Evidence map›Paper›PMID 20333727›Full record

ArticleThe Prostate2010

Genome-wide linkage analysis of 1,233 prostate cancer pedigrees from the International Consortium for Prostate Cancer Genetics using novel sumLINK and sumLOD analyses.

G Bryce Christensen, Agnes B Baffoe-Bonnie, Asha George, Isaac Powell, Joan E Bailey-Wilson, John D Carpten, Graham G Giles, John L Hopper, Gianluca Severi, Dallas R English and 37 more

Abstract read
In one paragraph

Article in The Prostate, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

13 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Prostate Cancer Radiogenomics-From Imaging to Molecular Characterization.International journal of molecular sciences · 2021
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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

47 authors.

G Bryce ChristensenUniversity of Utah ICPCG Group and Division of Genetic Epidemiology, University of Utah School of Medicine, Salt Lake City, Utah 84108, USA. bryce.christensen@utah.edu
Agnes B Baffoe-Bonnie
Asha George
Isaac Powell
Joan E Bailey-Wilson
John D Carpten
Graham G Giles
John L Hopper
Gianluca Severi
Dallas R English
William D Foulkes
Lovise Maehle
Pal Moller
Ros Eeles
Douglas Easton
Michael D Badzioch
Alice S Whittemore
Ingrid Oakley-Girvan
Chih-Lin Hsieh
Latchezar Dimitrov
Jianfeng Xu
Janet L Stanford
Bo Johanneson
Kerry Deutsch
Laura McIntosh
Elaine A Ostrander
Kathleen E Wiley
Sarah D Isaacs
Patrick C Walsh
William B Isaacs
Stephen N Thibodeau
Shannon K McDonnell
Scott Hebbring
Daniel J Schaid
Ethan M Lange
Kathleen A Cooney
Teuvo L J Tammela
Johanna Schleutker
Thomas Paiss
Christiane Maier
Henrik Grönberg
Fredrik Wiklund
Monica Emanuelsson
James M Farnham
Lisa A Cannon-Albright
Nicola J Camp
International Consortium for Prostate Cancer Genetics

Funding

WORD PROCESSING CENTER--COREP30CA006927 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI Margaret von Mehren · 1985 to 2026
$138.8M
UTAH REGIONAL CANCER CENTERP30CA042014 · NCI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Jared P Rutter · 1986 to 2026
$72.6M
Prostate Cancer Susceptibility: The ICPCG StudyU01CA089600 · NCI · MAYO CLINIC ROCHESTER · PI THIBODEAU, STEPHEN NORMAN · 2002 to 2016
$27.3M
UNIVERSITY OF UTAH MEDICAL INFORMATICS TRAININGT15LM007124 · NLM · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Karen Louise Eilbeck · 1997 to 2026
$22.0M
VIRAL DAMAGE TO BRAIN AND NEUROMUSCULAR SYSTEMM01RR000064 · NCRR · UNIVERSITY OF UTAH · PI SWOBODA, KATHRYN J. · 1985 to 2008
$21.7M
STRUCTURAL/FUNCTIONAL CHARACTERIZATION OF AMINOGLYCOSIDEG12RR003048 · NCRR · HOWARD UNIVERSITY · PI SOUTHERLAND, WILLIAM M. · 1985 to 2011
$19.0M
Genetic Epidemiology of CancerZIAHG200331 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI BAILEY-WILSON, JOAN ELLEN · 2009 to 2022
$11.7M
GENETIC EPIDEMIOLOGY OF PROSTATE CANCERR01CA080122 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI STANFORD, JANET L · 1999 to 2008
$3.8M
GENETICS OF PROSTATE CANCER SUSCEPTIBILITYR01CA078836 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI NELSON, PETER S · 1999 to 2005
$3.3M
GENETIC ANALYSIS OF HEREDITARY PROSTATE CANCER FAMILIESR01CA079596 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI COONEY, KATHLEEN A · 1999 to 2009
$3.0M
Mapping and Cloning Prostate Cancer Predisposition LociR01CA090752 · NCI · UNIVERSITY OF UTAH · PI ALBRIGHT, LISA CANNON · 2001 to 2004
$2.3M
LOCALIZATION OF SUSCEPTIBILITY LOCI IN PROSTATE CANCERR01CA072818 · NCI · MAYO CLINIC COLL OF MEDICINE, ROCHESTER · PI THIBODEAU, STEPHEN NORMAN · 1997 to 2005
$1.9M
Cancer Research UK 10118Cancer Research UK 11022Medical Research Council G0802851NCI NIH HHS CA98364NCI NIH HHS K07 CA098364NCI NIH HHS N01 PC035141NCI NIH HHS P30 CA006927NCI NIH HHS P30 CA042014NCI NIH HHS R01 CA067044NCI NIH HHS R01 CA072818NCI NIH HHS R01 CA078836NCI NIH HHS R01 CA079596NCI NIH HHS R01 CA080122NCI NIH HHS R01 CA090752NCI NIH HHS R01 CA095052NCI NIH HHS R01 CA106523NCI NIH HHS U01 CA067044NCI NIH HHS U01 CA089600NCI NIH HHS U01 CA89600NCRR NIH HHS G12 RR003048NCRR NIH HHS M01 RR000064NHGRI NIH HHS N01 HG065403NHGRI NIH HHS N01 HG075418NLM NIH HHS T15 LM007124NLM NIH HHS T15 LM07124
6 · The paper itself

Abstract

backgroundProstate cancer (PC) is generally believed to have a strong inherited component, but the search for susceptibility genes has been hindered by the effects of genetic heterogeneity. The recently developed sumLINK and sumLOD statistics are powerful tools for linkage analysis in the presence of heterogeneity.

methodsWe performed a secondary analysis of 1,233 PC pedigrees from the International Consortium for Prostate Cancer Genetics (ICPCG) using two novel statistics, the sumLINK and sumLOD. For both statistics, dominant and recessive genetic models were considered. False discovery rate (FDR) analysis was conducted to assess the effects of multiple testing.

resultsOur analysis identified significant linkage evidence at chromosome 22q12, confirming previous findings by the initial conventional analyses of the same ICPCG data. Twelve other regions were identified with genome-wide suggestive evidence for linkage. Seven regions (1q23, 5q11, 5q35, 6p21, 8q12, 11q13, 20p11-q11) are near loci previously identified in the initial ICPCG pooled data analysis or the subset of aggressive PC pedigrees. Three other regions (1p12, 8p23, 19q13) confirm loci reported by others, and two (2p24, 6q27) are novel susceptibility loci. FDR testing indicates that over 70% of these results are likely true positive findings. Statistical recombinant mapping narrowed regions to an average of 9 cM.

conclusionsOur results represent genomic regions with the greatest consistency of positive linkage evidence across a very large collection of high-risk PC pedigrees using new statistical tests that deal powerfully with heterogeneity. These regions are excellent candidates for further study to identify PC predisposition genes.

Indexed as

Genetic LinkagePedigreeChromosome MappingChromosomes, Human, Pair 22Genetic Predisposition to DiseaseGenome, HumanGenome-Wide Association StudyGenotypeHumansMaleProstatic Neoplasms

Identifiers

PMID20333727
PMCPMC3428045

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Registered trials

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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.