Evidence map›Paper›PMID 26527289›Full record

ArticleCancer research2015

Amphiregulin Is a Critical Downstream Effector of Estrogen Signaling in ERα-Positive Breast Cancer.

Esther A Peterson, Edmund C Jenkins, Kristopher A Lofgren, Natasha Chandiramani, Hui Liu, Evelyn Aranda, Maryia Barnett, Paraic A Kenny

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

31 citing papers in PubMed, 61 citations in OpenAlex.

  1. Trial
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  4. Roles and signaling pathways of CITED1 in tumors: overview and novel insights.The Journal of international medical research · 2024
    Review
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  18. Inter-Individual Variation in Response to Estrogen in Human Breast Explants.Journal of mammary gland biology and neoplasia · 2020
    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

8 authors at 2 institutions in 1 country.

Esther A PetersonDepartment of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, New York.
Edmund C JenkinsDepartment of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, New York.
Kristopher A LofgrenDepartment of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, New York. Oncology Research Laboratory, Kabara Cancer Research Institute, Gundersen Medical Foundation, La Crosse, Wisconsin.
Natasha ChandiramaniDepartment of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, New York.
Hui LiuDepartment of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, New York.
Evelyn ArandaDepartment of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, New York.
Maryia BarnettDepartment of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, New York.
Paraic A KennyDepartment of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, New York. Oncology Research Laboratory, Kabara Cancer Research Institute, Gundersen Medical Foundation, La Crosse, Wisconsin. paraic@kennylab.org.
Albert Einstein College of Medicine · USGundersen Health System · US

Funding

WORD PROCESSORP30CA013330 · NCI · YESHIVA UNIVERSITY · PI THOMAS E ROHAN · 1985 to 2026
$111.2M
Bronx-Einstein Training in Teaching and Research (BETTR), an IRACDA programK12GM102779 · NIGMS · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI Dianne Cox, Johanna Patricia Daily · 2012 to 2026
$9.2M
NCI NIH HHS P30 CA013330NIGMS NIH HHS 1K12GM102779-01NIGMS NIH HHS K12 GM102779
6 · The paper itself

Abstract

Estrogen stimulation promotes epithelial cell proliferation in estrogen receptor (ERα)-positive breast cancer. Many ERα target genes have been enumerated, but the identities of the key effectors mediating the estrogen signal remain obscure. During mouse mammary gland development, the estrogen growth factor receptor (EGFR) ligand amphiregulin acts as an important stage-specific effector of estrogen signaling. In this study, we investigated the role of amphiregulin in breast cancer cell proliferation using human tissue samples and tumor xenografts in mice. Amphiregulin was enriched in ERα-positive human breast tumor cells and required for estrogen-dependent growth of MCF7 tumor xenografts. Furthermore, amphiregulin levels were suppressed in patients treated with endocrine therapy. Suppression of EGF receptor signaling appeared necessary for the therapeutic response in this setting. Our findings implicate amphiregulin as a critical mediator of the estrogen response in ERα-positive breast cancer, emphasizing the importance of EGF receptor signaling in breast tumor pathogenesis and therapeutic response.

Indexed as

AmphiregulinAnimalsBreast NeoplasmsCell Line, TumorEGF Family of ProteinsEnzyme-Linked Immunosorbent AssayEstrogen Receptor alphaEstrogensFemaleHeterograftsHumansImmunohistochemistryMiceReverse Transcriptase Polymerase Chain ReactionSignal TransductionTissue Array AnalysisAmphiregulinAREG protein, humanEGF Family of ProteinsESR1 protein, humanEstrogen Receptor alphaEstrogens

Identifiers

PMID26527289
PMCPMC4651747
OpenAlexW1942186358

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.