Evidence map›Paper›PMID 23348903›Full record

ArticleModern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc2013

Prostate cancer cell phenotypes based on AGR2 and CD10 expression.

Melissa E Ho, Sue-Ing Quek, Lawrence D True, Colm Morrissey, Eva Corey, Robert L Vessella, Ruth Dumpit, Peter S Nelson, Erin L Maresh, Vei Mah and 7 more

Open access · greenAbstract read
In one paragraph

Article in Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.8field-weighted citation impact, top 7% 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

23 citing papers in PubMed, 32 citations in OpenAlex.

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  6. Article
  7. A New CD10 Antibody Inhibits the Growth of Malignant Mesothelioma.Monoclonal antibodies in immunodiagnosis and immunotherapy · 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

17 authors at 4 institutions in 1 country.

Melissa E HoDepartment of Urology, University of Washington, Seattle, WA 98195-6100, USA.
Sue-Ing Quek
Lawrence D True
Colm Morrissey
Eva Corey
Robert L Vessella
Ruth Dumpit
Peter S Nelson
Erin L Maresh
Vei Mah
Mohammed Alavi
Sara R Kim
Lora Bagryanova
Steve Horvath
David Chia
Lee Goodglick
Alvin Y Liu
University of California, Los Angeles · USUniversity of Washington · USFred Hutch Cancer Center · USVA Puget Sound Health Care System · US

Funding

TRANSCRIPTOME AND PROTEOME STRATIFICATION OF PROSTATE ADENOCARCINOMA PHENOTYPESP50CA097186 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PETER S NELSON · 2002 to 2026
$58.1M
The Early Detection Research Network Biomarker Resource Laboratory at UCLAU24CA086366 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CHIA, DAVID S. · 2000 to 2014
$7.3M
The Early Detection Research Network: Biomarker Developmental LaboratoriesU01CA111244 · NCI · UNIVERSITY OF WASHINGTON · PI LIU, ALVIN Y · 2004 to 2015
$4.1M
NCI NIH HHS CA111244NCI NIH HHS CA86366NCI NIH HHS P50 CA097186NCI NIH HHS U01 CA111244NCI NIH HHS U24 CA086366
6 · The paper itself

Abstract

The combination of expression patterns of AGR2 (anterior gradient 2) and CD10 by prostate cancer provided four phenotypes that correlated with clinical outcome. Based on immunophenotyping, CD10(low)AGR2(high), CD10(high)AGR2(high), CD10(low)AGR2(low), and CD10(high)AGR2(low) were distinguished. AGR2(+) tumors were associated with longer recurrence-free survival and CD10(+) tumors with shorter recurrence-free survival. In high-stage cases, the CD10(low)AGR2(high) phenotype was associated with a ninefold higher recurrence-free survival than the CD10(high)AGR2(low) phenotype. The CD10(high)AGR2(high) and CD10(low)AGR2(low) phenotypes were intermediate. The CD10(high)AGR2(low) phenotype was most frequent in high-grade primary tumors. Conversely, bone and other soft tissue metastases, and derivative xenografts, expressed more AGR2 and less CD10. AGR2 protein was readily detected in tumor metastases. The CD10(high)AGR2(low) phenotype in primary tumors is predictive of poor outcome; however, the CD10(low)AGR2(high) phenotype is more common in metastases. It appears that AGR2 has a protective function in primary tumors but may have a role in the distal spread of tumor cells.

Indexed as

AnimalsBiomarkers, TumorBone NeoplasmsCarcinomaDisease-Free SurvivalHeterograftsHumansImmunohistochemistryImmunophenotypingKaplan-Meier EstimateLymphatic MetastasisMaleMiceMice, Inbred BALB CMice, NudeMucoproteinsAGR2 protein, humanBiomarkers, TumorMucoproteinsNeprilysinOncogene ProteinsProteins

Identifiers

PMID23348903
PMCPMC3638070
OpenAlexW2042887947

What OpenQuestion holds

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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.