Evidence map›Paper›PMID 2328727›Full record

ArticleThe EMBO journal1990

Two distinct estrogen-regulated promoters generate transcripts encoding the two functionally different human progesterone receptor forms A and B.

P Kastner, A Krust, B Turcotte, U Stropp, L Tora, H Gronemeyer, P Chambon

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in The EMBO journal, 1990. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02651844 (Mifepristone Treatment for Breast Cancer Patients Expressing Levels of Progesterone Receptor Isoform A), which is not on this map. Cited by 416 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
416citing papers in PubMed, 5 pooled it
19.8field-weighted citation impact, top 1% 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.

NCT02651844 nacompletednot on this mapstarted 2016, after this paper: background citation

Mifepristone Treatment for Breast Cancer Patients Expressing Levels of Progesterone Receptor Isoform A (PRA) Higher Than Those of Isoform B (PRB): Neoadjuvant Therapy.

TypeinterventionalSponsorHospital Provincial Magdalena V. de MartínezRan2016 to 2019Enrolled20ConditionsBreast CancerArmsMifepristone
3 · Its place in the literature

Who cites it

416 citing papers in PubMed, 5 syntheses or guidelines pooled it, 1,543 citations in OpenAlex.

  1. Pooled it
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  5. Pooled it
  6. Trial
  7. Article
  8. Review
  9. Role of DCAF8 in Mammary Ductal Elongation and Branching Morphogenesis.Journal of mammary gland biology and neoplasia · 2026
    Article
  10. Review
  11. Review
  12. Review
  13. TGFBR2 coordinates the endometrial response to estrogen, regulating endometrial hyperplasia and fertility.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Review

356 more citing papers are in PubMed but not listed here.

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 1 country.

P KastnerLaboratoire de Génétique Moléculaire des Eucaryotes, CNRS, Strasbourg, France.
A Krust
B Turcotte
U Stropp
L Tora
H Gronemeyer
P Chambon
Centre National de la Recherche Scientifique · FRLaboratoire de Biologie Moléculaire et Cellulaire des Eucaryotes · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The human progesterone receptor (hPR) cDNA, synthesized from T47D breast cancer cells, and the hPR gene 5'-flanking region were cloned and sequenced. Comparison of the cDNA-deduced amino acid sequence with other PR homologues demonstrated the modular structure characteristic of nuclear receptors. As in the case of the chicken homologue, there are two hPR forms, A and B, which originate from translational initiation at AUG2 (codon 165) and AUG1, respectively. Northern blot analysis of T47D mRNA using various cDNA derived probes identified two classes of hPR mRNAs, one of which could code for hPR form B, while the other one lacked the 5' region upstream of AUG1. S1 nuclease mapping and primer extension analyses confirmed that the second class of hPR transcripts are initiated between +737 and +842 and thus encode hPR form A, but not form B. By using the hPR gene 5'-flanking sequences as promoter region in chimeric genes, we show that a functional promoter (located between -711 and +31) directs initiation of hPR mRNAs from the authentic start sites located at +1 and +15. Most importantly, initiation of transcription from chimeric genes demonstrated the existence of a second promoter located between +464 and +1105. Transient co-transfection experiments with vectors expressing the human estrogen receptor showed that both promoters were estrogen inducible, although no classical estrogen responsive element was detected in the corresponding sequences. When transiently expressed, the two hPR forms similarly activated transcription from reporter genes containing a single palindromic progestin responsive element (PRE), while form B was more efficient at activating the PRE of the mouse mammary tumor virus long terminal repeat. Transcription from the ovalbumin promoter, however, was induced by hPR form A, but not by form B.

Indexed as

Amino Acid SequenceBase SequenceCloning, MolecularEstrogensGene Expression RegulationHumansMolecular Sequence DataPromoter Regions, GeneticReceptors, ProgesteroneRegulatory Sequences, Nucleic AcidRNA, MessengerTranscription, GeneticEstrogensReceptors, ProgesteroneRNA, Messenger

Identifiers

PMID2328727
PMCPMC551856
OpenAlexW1569704074

What OpenQuestion holds

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Read underepoch 390

Registered trials

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.