Evidence map›Paper›PMID 28492543›Full record

ArticleCell death & disease2017

BASP1 interacts with oestrogen receptor α and modifies the tamoxifen response.

Lindsey A Marsh, Samantha Carrera, Jayasha Shandilya, Kate J Heesom, Andrew D Davidson, Kathryn F Medler, Stefan Ge Roberts

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

23 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Reactivation of the silencedProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. A high-affinity cocaine binding site associated with the brain acid soluble protein 1.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  13. Article
  14. Cholesterol is required for transcriptional repression by BASP1.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  15. Identification of Basp1 as a novel angiogenesis-regulating gene by multi-model system studies.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Article
  16. Article
  17. Article
  18. 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

7 authors at 2 institutions in 2 countries.

Lindsey A MarshSchool of Cellular and Molecular Medicine, University of Bristol, Bristol, UK.
Samantha CarreraSchool of Cellular and Molecular Medicine, University of Bristol, Bristol, UK.
Jayasha ShandilyaDepartment of Biological Sciences, University at Buffalo, Buffalo, NY, USA.
Kate J HeesomProteomics Facility, Faculty of Biomedical Sciences, University of Bristol, Bristol, UK.
Andrew D DavidsonSchool of Cellular and Molecular Medicine, University of Bristol, Bristol, UK.
Kathryn F MedlerDepartment of Biological Sciences, University at Buffalo, Buffalo, NY, USA.
Stefan Ge RobertsSchool of Cellular and Molecular Medicine, University of Bristol, Bristol, UK.
University of Bristol · GBUniversity at Buffalo, State University of New York · US

Funding

Functional analysis of the WT1-BASP1 transcriptional repressor complexR01GM098609 · NIGMS · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI MEDLER, KATHRYN, ROBERTS, STEFAN · 2012 to 2015
$1.2M
Biotechnology and Biological Sciences Research Council BB/K000446/1Medical Research Council MR/K001027/1NIGMS NIH HHS R01 GM098609
6 · The paper itself

Abstract

Tamoxifen binds to oestrogen receptor α (ERα) to elicit distinct responses that vary by cell/tissue type and status, but the factors that determine these differential effects are unknown. Here we report that the transcriptional corepressor BASP1 interacts with ERα and in breast cancer cells, this interaction is enhanced by tamoxifen. We find that BASP1 acts as a major selectivity factor in the transcriptional response of breast cancer cells to tamoxifen. In all, 40% of the genes that are regulated by tamoxifen in breast cancer cells are BASP1 dependent, including several genes that are associated with tamoxifen resistance. BASP1 elicits tumour-suppressor activity in breast cancer cells and enhances the antitumourigenic effects of tamoxifen treatment. Moreover, BASP1 is expressed in breast cancer tissue and is associated with increased patient survival. Our data have identified BASP1 as an ERα cofactor that has a central role in the transcriptional and antitumourigenic effects of tamoxifen.

Indexed as

Breast NeoplasmsEstrogen Receptor alphaFemaleGene Expression Regulation, NeoplasticHumansK562 CellsMCF-7 CellsMembrane ProteinsNeoplasm ProteinsNerve Tissue ProteinsRepressor ProteinsTamoxifenTranscription, GeneticBASP1 protein, humanESR1 protein, humanEstrogen Receptor alphaMembrane ProteinsNeoplasm ProteinsNerve Tissue ProteinsRepressor ProteinsTamoxifen

Identifiers

PMID28492543
PMCPMC5520704
OpenAlexW2613581592

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.