Evidence map›Paper›PMID 24448822›Full record

ArticleMolecular cancer therapeutics2014

Rationale and preclinical efficacy of a novel anti-EMP2 antibody for the treatment of invasive breast cancer.

Maoyong Fu, Erin L Maresh, Gustavo F Helguera, Meagan Kiyohara, Yu Qin, Negin Ashki, Tracy R Daniels-Wells, Najib Aziz, Lynn K Gordon, Jonathan Braun and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
2.0field-weighted citation impact, top 13% 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, 52 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. EMP3: A promising biomarker for tumor prognosis and targeted cancer therapy.Cancer biomarkers : section A of Disease markers · 2024
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. miR-340-5p mediates the therapeutic effect of mesenchymal stem cells on corneal neovascularization.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2022
    Article
  16. Article
  17. Article
  18. Characterization of microRNA Profiles inFrontiers in veterinary science · 2021
    Article
  19. Article
  20. 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

15 authors at 4 institutions in 2 countries.

Maoyong FuAuthors' Affiliations: Departments of Pathology and Laboratory Medicine, Surgery, Division of Surgical Oncology, Ophthalmology, and Microbiology, Immunology, and Molecular Genetics, and Jonsson Comprehensive Cancer Center, David Geffen School of Medicine at UCLA; Department of Surgery, Greater Los Angeles Veterans Affairs Healthcare System; Department of Pathology, Charles Drew University, Los Angeles, California; Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York, New York; and Institute of Experimental Biology and Medicine, University of Buenos Aires, Buenos Aires, Argentina.
Erin L Maresh
Gustavo F Helguera
Meagan Kiyohara
Yu Qin
Negin Ashki
Tracy R Daniels-Wells
Najib Aziz
Lynn K Gordon
Jonathan Braun
Yahya Elshimali
Robert A Soslow
Manuel L Penichet
Lee Goodglick
Madhuri Wadehra
University of Buenos Aires · ARVA Greater Los Angeles Healthcare System · USCharles R. Drew University of Medicine and Science · USMemorial Sloan Kettering Cancer Center · US

Funding

Women's CancersP30CA016042 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Samuel Wheeler French · 1985 to 2026
$134.5M
UCLA Clinical and Translational Science InstituteUL1TR000124 · NCATS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI DUBINETT, STEVEN M. · 2012 to 2015
$57.0M
Virology CoreP30AI028697 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CHEN, IRVIN S.Y. · 1991 to 2018
$39.9M
Supporting African American Churches to Promote Cancer ScreeningU54CA143931 · NCI · CHARLES R. DREW UNIVERSITY OF MED & SCI · PI VADGAMA, JAYDUTT V. · 2009 to 2022
$19.7M
Training and Mentoring ProgramsU54CA143930 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI PIETRAS, RICHARD JOSEPH · 2009 to 2020
$7.5M
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
Using EMP2 for Image Guided Drug Delivery for Breast CancerR01CA163971 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI OLAFSEN, TOVE, WADEHRA, MADHURI · 2012 to 2016
$1.6M
Antibody-mediated Gene Therapy for the Treatment of CancerK01CA138559 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI DANIELS-WELLS, TRACY RUTH · 2009 to 2013
$704k
NCATS NIH HHS UL1 TR000124NCATS NIH HHS UL1TR000124NCI NIH HHS K01 CA138559NCI NIH HHS K01-CA138559NCI NIH HHS NCI CA-86366NCI NIH HHS P30 CA016042NCI NIH HHS R01 CA163971NCI NIH HHS U24 CA086366NCI NIH HHS U54 CA143930NCI NIH HHS U54 CA143931NCI NIH HHS U54-CA-143931NIAID NIH HHS P30 AI028697
6 · The paper itself

Abstract

Despite significant advances in biology and medicine, the incidence and mortality due to breast cancer worldwide is still unacceptably high. Thus, there is an urgent need to discover new molecular targets. In this article, we show evidence for a novel target in human breast cancer, the tetraspan protein epithelial membrane protein-2 (EMP2). Using tissue tumor arrays, protein expression of EMP2 was measured and found to be minimal in normal mammary tissue, but it was upregulated in 63% of invasive breast cancer tumors and in 73% of triple-negative tumors tested. To test the hypothesis that EMP2 may be a suitable target for therapy, we constructed a fully human immunoglobulin G1 (IgG1) antibody specific for a conserved domain of human and murine EMP2. Treatment of breast cancer cells with the anti-EMP2 IgG1 significantly inhibited EMP2-mediated signaling, blocked FAK/Src signaling, inhibited invasion, and promoted apoptosis in vitro. In both human xenograft and syngeneic metastatic tumor monotherapy models, anti-EMP2 IgG1 retarded tumor growth without detectable systemic toxicity. This antitumor effect was, in part, attributable to a potent antibody-dependent cell-mediated cytotoxicity response as well as direct cytotoxicity induced by the monoclonal antibody. Together, these results identify EMP2 as a novel therapeutic target for invasive breast cancer.

Indexed as

AnimalsAntibodies, MonoclonalAntineoplastic AgentsBreast NeoplasmsCarcinoma, Ductal, BreastCell Line, TumorFemaleGene Expression Regulation, NeoplasticHumansLung NeoplasmsMammary Neoplasms, ExperimentalMembrane GlycoproteinsMiceMice, Inbred BALB CMolecular Targeted TherapySignal TransductionAntibodies, MonoclonalAntineoplastic AgentsEMP2 protein, humanMembrane Glycoproteins

Identifiers

PMID24448822
PMCPMC4034757
OpenAlexW2142331967

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.