Evidence map›Paper›PMID 29644001›Full record

ArticleOncotarget2018

BAG3 promotes tumour cell proliferation by regulating EGFR signal transduction pathways in triple negative breast cancer.

Sarah Shields, Emer Conroy, Tony O'Grady, Alo McGoldrick, Kate Connor, Mark P Ward, Zivile Useckaite, Eugene Dempsey, Rebecca Reilly, Yue Fan and 7 more

Erratum issuedOpen access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.7field-weighted citation impact, top 27% 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

17 citing papers in PubMed, 22 citations in OpenAlex.

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  7. Skeletal Muscle-SpecificInternational journal of molecular sciences · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 3 institutions in 1 country.

Sarah ShieldsUCD School of Biomolecular and Biomedical Science, University College Dublin, Dublin 4, Ireland.
Emer ConroyUCD School of Biomolecular and Biomedical Science, University College Dublin, Dublin 4, Ireland.
Tony O'GradyRoyal College of Surgeons in Ireland, Beaumont Hospital, Dublin 9, Ireland.
Alo McGoldrickUCD School of Biomolecular and Biomedical Science, University College Dublin, Dublin 4, Ireland.
Kate ConnorRoyal College of Surgeons in Ireland, Dublin 2, Ireland.
Mark P WardRoyal College of Surgeons in Ireland, Dublin 2, Ireland.
Zivile UseckaiteRoyal College of Surgeons in Ireland, Dublin 2, Ireland.
Eugene DempseySchool of Biology and Environmental Science, University College Dublin, Dublin 4, Ireland.
Rebecca ReillyUCD School of Biomolecular and Biomedical Science, University College Dublin, Dublin 4, Ireland.
Yue FanUCD School of Biomolecular and Biomedical Science, University College Dublin, Dublin 4, Ireland.
Anthony ChubbRoyal College of Surgeons in Ireland, Dublin 2, Ireland.
David Gomez MatallanasUCD School of Medicine, University College Dublin, Dublin 4, Ireland.
Elaine W KayRoyal College of Surgeons in Ireland, Beaumont Hospital, Dublin 9, Ireland.
Darran O'ConnorRoyal College of Surgeons in Ireland, Dublin 2, Ireland.
Amanda McCannUCD School of Biomolecular and Biomedical Science, University College Dublin, Dublin 4, Ireland.
William M GallagherUCD School of Biomolecular and Biomedical Science, University College Dublin, Dublin 4, Ireland.
Judith A CoppingerUCD School of Biomolecular and Biomedical Science, University College Dublin, Dublin 4, Ireland.
University College Dublin · IERoyal College of Surgeons in Ireland · IEBeaumont Hospital · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Triple-negative breast cancer (TNBC), is a heterogeneous disease characterised by absence of expression of the estrogen receptor (ER), progesterone receptor (PR) and lack of amplification of human epidermal growth factor receptor 2 (HER2). TNBC patients can exhibit poor prognosis and high recurrence stages despite early response to chemotherapy treatment. In this study, we identified a pro-survival signalling protein BCL2- associated athanogene 3 (BAG3) to be highly expressed in a subset of TNBC cell lines and tumour tissues. High mRNA expression of BAG3 in TNBC patient cohorts significantly associated with a lower recurrence free survival. The epidermal growth factor receptor (EGFR) is amplified in TNBC and EGFR signalling dynamics impinge on cancer cell survival and disease recurrence. We found a correlation between BAG3 and EGFR expression in TNBC cell lines and determined that BAG3 can regulate tumour cell proliferation, migration and invasion in EGFR expressing TNBC cells lines. We identified an interaction between BAG3 and components of the EGFR signalling networks using mass spectrometry. Furthermore, BAG3 contributed to regulation of proliferation in TNBC cell lines by reducing the activation of components of the PI3K/AKT and FAK/Src signalling subnetworks. Finally, we found that combined targeting of BAG3 and EGFR was more effective than inhibition of EGFR with Cetuximab alone in TNBC cell lines. This study demonstrates a role for BAG3 in regulation of distinct EGFR modules and highlights the potential of BAG3 as a therapeutic target in TNBC.

Indexed as

BAG3EGFRproliferationsignallingTNBC

Identifiers

PMID29644001
PMCPMC5884656
OpenAlexW2793091091

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.