Evidence map›Paper›PMID 23666965›Full record

ArticleThe Journal of clinical endocrinology and metabolism2013

Expression and function of the progesterone receptor in human prostate stroma provide novel insights to cell proliferation control.

Yue Yu, Liangliang Liu, Ning Xie, Hui Xue, Ladan Fazli, Ralph Buttyan, Yuzhuo Wang, Martin Gleave, Xuesen Dong

Abstract readComparative Study
In one paragraph

Article in The Journal of clinical endocrinology and metabolism, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
–field-weighted citation impact
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

30 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Systemic distribution of progesterone receptor subtypes in human tissues.The Journal of steroid biochemistry and molecular biology · 2020
    Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Androgen receptor targeted therapies in castration-resistant prostate cancer: Bench to clinic.International journal of urology : official journal of the Japanese Urological Association · 2016
    Review
  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

9 authors.

Yue YuVancouver Prostate Center, Department of Urologic Sciences, University of British Columbia, Vancouver, British Columbia, Canada V6H 3Z6.
Liangliang Liu
Ning Xie
Hui Xue
Ladan Fazli
Ralph Buttyan
Yuzhuo Wang
Martin Gleave
Xuesen Dong

Funding

TRANSCRIPTOME AND PROTEOME STRATIFICATION OF PROSTATE ADENOCARCINOMA PHENOTYPESP50CA097186 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI John Kyung Lee · 2002 to 2026
$58.1M
CIHR MOP-102904CIHR MOP-97934NCI NIH HHS P50 CA097186NCI NIH HHS P50CA097186
6 · The paper itself

Abstract

contextLike other tissues, the prostate is an admixture of many different cell types that can be segregated into components of the epithelium or stroma. Reciprocal interactions between these 2 types of cells are critical for maintaining prostate homeostasis, whereas aberrant stromal cell proliferation can disrupt this balance and result in diseases such as benign prostatic hyperplasia. Although the androgen and estrogen receptors are relatively well studied for their functions in controlling stromal cell proliferation and differentiation, the role of the progesterone receptor (PR) remains unclear.

objectiveThe aim of the study was to investigate the expression and function of the PR in the prostate. DESIGN AND

settingHuman prostate biopsies, renal capsule xenografts, and prostate stromal cells were used. Immunohistochemistry, Western blotting, real-time quantitative PCR, cell proliferation, flow cytometry, and gene microarray analyses were performed.

resultsTwo PR isoforms, PRA and PRB, are expressed in prostate stromal fibroblasts and smooth muscle cells, but not in epithelial cells. Both PR isoforms suppress prostate stromal cell proliferation through inhibition of the expression of cyclinA, cyclinB, and cdc25c, thus delaying cell cycling through S and M phases. Gene microarray analyses further demonstrated that PRA and PRB regulated different transcriptomes. However, one of the major gene groups commonly regulated by both PR isoforms was the one associated with regulation of cell proliferation.

conclusionPR plays an inhibitory role in prostate stromal cell proliferation.

Indexed as

Cell DivisionGene Expression Regulationcdc25 PhosphatasesCell Cycle ProteinsCell ProliferationCyclin ACyclin BEpithelial CellsGene Expression Regulation, NeoplasticHumansMaleMuscle, SmoothNeoplasm ProteinsOligonucleotide Array Sequence AnalysisProstateProstatic NeoplasmsCDC25C protein, humancdc25 PhosphatasesCell Cycle ProteinsCyclin ACyclin BNeoplasm Proteinsprogesterone receptor Aprogesterone receptor BProtein IsoformsReceptors, Progesterone

Identifiers

PMID23666965
PMCPMC4078099

What OpenQuestion holds

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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.