Evidence map›Paper›PMID 20670949›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2010

Epithelial membrane protein-2 is a novel therapeutic target in ovarian cancer.

Maoyong Fu, Erin L Maresh, Robert A Soslow, Mohammad Alavi, Vei Mah, Qin Zhou, Alexia Iasonos, Lee Goodglick, Lynn K Gordon, Jonathan Braun and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.6field-weighted citation impact, top 8% 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

25 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
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  6. Review
  7. EMP3: A promising biomarker for tumor prognosis and targeted cancer therapy.Cancer biomarkers : section A of Disease markers · 2024
    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

11 authors at 2 institutions in 1 country.

Maoyong FuDepartment of Pathology and Laboratory Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA 90095, USA.
Erin L Maresh
Robert A Soslow
Mohammad Alavi
Vei Mah
Qin Zhou
Alexia Iasonos
Lee Goodglick
Lynn K Gordon
Jonathan Braun
Madhuri Wadehra
Memorial Sloan Kettering Cancer Center · USUCLA Jonsson Comprehensive Cancer Center

Funding

Women's CancersP30CA016042 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Samuel Wheeler French · 1985 to 2026
$134.5M
Stanford Nanocharacterization LaboratoryU54CA119367 · NCI · STANFORD UNIVERSITY · PI GAMBHIR, SANJIV S · 2006 to 2010
$19.8M
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
Targeting EMP2 in Endometrial CancerR21CA131756 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WADEHRA, MADHURI · 2009 to 2010
$373k
Abnormal EMPS Expression Affects Pregnancy OutcomeR03HD048540 · NICHD · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI BRAUN, JONATHAN · 2005 to 2006
$305k
NCI NIH HHS CA016042NCI NIH HHS NCI CA-86366NCI NIH HHS P30 CA016042NCI NIH HHS R21 CA131756NCI NIH HHS U24 CA086366NCI NIH HHS U54 CA119367NICHD NIH HHS HD48540NICHD NIH HHS R03 HD048540
6 · The paper itself

Abstract

purposeThe tetraspan protein epithelial membrane protein-2 (EMP2) has been shown to regulate the surface display and signaling from select integrin pairs, and it was recently identified as a prognostic biomarker in human endometrial cancer. In this study, we assessed the role of EMP2 in human ovarian cancer. EXPERIMENTAL

designWe examined the expression of EMP2 within a population of women with ovarian cancer using tissue microarray assay technology. We evaluated the efficacy of EMP2-directed antibody therapy using a fully human recombinant bivalent antibody fragment (diabody) in vitro and ovarian cancer xenograft models in vivo.

resultsEMP2 was found to be highly expressed in >70% of serous and endometrioid ovarian tumors compared with nonmalignant ovarian epithelium using a human ovarian cancer tissue microarray. Using anti-EMP2 diabody, we evaluated the in vitro response of nine human ovarian cancer cell lines with detectable EMP2 expression. Treatment of human ovarian cancer cell lines with anti-EMP2 diabodies induced cell death and retarded cell growth, and these response rates correlated with cellular EMP2 expression. We next assessed the effects of anti-EMP2 diabodies in mice bearing xenografts from the ovarian endometrioid carcinoma cell line OVCAR5. Anti-EMP2 diabodies significantly suppressed tumor growth and induced cell death in OVCAR5 xenografts.

conclusionsThese findings indicate that EMP2 is expressed in the majority of ovarian tumors and may be a feasible target in vivo.

Indexed as

AdultAgedAnimalsAntineoplastic AgentsBlotting, WesternFemaleGene ExpressionGene Expression ProfilingHumansImmunoglobulin FragmentsImmunohistochemistryImmunotherapyMembrane GlycoproteinsMiceMice, NudeMiddle AgedAntineoplastic AgentsEMP2 protein, humanImmunoglobulin FragmentsMembrane Glycoproteins

Identifiers

PMID20670949
PMCPMC2913478
OpenAlexW2131480102

What OpenQuestion holds

Textmetadata
LicenceTDM
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.