Evidence map›Paper›PMID 19904813›Full record

ReviewBioFactors (Oxford, England)

Steroid receptor phosphorylation: Assigning function to site-specific phosphorylation.

Robert D Ward, Nancy L Weigel

Abstract readReview
In one paragraph

Review in BioFactors (Oxford, England). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing 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

44 citing papers in PubMed.

  1. Article
  2. Intact Mass Proteomics Using a Proteoform Atlas.Journal of proteome research · 2025
    Article
  3. Article
  4. Demystifying the Functional Role of Nuclear Receptors in Esophageal Cancer.International journal of molecular sciences · 2022
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Development of selective androgen receptor modulators (SARMs).Molecular and cellular endocrinology · 2018
    Review
  11. Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Post-translational modifications of the progesterone receptors.The Journal of steroid biochemistry and molecular biology · 2014
    Review
  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

2 authors.

Robert D WardDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030, USA.
Nancy L Weigel

Funding

REGULATION OF HUMAN STEROID RECEPTORS BY PHOSPHORYLATIONR01CA057539 · NCI · BAYLOR COLLEGE OF MEDICINE · PI WEIGEL, NANCY L. · 1993 to 2010
$4.0M
The Role of Progesterone Receptor Phosphorylation in Target Gene RegulationF32CA130430 · NCI · BAYLOR COLLEGE OF MEDICINE · PI WARD, ROBERT DARYL · 2007 to 2008
$96k
NCI NIH HHS F32 CA130430NCI NIH HHS R01 CA057539NCI NIH HHS R01 CA57539
6 · The paper itself

Abstract

Steroid receptors (SRs) are hormone-activated transcription factors important for a wide variety of cellular functions. Post-translational modifications of SRs, including phosphorylation, ubiquitination, acetylation, and sumoylation regulate their expression and function. The remarkable number of phosphorylation sites in these receptors and the wide variety of kinases shown to modulate phosphorylation influence the integration between cell-signaling pathways and SR action. These phosphorylation sites have been identified in all of the functional domains with the majority being located within the amino-terminal portions of the receptors. The regulation of function is receptor specific, site specific, and often dependent on the cellular context. Numerous roles for site-specific phosphorylation have been elucidated including sensitivity of hormone response, DNA binding, expression, stability, subcellular localization, dimerization, and protein-protein interactions that can determine the regulation of specific target genes. This review summarizes the current knowledge regarding receptor site-specific phosphorylation and regulation of function. As functional assays become more sophisticated, it is likely that additional roles for phosphorylation in receptor function will be identified.

Indexed as

AnimalsHumansModels, BiologicalPhosphorylationReceptors, AndrogenReceptors, EstrogenReceptors, GlucocorticoidReceptors, ProgesteroneReceptors, SteroidReceptors, AndrogenReceptors, EstrogenReceptors, GlucocorticoidReceptors, ProgesteroneReceptors, Steroid

Identifiers

PMID19904813
PMCPMC2788675

What OpenQuestion holds

Textmetadata
LicenceTDM
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.