Evidence map›Paper›PMID 23610450›Full record

ArticleCancer research2013

Animal models of human prostate cancer: the consensus report of the New York meeting of the Mouse Models of Human Cancers Consortium Prostate Pathology Committee.

Michael Ittmann, Jiaoti Huang, Enrico Radaelli, Philip Martin, Sabina Signoretti, Ruth Sullivan, Brian W Simons, Jerrold M Ward, Brian D Robinson, Gerald C Chu and 4 more

Open access · bronzeAbstract readConsensus Statement
In one paragraph

Article in Cancer research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 154 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
154citing papers in PubMed, 1 pooled it
18.5field-weighted citation impact, top 1% 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

154 citing papers in PubMed, 1 synthesis or guideline pooled it, 236 citations in OpenAlex.

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94 more citing papers are in PubMed but not listed here.

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 5 institutions in 1 country.

Michael IttmannDepartment of Pathology and Immunology, Baylor College of Medicine, Texas 77030, USA. mittmann@bcm.edu
Jiaoti Huang
Enrico Radaelli
Philip Martin
Sabina Signoretti
Ruth Sullivan
Brian W Simons
Jerrold M Ward
Brian D Robinson
Gerald C Chu
Massimo Loda
George Thomas
Alexander Borowsky
Robert D Cardiff
Frederick National Laboratory for Cancer Research · USJohns Hopkins University · USUniversity of California, Davis · USUniversity of California, Los Angeles · USBaylor College of Medicine · US

Funding

UW COMPREHENSIVE CANCER CENTER SUPPORTP30CA014520 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI AMY TRENTHAM-DIETZ · 1985 to 2026
$142.6M
Staff InvestigatorsP30CA093373 · NCI · UNIVERSITY OF CALIFORNIA DAVIS · PI Laura Marcu · 2002 to 2026
$84.9M
Tumor BiologyP30CA125123 · NCI · BAYLOR COLLEGE OF MEDICINE · PI DAVID R ROWLEY · 2007 to 2026
$73.9M
Understanding the origins of rapid recurrence of pancreatic cancer after resectionP30CA069533 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI Luiz Eduardo Bertassoni · 1997 to 2026
$60.5M
Transgenic Mouse CoreP01CA089021 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI SELLERS, WILLIAM R · 2001 to 2011
$20.1M
Mechanisms of breast cancer progressionU01CA105490 · NCI · UNIVERSITY OF PENNSYLVANIA · PI CHODOSH, LEWIS A · 2004 to 2013
$6.7M
Molecular Link Between Metabolic Syndrome and Prostate CancerR01CA131945 · NCI · DANA-FARBER CANCER INST · PI LODA, MASSIMO · 2008 to 2018
$4.0M
The Center for Translational Genomic PhenotypingU01CA141582 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI CARDIFF, ROBERT D, CHERRY, SIMON R · 2009 to 2013
$3.5M
Role of FGFR1 signaling in distinct cell lineages in prostate cancer progresssionU01CA141497 · NCI · BAYLOR COLLEGE OF MEDICINE · PI ITTMANN, MICHAEL M · 2009 to 2013
$3.4M
Inhibiting VHL-positive kidney cancerR01CA169172 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI THOMAS, GEORGE VICTOR · 2013 to 2017
$1.6M
Baylor College of Medicine Cancer CenterP20CA103698 · NCI · BAYLOR COLLEGE OF MEDICINE · PI OSBORNE, C KENT · 2003 to 2005
$1.2M
NCI NIH HHS P01 CA089021NCI NIH HHS P01 CA89021NCI NIH HHS P20 CA103698NCI NIH HHS P30 CA014520NCI NIH HHS P30 CA069533NCI NIH HHS P30 CA069533 13S5NCI NIH HHS P30 CA093373NCI NIH HHS P30 CA125123NCI NIH HHS P30CA125123NCI NIH HHS R01 CA131945NCI NIH HHS R01 CA169172NCI NIH HHS U01 CA105490NCI NIH HHS U01 CA141497NCI NIH HHS U01CA141497NCI NIH HHS U01 CA141582
6 · The paper itself

Abstract

Animal models, particularly mouse models, play a central role in the study of the etiology, prevention, and treatment of human prostate cancer. While tissue culture models are extremely useful in understanding the biology of prostate cancer, they cannot recapitulate the complex cellular interactions within the tumor microenvironment that play a key role in cancer initiation and progression. The National Cancer Institute (NCI) Mouse Models of Human Cancers Consortium convened a group of human and veterinary pathologists to review the current animal models of prostate cancer and make recommendations about the pathologic analysis of these models. More than 40 different models with 439 samples were reviewed, including genetically engineered mouse models, xenograft, rat, and canine models. Numerous relevant models have been developed over the past 15 years, and each approach has strengths and weaknesses. Analysis of multiple genetically engineered models has shown that reactive stroma formation is present in all the models developing invasive carcinomas. In addition, numerous models with multiple genetic alterations display aggressive phenotypes characterized by sarcomatoid carcinomas and metastases, which is presumably a histologic manifestation of epithelial-mesenchymal transition. The significant progress in development of improved models of prostate cancer has already accelerated our understanding of the complex biology of prostate cancer and promises to enhance development of new approaches to prevention, detection, and treatment of this common malignancy.

Indexed as

Disease Models, AnimalGene Expression Regulation, NeoplasticAdenocarcinomaAnimalsDisease ProgressionGenetic EngineeringHumansMaleMiceNeoplasm MetastasisNeoplasm TransplantationNew YorkOncogenesProstatic NeoplasmsRatsSocieties, Medical

Identifiers

PMID23610450
PMCPMC3644021
OpenAlexW2125819870

What OpenQuestion holds

Textmetadata
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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.