Evidence map›Paper›PMID 19773449›Full record

ArticleCancer research2009

Comparative analyses of chromosome alterations in soft-tissue metastases within and across patients with castration-resistant prostate cancer.

Ilona N Holcomb, Janet M Young, Ilsa M Coleman, Keyan Salari, Douglas I Grove, Li Hsu, Lawrence D True, Martine P Roudier, Colm M Morrissey, Celestia S Higano and 3 more

Abstract read
In one paragraph

Article in Cancer research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
5.5field-weighted citation impact, top 4% 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

38 citing papers in PubMed, 1 synthesis or guideline pooled it, 66 citations in OpenAlex.

  1. Pooled it
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  19. Genomic profiling defines subtypes of prostate cancer with the potential for therapeutic stratification.Clinical cancer research : an official journal of the American Association for Cancer Research · 2013
    Review
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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

13 authors at 5 institutions in 2 countries.

Ilona N HolcombDivisions of Human Biology, Fred Hutchinson Cancer Research Center, University of Washington, Seattle, Washington, USA.
Janet M Young
Ilsa M Coleman
Keyan Salari
Douglas I Grove
Li Hsu
Lawrence D True
Martine P Roudier
Colm M Morrissey
Celestia S Higano
Peter S Nelson
Robert L Vessella
Barbara J Trask
Neurology, Inc · USUniversity of Washington · USCancer Research Center · USFred Hutch Cancer Center · USStanford University · US

Funding

TRANSCRIPTOME AND PROTEOME STRATIFICATION OF PROSTATE ADENOCARCINOMA PHENOTYPESP50CA097186 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI RUTH D ETZIONI · 2002 to 2026
$58.1M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM007365 · NIGMS · STANFORD UNIVERSITY · PI CHUA, KATRIN F · 1985 to 2021
$33.8M
INTERDISCIPLINARY TRAINING IN GENOMIC SCIENCEST32HG000035 · NHGRI · UNIVERSITY OF WASHINGTON · PI Bruce Colston Trapnell · 1995 to 2026
$24.2M
Transmembrane Proteases and Prostate CarcinogenesisP01CA085859 · NCI · UNIVERSITY OF WASHINGTON · PI VESSELLA, ROBERT LOUIS · 2002 to 2013
$21.2M
Structural, functional genomics olfactory receptor genesR01DC004209 · NIDCD · UNIVERSITY OF WASHINGTON · PI TRASK, BARBARA J. · 1999 to 2008
$5.9M
Statistical Methods in Genetic EpidemiologyR01AG014358 · NIA · FRED HUTCHINSON CANCER RESEARCH CENTER · PI HSU, LI · 2002 to 2013
$2.4M
Gene Copy Number Changes and Breast Cancer SurvivalR01CA098415 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PORTER, PEGGY L. · 2004 to 2008
$2.2M
Molecular Alterations in Lobular/Ductal Breast CancerR01CA095717 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PORTER, PEGGY L · 2002 to 2005
$1.5M
Development of a Urological CD Cell Typing SystemR01DK069690 · NIDDK · FRED HUTCHINSON CANCER RESEARCH CENTER · PI NELSON, PETER S · 2006 to 2009
$1.3M
BAC RESOURCE FOR CYTOGENIC ANALYSES OF HUMAN GENOMEU24CA080295 · NCI · UNIVERSITY OF WASHINGTON · PI TRASK, BARBARA J. · 1998 to 2001
$499k
NCI NIH HHS CA97186NCI NIH HHS P01 CA085859NCI NIH HHS P50 CA097186NCI NIH HHS R01 CA095717NCI NIH HHS R01 CA098415NCI NIH HHS R01CA098415NCI NIH HHS R01 CA95717NCI NIH HHS U24 CA080295NCI NIH HHS U24 CA80295NHGRI NIH HHS T32 HG000035NHGRI NIH HHS T32 HG00035NIA NIH HHS R01 AG014358NIA NIH HHS R01 AG14358NIDCD NIH HHS R01 DC004209NIDCD NIH HHS R01DC004209NIDDK NIH HHS R01 DK069690NIGMS NIH HHS R01 GM07365NIGMS NIH HHS T32 GM007365
6 · The paper itself

Abstract

Androgen deprivation is the mainstay of therapy for progressive prostate cancer. Despite initial and dramatic tumor inhibition, most men eventually fail therapy and die of metastatic castration-resistant (CR) disease. Here, we characterize the profound degree of genomic alteration found in CR tumors using array comparative genomic hybridization (array CGH), gene expression arrays, and fluorescence in situ hybridization (FISH). Bycluster analysis, we show that the similarity of the genomic profiles from primary and metastatic tumors is driven by the patient. Using data adjusted for this similarity, we identify numerous high-frequency alterations in the CR tumors, such as 8p loss and chromosome 7 and 8q gain. By integrating array CGH and expression array data, we reveal genes whose correlated values suggest they are relevant to prostate cancer biology. We find alterations that are significantly associated with the metastases of specific organ sites, and others with CR tumors versus the tumors of patients with localized prostate cancer not treated with androgen deprivation. Within the high-frequency sites of loss in CR metastases, we find an overrepresentation of genes involved in cellular lipid metabolism, including PTEN. Finally, using FISH, we verify the presence of a gene fusion between TMPRSS2 and ERG suggested by chromosome 21 deletions detected by array CGH. We find the fusion in 54% of our CR tumors, and 81% of the fusion-positive tumors contain cells with multiple copies of the fusion. Our investigation lays the foundation for a better understanding of and possible therapeutic targets for CR disease, the poorly responsive and final stage of prostate cancer.

Indexed as

Chromosome AberrationsAgedAged, 80 and overCluster AnalysisComparative Genomic HybridizationGene DosageGene Expression ProfilingHumansIn Situ Hybridization, FluorescenceMaleMiddle AgedOncogene Proteins, FusionOrchiectomyProstatic NeoplasmsSoft Tissue NeoplasmsOncogene Proteins, FusionTMPRSS2-ERG fusion protein, human

Identifiers

PMID19773449
PMCPMC2771763
OpenAlexW2128949248

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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.