Evidence map›Paper›PMID 10825281›Full record

ArticleAmerican journal of human genetics2000

Genomewide scan for prostate cancer-aggressiveness loci.

J S Witte, K A Goddard, D V Conti, R C Elston, J Lin, B K Suarez, K W Broman, J K Burmester, J L Weber, W J Catalona

Open access · bronzeAbstract read
In one paragraph

Article in American journal of human genetics, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
10.0field-weighted citation impact, top 2% 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

50 citing papers in PubMed, 159 citations in OpenAlex.

  1. Genome-wide association study identifies a genetic variant associated with risk for more aggressive prostate cancer.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2011
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  20. Genome-wide association study of prostate cancer mortality.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2010
    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

10 authors at 3 institutions in 1 country.

J S WitteDepartment of Epidemiology and Biostatistics, Case Western Reserve University, Cleveland, OH 44109, USA. witte@darwin.cwru.edu
K A Goddard
D V Conti
R C Elston
J Lin
B K Suarez
K W Broman
J K Burmester
J L Weber
W J Catalona
Case Western Reserve University · USMarshfield Clinic · USWashington University in St. Louis · US

Funding

X-LINKED EXTENSION OF THE REVISED HASEMAN-ELSTON ALGORITHM FOR LINKAGE ANALYSISP41RR003655 · NCRR · LOUISIANA STATE UNIV HSC NEW ORLEANS · PI ELSTON, ROBERT C. · 1987 to 2011
$11.5M
MAMMALIAN GENOTYPING SERVICEN01HV048141 · HV · MARSHFIELD CLINIC RESEARCH FOUNDATION · PI WEBER, JAMES L. · 1994 to 2000
$3.1M
GENETIC ANALYSIS OF MULTIFACTORIAL TRAITSR37GM028356 · NIGMS · CASE WESTERN RESERVE UNIVERSITY · PI ELSTON, ROBERT C. · 1998 to 2007
$2.9M
EPIDEMIOLOGICAL GENETICS AND FAMILY STUDYP30MH031302 · NIMH · WASHINGTON UNIVERSITY · PI CLONINGER, C. ROBERT · 1996 to 2000
$1.0M
HIERARCHICAL MODELING IN CANCER RESEARCHR29CA073270 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI WITTE, JOHN S · 1996 to 2000
$107k
THE MODELLING OF MULTI-LOCUS NATURAL SELECTION--COREP50MH031302 · NIMH · WASHINGTON UNIVERSITY · PI CLONINGER, C. ROBERT · 1985 to 1995
–
GENETIC ANALYSIS OF MULTIFACTORIAL TRAITSR01GM028356 · NIGMS · LOUISIANA STATE UNIV HSC NEW ORLEANS · PI ELSTON, ROBERT C. · 1985 to 1997
–
NCI NIH HHS CA73270NCI NIH HHS R29 CA073270NCRR NIH HHS P41 RR003655NHLBI NIH HHS N01 HV048141NIGMS NIH HHS GM28356NIGMS NIH HHS R01 GM028356NIGMS NIH HHS R37 GM028356NIMH NIH HHS MH31302
6 · The paper itself

Abstract

The aggressiveness of prostate cancer (PCa) varies widely: some tumors progress to invasive, potentially life-threatening disease, whereas others stay latent for the remainder of an individual's lifetime. The mechanisms resulting in this variability are not yet understood, but they are likely to involve both genetic and environmental influences. To investigate genetic factors, we conducted a genomewide linkage analysis of 513 brothers with PCa, using the Gleason score, which reflects tumor histology, as a quantitative measure of PCa aggressiveness. To our knowledge, this is the first time that a measure of PCa aggressiveness has been directly investigated as a quantitative trait in a genomewide scan. We employed a generalized multipoint Haseman-Elston linkage-analysis approach that regresses the mean-corrected cross product between the brothers' Gleason scores on the estimated proportion of alleles shared by brothers identical by descent at each marker location. Our results suggest that candidate regions on chromosomes 5q, 7q, and 19q give evidence for linkage to PCa-aggressiveness genes. In particular, the strongest signals detected in these regions were at the following markers (with corresponding P values): for chromosome 5q31-33, between markers D5S1480 and D5S820 (P=.0002); for chromosome 7q32, between markers D7S3061 and D7S1804 (P=.0007); and, for chromosome 19q12, at D19S433 (P=.0004). This indicates that one or more of these candidate regions may contain genes that influence the progression of PCa from latent to invasive disease. Identification of such genes would be extremely valuable for elucidation of the mechanism underlying PCa progression and for determination of treatment in men in whom this disease has been diagnosed.

Indexed as

AdultAgedAged, 80 and overChromosome MappingChromosomes, HumanGenetic LinkageGenetic MarkersGenetic TestingGenome, HumanHumansMaleMatched-Pair AnalysisMiddle AgedNeoplasm InvasivenessNuclear FamilyPhenotypeGenetic Markers

Identifiers

PMID10825281
PMCPMC1287106
OpenAlexW2099752477

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.