Evidence map›Paper›PMID 26542058›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2016

ERRα Is a Marker of Tamoxifen Response and Survival in Triple-Negative Breast Cancer.

Subrata Manna, Josefine Bostner, Yang Sun, Lance D Miller, Anya Alayev, Naomi S Schwartz, Elin Lager, Tommy Fornander, Bo Nordenskjöld, Jane J Yu and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2016. 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
4.0field-weighted citation impact, top 6% 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, 56 citations in OpenAlex.

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  13. Triple-negative breast lobular carcinoma: a luminal androgen receptor carcinoma with specific ESRRA mutations.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2021
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  18. Unraveling the multifaceted nature of the nuclear function of mTOR.Biochimica et biophysica acta. Molecular cell research · 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

12 authors at 1 institution in 1 country.

Subrata MannaDepartment of Biology; Stern College for Women of Yeshiva University; New York, New York.
Josefine BostnerDepartment of Clinical and Experimental Medicine, and Department of Oncology, Linköping University, Linköping, Sweden.
Yang SunDivision of Pulmonary and Critical Care, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Lance D MillerDepartment of Cancer Biology, Wake Forest School of Medicine, Winston-Salem, North Carolina. The Comprehensive Cancer Center of Wake Forest University, Winston Salem, North Carolina.
Anya AlayevDepartment of Biology; Stern College for Women of Yeshiva University; New York, New York.
Naomi S SchwartzDepartment of Biology; Stern College for Women of Yeshiva University; New York, New York.
Elin LagerDepartment of Clinical and Experimental Medicine, and Department of Oncology, Linköping University, Linköping, Sweden.
Tommy FornanderDepartment of Oncology, Karolinska University Hospital, Stockholm South General Hospital, Karolinska Institute, Stockholm, Sweden.
Bo NordenskjöldDepartment of Clinical and Experimental Medicine, and Department of Oncology, Linköping University, Linköping, Sweden.
Jane J YuDivision of Pulmonary and Critical Care, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Olle StålDepartment of Clinical and Experimental Medicine, and Department of Oncology, Linköping University, Linköping, Sweden.
Marina K HolzDepartment of Biology; Stern College for Women of Yeshiva University; New York, New York. Department of Molecular Pharmacology, Albert Einstein College of Medicine, New York, New York. Albert Einstein Cancer Center; Albert Einstein College of Medicine; Bronx, New York. mholz@yu.edu.
The Bronx Defenders · US

Funding

Targeting the Estrogen Pathway for the Prevention and Treatment of LAMR01HL098216 · NHLBI · UNIVERSITY OF CINCINNATI · PI YU, JANE · 2010 to 2014
$2.1M
The role of the mTOR signaling pathway in ER-positive breast cancerR15CA151112 · NCI · YESHIVA UNIVERSITY · PI HOLZ, MARINA K · 2010 to 2013
$951k
Prostaglandin biosynthesis: a novel therapeutic target in TSC disordersR01DK098331 · NIDDK · UNIVERSITY OF CINCINNATI · PI YU, JANE · 2014 to 2016
$739k
NCI NIH HHS CA151112NCI NIH HHS R15 CA151112NHLBI NIH HHS HL098216NHLBI NIH HHS R01 HL098216NIDDK NIH HHS R01 DK098331
6 · The paper itself

Abstract

purposeEstrogen-related receptor alpha (ERRα) signaling has recently been implicated in breast cancer. We investigated the clinical value of ERRα in randomized cohorts of tamoxifen-treated and adjuvant-untreated patients. EXPERIMENTAL

designCox proportional hazards regression was used to evaluate the significance of associations between ERRα gene expression levels and patient DMFS in a previously published microarray dataset representing 2,000 breast tumor cases derived from multiple medical centers worldwide. The 912 tumors used for immunostaining were from a tamoxifen-randomized primary breast cancer trial conducted in Stockholm, Sweden, during 1976-1990. Mouse model was used to study the effect of tamoxifen treatment on lung colonization of MDA-MB-231 control cells and MDA-MB-231 cells with stable knockdown of ERRα. The phenotypic effects associated with ERRα modulation were studied using immunoblotting analyses and wound-healing assay.

resultsWe found that in ER-negative and triple-negative breast cancer (TNBC) adjuvant-untreated patients, ERRα expression indicated worse prognosis and correlated with poor outcome predictors. However, in tamoxifen-treated patients, an improved outcome was observed with high ERRα gene and protein expression. Reduced ERRα expression was oncogenic in the presence of tamoxifen, measured by in vitro proliferation and migration assays and in vivo metastasis studies.

conclusionsTaken together, these data show that ERRα expression predicts response to tamoxifen treatment, and ERRα could be a biomarker of tamoxifen sensitivity and a prognostic factor in TNBC.

Indexed as

Biomarkers, TumorAntineoplastic Agents, HormonalCell Line, TumorERRalpha Estrogen-Related ReceptorFemaleGene ExpressionGene Knockout TechniquesHumansNeoplasm GradingPrognosisProtein TransportReceptors, EstrogenRNA, Small InterferingTamoxifenTreatment OutcomeTriple Negative Breast NeoplasmsAntineoplastic Agents, HormonalBiomarkers, TumorERRalpha Estrogen-Related ReceptorReceptors, EstrogenRNA, Small InterferingTamoxifen

Identifiers

PMID26542058
PMCPMC4794381
OpenAlexW2132876740

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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.