Evidence map›Paper›PMID 9874797›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1999

Segregation of steroid receptor coactivator-1 from steroid receptors in mammary epithelium.

W S Shim, J DiRenzo, J A DeCaprio, R J Santen, M Brown, M H Jeng

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
7.4field-weighted citation impact, top 2% 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

19 citing papers in PubMed, 68 citations in OpenAlex.

  1. Article
  2. Article
  3. Overcoming Resistance to Endocrine Therapy in Breast Cancer: New Approaches to a Nagging Problem.Medical principles and practice : international journal of the Kuwait University, Health Science Centre · 2016
    Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Pubertal mammary gland development: insights from mouse models.Journal of mammary gland biology and neoplasia · 2006
    Review
  10. Review
  11. Supervillin associates with androgen receptor and modulates its transcriptional activity.Proceedings of the National Academy of Sciences of the United States of America · 2002
    Article
  12. Article
  13. Endogenously expressed estrogen receptor and coactivator AIB1 interact in MCF-7 human breast cancer cells.Proceedings of the National Academy of Sciences of the United States of America · 2000
    Article
  14. Review
  15. A reappraisal of progesterone action in the mammary gland.Journal of mammary gland biology and neoplasia · 2000
    Review
  16. Steroid receptor coactivator-1 (SRC-1) mediates the development of sex-specific brain morphology and behavior.Proceedings of the National Academy of Sciences of the United States of America · 2000
    Article
  17. Review
  18. Amplification and overexpression of peroxisome proliferator-activated receptor binding protein (PBP/PPARBP) gene in breast cancer.Proceedings of the National Academy of Sciences of the United States of America · 1999
    Article
  19. P/CAF associates with cyclin D1 and potentiates its activation of the estrogen receptor.Proceedings of the National Academy of Sciences of the United States of America · 1999
    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

6 authors at 2 institutions in 1 country.

W S ShimDepartment of Internal Medicine, Division of Hematology/Oncology, University of Virginia Health Sciences Center, Charlottesville, VA 22908, USA.
J DiRenzo
J A DeCaprio
R J Santen
M Brown
M H Jeng
Dana-Farber Cancer Institute · USHarvard University · US

Funding

FUNCTIONS OF ESTROGEN RECEPTOR ASSOCIATED PROTEINSR01CA057374 · NCI · DANA-FARBER CANCER INSTITUTE · PI BROWN, MYLES A · 1996 to 2001
$288k
NCI NIH HHS CA57374
6 · The paper itself

Abstract

Steroid receptor coactivator-1 (SRC-1) family members interact with steroid receptors, including estrogen receptor alpha (ERalpha) and progesterone receptor (PR), to enhance ligand-dependent transcription. However, the expression of ERalpha and SRC-1 was found to be segregated in distinct subsets of cells within the epithelium of the estrogen-responsive rat mammary gland. This finding was in contrast to the finding for the stroma, where significant numbers of cells coexpressed ERalpha and SRC-1. Treatment of animals with estrogen induced PR expression in the ERalpha-expressing mammary epithelial cells in the absence of detectable SRC-1 and did not affect the segregated pattern of SRC-1 and ERalpha expression. PR was neither expressed nor induced by estrogen treatment in stroma, despite the coexpression of ERalpha and SRC-1. These results suggest that SRC-1 is not necessary for ERalpha-mediated induction of PR in mammary epithelial cells and is also not sufficient for PR induction in stromal cells expressing both ERalpha and SRC-1. Furthermore, the expression of SRC-1 in a subpopulation of mammary epithelial cells distinct from those expressing ERalpha or PR raises the possibility that SRC-1 has cell type-specific functions other than simply to act as coactivator for ERalpha or PR in the mammary epithelium.

Indexed as

AnimalsEpithelial CellsEstrogensFemaleGene ExpressionHistone AcetyltransferasesImmunohistochemistryMammary Glands, AnimalNuclear Receptor Coactivator 1RatsRats, Sprague-DawleyReceptors, EstrogenReceptors, ProgesteroneReceptors, SteroidStromal CellsTranscription FactorsEstrogensHistone AcetyltransferasesNuclear Receptor Coactivator 1Receptors, EstrogenReceptors, ProgesteroneReceptors, SteroidTranscription Factors

Identifiers

PMID9874797
PMCPMC15118
OpenAlexW2117565990

What OpenQuestion holds

Textmetadata
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.