Evidence map›Paper›PMID 22362749›Full record

ArticleNucleic acids research2012

Retinoic acid and androgen receptors combine to achieve tissue specific control of human prostatic transglutaminase expression: a novel regulatory network with broader significance.

Guillermo C Rivera-Gonzalez, Alastair P Droop, Helen J Rippon, Katrin Tiemann, Davide Pellacani, Lindsay J Georgopoulos, Norman J Maitland

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

20 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Biochemical Characterisation of Human Transglutaminase 4.International journal of molecular sciences · 2021
    Article
  6. TGM4: an immunogenic prostate-restricted antigen.Journal for immunotherapy of cancer · 2021
    Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Biological functional annotation of retinoic acid alpha and beta in mouse liver based on genome-wide binding.American journal of physiology. Gastrointestinal and liver physiology · 2014
    Article
  15. Article
  16. Article
  17. Article
  18. Review
  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 1 country.

Guillermo C Rivera-GonzalezDepartment of Biology, Yorkshire Cancer Research Unit, University of York, Heslington, York YO10 5DD, UK.
Alastair P Droop
Helen J Rippon
Katrin Tiemann
Davide Pellacani
Lindsay J Georgopoulos
Norman J Maitland
University of York · GBYorkshire Cancer Research · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the human prostate, expression of prostate-specific genes is known to be directly regulated by the androgen-induced stimulation of the androgen receptor (AR). However, less is known about the expression control of the prostate-restricted TGM4 (hTGP) gene. In the present study we demonstrate that the regulation of the hTGP gene depends mainly on retinoic acid (RA). We provide evidence that the retinoic acid receptor gamma (RAR-G) plays a major role in the regulation of the hTGP gene and that presence of the AR, but not its transcriptional transactivation activity, is critical for hTGP transcription. RA and androgen responsive elements (RARE and ARE) were mapped to the hTGP promoter by chromatin immunoprecipitation (ChIP), which also indicated that the active ARE and RARE sites were adjacent, suggesting that the antagonistic effect of androgen and RA is related to the relative position of binding sites. Publicly available AR and RAR ChIP-seq data was used to find gene potentially regulated by AR and RAR. Four of these genes (CDCA7L, CDK6, BTG1 and SAMD3) were tested for RAR and AR binding and two of them (CDCA7L and CDK6) proved to be antagonistically regulated by androgens and RA confirming that this regulation is not particular of hTGP.

Indexed as

Gene Expression Regulation, EnzymologicGene Regulatory NetworksAndrogensCell Line, TumorEnhancer Elements, GeneticHumansMaleMetribolonePromoter Regions, GeneticProstateProstatic NeoplasmsReceptors, AndrogenReceptors, Retinoic AcidRetinoic Acid Receptor gammaTranscriptional ActivationTransglutaminasesAndrogensMetriboloneReceptors, AndrogenReceptors, Retinoic AcidRetinoic Acid Receptor gammatransglutaminase 4TransglutaminasesTretinoin

Identifiers

PMID22362749
PMCPMC3367184
OpenAlexW2143342123

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.