Evidence map›Paper›PMID 29192207›Full record

ArticleNature communications2017

Discovery of naturally occurring ESR1 mutations in breast cancer cell lines modelling endocrine resistance.

Lesley-Ann Martin, Ricardo Ribas, Nikiana Simigdala, Eugene Schuster, Sunil Pancholi, Tencho Tenev, Pascal Gellert, Laki Buluwela, Alison Harrod, Allan Thornhill and 18 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 96 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
96citing papers in PubMed, 1 pooled it
13.9field-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

96 citing papers in PubMed, 1 synthesis or guideline pooled it, 155 citations in OpenAlex.

  1. Pooled it
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  14. TRIM24 as a therapeutic target in endocrine treatment-resistant breast cancer.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
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36 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

28 authors at 6 institutions in 3 countries.

Lesley-Ann MartinBreast Cancer Now Toby Robins Research Centre, Institute of Cancer Research, London, SW7 3RP, UK. Lesley-ann.martin@icr.ac.uk.
Ricardo RibasBreast Cancer Now Toby Robins Research Centre, Institute of Cancer Research, London, SW7 3RP, UK.
Nikiana SimigdalaBreast Cancer Now Toby Robins Research Centre, Institute of Cancer Research, London, SW7 3RP, UK.
Eugene SchusterBreast Cancer Now Toby Robins Research Centre, Institute of Cancer Research, London, SW7 3RP, UK.
Sunil PancholiBreast Cancer Now Toby Robins Research Centre, Institute of Cancer Research, London, SW7 3RP, UK.
Tencho TenevBreast Cancer Now Toby Robins Research Centre, Institute of Cancer Research, London, SW7 3RP, UK.
Pascal GellertBreast Cancer Now Toby Robins Research Centre, Institute of Cancer Research, London, SW7 3RP, UK.
Laki BuluwelaDivision of Cancer, CRUK Labs, University of London Imperial College, London, W12 0NN, UK.
Alison HarrodDivision of Cancer, CRUK Labs, University of London Imperial College, London, W12 0NN, UK.
Allan ThornhillCentre for Cancer Imaging, Institute of Cancer Research, Sutton, SM2 5NG, UK.
Joanna Nikitorowicz-BuniakBreast Cancer Now Toby Robins Research Centre, Institute of Cancer Research, London, SW7 3RP, UK.
Amandeep BhamraProteomic Unit, Institute of Cancer Research, London, SW7 3RP, UK.
Marc-Olivier TurgeonDivision of Cancer Biology, The Institute of Cancer Research, London, SW3 6JB, UK.
George PoulogiannisDivision of Cancer Biology, The Institute of Cancer Research, London, SW3 6JB, UK.
Qiong GaoBreast Cancer Now Toby Robins Research Centre, Institute of Cancer Research, London, SW7 3RP, UK.
Vera MartinsRalph Lauren Centre for Breast Cancer Research, Royal Marsden Hospital, London, SW3 6JB, UK.
Margaret HillsRalph Lauren Centre for Breast Cancer Research, Royal Marsden Hospital, London, SW3 6JB, UK.
Isaac Garcia-MurillasBreast Cancer Now Toby Robins Research Centre, Institute of Cancer Research, London, SW7 3RP, UK.
Charlotte FribbensBreast Cancer Now Toby Robins Research Centre, Institute of Cancer Research, London, SW7 3RP, UK.
Neill PataniBreast Cancer Now Toby Robins Research Centre, Institute of Cancer Research, London, SW7 3RP, UK.
Zheqi LiDepartment of Pharmacology and Chemical biology, University of Pittsburgh, Pittsburgh, PA, 15213, USA.
Matthew J SikoraDepartment of Pharmacology and Chemical biology, University of Pittsburgh, Pittsburgh, PA, 15213, USA.
Nicholas TurnerBreast Cancer Now Toby Robins Research Centre, Institute of Cancer Research, London, SW7 3RP, UK.
Wilbert ZwartDepartment of Molecular Pathology, Netherlands Cancer Institute, 1066CX, Amsterdam, Netherlands.
Steffi OesterreichDepartment of Pharmacology and Chemical biology, University of Pittsburgh, Pittsburgh, PA, 15213, USA.ORCID http://orcid.org/0000-0002-2537-6923
Jason CarrollCancer Research UK Cambridge Institute, University of Cambridge, Cambridge, CB2 0RE, UK.
Simak AliDivision of Cancer, CRUK Labs, University of London Imperial College, London, W12 0NN, UK.ORCID http://orcid.org/0000-0002-1320-0816
Mitch DowsettBreast Cancer Now Toby Robins Research Centre, Institute of Cancer Research, London, SW7 3RP, UK.
Institute of Cancer Research · GBUniversity of London · GBUniversity of Pittsburgh · USRoyal Marsden Hospital · GBThe Netherlands Cancer Institute · NLUniversity of Cambridge · GB

Funding

Cancer Research UK 12011Cancer Research UK 18784Cancer Research UK 20411Cancer Research UK C37/A18784Medical Research Council G1100450Wellcome TrustWellcome Trust 090532/Z/09/Z
6 · The paper itself

Abstract

Resistance to endocrine therapy remains a major clinical problem in breast cancer. Genetic studies highlight the potential role of estrogen receptor-α (ESR1) mutations, which show increased prevalence in the metastatic, endocrine-resistant setting. No naturally occurring ESR1 mutations have been reported in in vitro models of BC either before or after the acquisition of endocrine resistance making functional consequences difficult to study. We report the first discovery of naturally occurring ESR1

Indexed as

Breast NeoplasmsCell Line, TumorDrug Resistance, NeoplasmEstradiolEstrogen Receptor alphaEstrogen Receptor AntagonistsFemaleFulvestrantHumansMCF-7 CellsMutationSelective Estrogen Receptor ModulatorsTamoxifenESR1 protein, humanEstradiolEstrogen Receptor alphaEstrogen Receptor AntagonistsFulvestrantSelective Estrogen Receptor ModulatorsTamoxifen

Identifiers

PMID29192207
PMCPMC5709387
OpenAlexW2765643657

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.