Evidence map›Paper›PMID 23073759›Full record

ReviewBreast cancer research and treatment2012

Role of epidermal growth factor receptor in breast cancer.

Hiroko Masuda, Dongwei Zhang, Chandra Bartholomeusz, Hiroyoshi Doihara, Gabriel N Hortobagyi, Naoto T Ueno

Abstract readReview
In one paragraph

Review in Breast cancer research and treatment, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 412 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
412citing papers in PubMed, 3 pooled it
11.5field-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

412 citing papers in PubMed, 3 syntheses or guidelines pooled it, 786 citations in OpenAlex.

  1. Pooled it
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  4. Trial
  5. Review
  6. Article
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  12. Unveiling the Pharmacological Potential ofInternational journal of molecular sciences · 2026
    Article
  13. Exploring the Role ofHealth science reports · 2026
    Article
  14. Article
  15. Review
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  17. Review
  18. Article
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352 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

6 authors at 2 institutions in 2 countries.

Hiroko MasudaDepartment of Breast Medical Oncology, Unit 1354, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Dongwei Zhang
Chandra Bartholomeusz
Hiroyoshi Doihara
Gabriel N Hortobagyi
Naoto T Ueno
The University of Texas MD Anderson Cancer Center · USOkayama University Hospital · JP

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Markers of sensivity to the EGFR inhibitor erlotinib in breast cancerR01CA123318 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI UENO, NAOTO T. · 2007 to 2012
$1.4M
NCI NIH HHS CA016672NCI NIH HHS P30 CA016672NCI NIH HHS R01 CA123318
6 · The paper itself

Abstract

Decades of research in molecular oncology have brought about promising new therapies which are designed to target specific molecules which promote tumor growth and survival. The epidermal growth factor receptor (EGFR) is one of the first identified important targets of these novel antitumor agents. Approximately half of cases of triple-negative breast cancer (TNBC) and inflammatory breast cancer (IBC) overexpress EGFR. Thus, EGFR inhibitors for treatment of breast cancer have been evaluated in several studies. However, results so far have been disappointing. One of the reasons for these unexpected results is the lack of biomarkers for predicting which patients are most likely to respond to EGFR inhibitors. Recent studies have shown that EGFR and its downstream pathway regulate epithelial-mesenchymal transition, migration, and tumor invasion and that high EGFR expression is an independent predictor of poor prognosis in IBC. Further, recent studies have shown that targeting EGFR enhances the chemosensitivity of TNBC cells by rewiring apoptotic signaling networks in TNBC. These studies indicate that EGFR-targeted therapy might have a promising role in TNBC and IBC. Further studies of the role of EGFR in TNBC and IBC are needed to better understand the best way to use EGFR-targeted therapy-e.g., as a chemosensitizer or to prevent metastases-to treat these aggressive diseases.

Indexed as

Antineoplastic AgentsBreast NeoplasmsClinical Trials as TopicEpithelial-Mesenchymal TransitionErb-b2 Receptor Tyrosine KinasesErbB ReceptorsFemaleHumansInflammatory Breast NeoplasmsMolecular Targeted TherapyNeoplasms, Basal CellProtein Kinase InhibitorsReceptors, EstrogenReceptors, ProgesteroneAntineoplastic AgentsErb-b2 Receptor Tyrosine KinasesErbB ReceptorsProtein Kinase InhibitorsReceptors, EstrogenReceptors, Progesterone

Identifiers

PMID23073759
PMCPMC3832208
OpenAlexW1988055795

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.