Evidence map›Paper›PMID 14973372›Full record

ReviewJournal of mammary gland biology and neoplasia2003

Expression profiling of human breast cancers and gene regulation by progesterone receptors.

Britta M Jacobsen, Jennifer K Richer, Carol A Sartorius, Kathryn B Horwitz

Abstract readReview
PubMed Publisher
In one paragraph

Review in Journal of mammary gland biology and neoplasia, 2003. 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
2.1field-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, 64 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Progesterone receptor isoform-specific promoter methylation: association of PRA promoter methylation with worse outcome in breast cancer patients.Clinical cancer research : an official journal of the American Association for Cancer Research · 2011
    Article
  13. Progesterone receptor action: defining a role in breast cancer.Expert review of endocrinology & metabolism · 2011
    Article
  14. Altered retinoid uptake and action contributes to cell survival in endometriosis.The Journal of clinical endocrinology and metabolism · 2010
    Article
  15. Progesterone receptor A-regulated gene expression in mammary organoid cultures.The Journal of steroid biochemistry and molecular biology · 2009
    Article
  16. Article
  17. Review
  18. Article
  19. Progesterone and breast cancer.Women's health (London, England) · 2008
    Review
  20. Review
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

4 authors at 2 institutions in 1 country.

Britta M JacobsenDepartment of Medicine, Division of Endocrinology, University of Colorado School of Medicine, Denver, Colorado 80262, USA. britta.jacobsen@uchsc.edu
Jennifer K Richer
Carol A Sartorius
Kathryn B Horwitz
University of Colorado Denver · USUniversity of Colorado Health · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Even the first expression profiling studies of breast cancers have generated new insights. They suggest for example, that information about tumor aggressiveness, prognosis, metastatic potential, or treatment outcome is encoded in, and can be deduced from, the primary tumor. On the other hand no clinical genomic array data have yet been published that deal with hormonal aspects of breast tumorigenesis, tumor progression, or therapeutics. Rather, studies have focused on experimental model systems. We review below the currently published data on array profiling in clinical breast cancer, then describe our studies in breast cancer cell lines and xenograft models dealing with progesterone receptors (PRs) and the role of progesterone. We demonstrate that the two PR isoforms, PR-A and PR-B, have mostly nonoverlapping molecular signatures when liganded by progesterone, with PR-B the more active form. Additionally, we document the surprising finding that unliganded PRs can regulate gene transcription, with PR-A the more active form. In ovariectomized mice supplemented with estradiol but lacking measurable progesterone, PR-B-expressing tumors grow to twice the size of PR-A-expressing ones. We conclude that in breast cancers, PRs are more than simple markers of estrogen receptor function. Rather, presence of PRs and the ratio of the two isoforms directly influence tumor phenotype, even in the absence of ligand.

Indexed as

Gene Expression ProfilingGene Expression Regulation, NeoplasticAnimalsBreast NeoplasmsFemaleHumansProgesteroneReceptors, ProgesteroneUterusProgesteroneReceptors, Progesterone

Identifiers

PMID14973372
OpenAlexW2025519084

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.