke
Terry Mason
Curtis A Pettaway
Srinivasan Vijayakumar
Sally Weinrich
Paulette Furbert-Harris
Georgia Dunston
Isaac J Powell
John D Carpten
Rick A Kittles
Howard University · USTranslational Genomics Research Institute · USUniversity of Chicago · USAugusta University · USEmory University Hospital Midtown · USNewYork–Presbyterian Hospital · USThe Barbara Ann Karmanos Cancer Institute · USThe University of Texas MD Anderson Cancer Center · USUniversity of California, Davis · US

Funding

AFRICAN AMERICAN HEREDITARY PROSTATE CANCER STUDYN01HG075418 · NHGRI · HOWARD UNIVERSITY · PI DUNSTON, GEORGIA M · 1997 to 1999
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NHGRI NIH HHS 1-HG-75418NHGRI NIH HHS N01 HG075418
6 · The paper itself

Abstract

introductionThe RNASEL and HPC2/ELAC2 genes have been implicated in hereditary prostate cancer. Further assessment of the role of these genes in sporadic prostate cancer in African American men (AAM) is warranted.

methodsGenotyping of HPC2/ELAC2 variants (S217L, A541T), along with RNASEL variants (R462Q and E541D) was completed in 155 African American sporadic and 88 familial prostate cancer cases, and 296 healthy male controls. Logistic regression analysis was performed and odds ratios (OR) were calculated, while correcting for both age and population stratification using admixture informative markers.

resultsThe HPC2/ELAC2 217L allele was significantly associated with risk of prostate cancer when taking all cases into account (OR = 1.6; 1.0-2.6; P = 0.03). The RNASEL 541D allele was associated with a decrease in risk of prostate cancer in sporadic cases (OR = 0.4; 0.2-0.8; P = 0.01). We did not detect an association between prostate cancer risk and the RNASEL R462Q variant. Results from haplotype analyses of the two RNASEL variants revealed highly significant differences in haplotype allele frequencies between cases and controls suggesting a synergistic effect at the RNASEL locus. One haplotype in particular (462R-541D) is far more frequent in our control population and shows a strong protective effect against prostate cancer (OR = 0.47, P = 8.1 x 10(-9)).

conclusionsThese results suggest that HPC2/ELAC2 and RNASEL may play a role, however minor, in prostate cancer risk among AAM.

Indexed as

AdultAgedAged, 80 and overBlack or African AmericanCase-Control StudiesEndoribonucleasesGene FrequencyGenetic Predisposition to DiseaseGenotypeHaplotypesHumansLogistic ModelsMaleMiddle AgedNeoplasm ProteinsPolymorphism, Single Nucleotide2-5A-dependent ribonucleaseELAC2 protein, humanEndoribonucleasesNeoplasm Proteins

Identifiers

PMID18767027
PMCPMC4097307
OpenAlexW1989532247

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.