Evidence map›Paper›PMID 23272139›Full record

ArticlePloS one2012

Association of the innate immunity and inflammation pathway with advanced prostate cancer risk.

Rémi Kazma, Joel A Mefford, Iona Cheng, Sarah J Plummer, Albert M Levin, Benjamin A Rybicki, Graham Casey, John S Witte

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 12% 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

36 citing papers in PubMed, 1 synthesis or guideline pooled it, 59 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Role of Innate Immunity in Cancer.Advances in experimental medicine and biology · 2025
    Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Communications biology · 2018
    Article
  12. Article
  13. Review
  14. Natriuretic Peptides: The Case of Prostate Cancer.Molecules (Basel, Switzerland) · 2017
    Review
  15. Article
  16. Article
  17. Prostate Cancer: Is It a Battle Lost to Age?Geriatrics (Basel, Switzerland) · 2016
    Review
  18. Article
  19. Article
  20. Article
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

8 authors at 5 institutions in 1 country.

Rémi KazmaDepartment of Epidemiology, and Institute for Human Genetics, University of California San Francisco, San Francisco, California, United States of America.
Joel A Mefford
Iona Cheng
Sarah J Plummer
Albert M Levin
Benjamin A Rybicki
Graham Casey
John S Witte
University of California, San Francisco · USUniversity of Southern California · USHenry Ford Health System · USMichigan United · USUniversity of Hawaii System · US

Funding

Training in Molecular& Genetic Epidemiology of CancerR25CA112355 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WITTE, JOHN S. · 2005 to 2018
$6.5M
Genetic Epidemiology of Prostate Cancer Risk and ProgressionR01CA088164 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI VAN DEN EEDEN, STEPHEN K., WITTE, JOHN S. · 2000 to 2015
$6.1M
Genomewide Association Study of Prostate CancerU01CA127298 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WITTE, JOHN S. · 2008 to 2012
$5.1M
NCI NIH HHS R01 CA088164NCI NIH HHS R01CA88164NCI NIH HHS R25 CA112355NCI NIH HHS R25CA112355NCI NIH HHS U01 CA127298NCI NIH HHS U01CA127298
6 · The paper itself

Abstract

Prostate cancer is the most frequent and second most lethal cancer in men in the United States. Innate immunity and inflammation may increase the risk of prostate cancer. To determine the role of innate immunity and inflammation in advanced prostate cancer, we investigated the association of 320 single nucleotide polymorphisms, located in 46 genes involved in this pathway, with disease risk using 494 cases with advanced disease and 536 controls from Cleveland, Ohio. Taken together, the whole pathway was associated with advanced prostate cancer risk (P = 0.02). Two sub-pathways (intracellular antiviral molecules and extracellular pattern recognition) and four genes in these sub-pathways (TLR1, TLR6, OAS1, and OAS2) were nominally associated with advanced prostate cancer risk and harbor several SNPs nominally associated with advanced prostate cancer risk. Our results suggest that the innate immunity and inflammation pathway may play a modest role in the etiology of advanced prostate cancer through multiple small effects.

Indexed as

Immunity, InnateSignal TransductionAgedBlack or African AmericanGenetic Predisposition to DiseaseGenotypeHumansInflammationMaleMiddle AgedNeoplasm GradingNeoplasm StagingPolymorphism, Single NucleotideProstatic NeoplasmsRiskWhite People

Identifiers

PMID23272139
PMCPMC3522730
OpenAlexW2038430331

What OpenQuestion holds

Textmetadata
LicenceCC0
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.