Evidence map›Paper›PMID 12118371›Full record

ArticleOncogene2002

Phosphorylation of human estrogen receptor alpha at serine 118 by two distinct signal transduction pathways revealed by phosphorylation-specific antisera.

Dongsheng Chen, Elinor Washbrook, Naveed Sarwar, Gaynor J Bates, Paul E Pace, Vatsala Thirunuvakkarasu, Jacqueline Taylor, Richard J Epstein, Frances V Fuller-Pace, Jean-Marc Egly and 2 more

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 93 papers.

0numbers the graph read from it
0cells of the map it votes in
93citing papers in PubMed
5.6field-weighted citation impact, top 4% 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

93 citing papers in PubMed, 239 citations in OpenAlex.

  1. Trial
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  10. Article
  11. Article
  12. Endocrine therapy resistance: what we know and future directions.Exploration of targeted anti-tumor therapy · 2022
    Review
  13. Estrogen Receptor Alpha and ESR1 Mutations in Breast Cancer.Advances in experimental medicine and biology · 2022
    Article
  14. Article
  15. Thyroid hormone receptor phosphorylation regulates acute fasting-induced suppression of the hypothalamic-pituitary-thyroid axis.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  16. Article
  17. Article
  18. CDK7 inhibitors as anticancer drugs.Cancer metastasis reviews · 2020
    Review
  19. Article
  20. Article

33 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

12 authors at 5 institutions in 2 countries.

Dongsheng ChenDepartment of Cancer Medicine, Imperial College of Science, Technology and Medicine, Hammersmith Hospital Campus, Du Cane Road, London W12 0NN, UK.
Elinor Washbrook
Naveed Sarwar
Gaynor J Bates
Paul E Pace
Vatsala Thirunuvakkarasu
Jacqueline Taylor
Richard J Epstein
Frances V Fuller-Pace
Jean-Marc Egly
R Charles Coombes
Simak Ali
Hammersmith Hospital · GBImperial College London · GBInstitut de génétique et de biologie moléculaire et cellulaire · FRNinewells Hospital · GBUniversity of Dundee · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Estrogen receptor alpha (ERalpha) is a transcription factor that regulates expression of target genes in a ligand-dependent manner. Activation of gene expression is mediated by two transcription activation functions AF-1 and AF-2, which act in a promoter- and cell-specific manner. Whilst AF-2 activity is regulated by estrogen (E2) binding, the activity of AF-1 is additionally modulated by phosphorylation at several sites. One of these phosphorylation sites, serine 118 (S118) is of particular interest as its mutation significantly reduces ERalpha activity. Previous studies have shown that S118 can be phosphorylated by the ERK1/2 mitogen activated protein kinases (MAPK) and by the cyclin-dependent protein kinase Cdk7. In this study we use antisera that specifically recognize ERalpha phosphorylated at S118 to demonstrate that MAPK phosphorylates S118 in a ligand-independent manner, whereas Cdk7 mediates E2-induced phosphorylation of S118. E2 stimulation of S118 phosphorylation was observed within 10 min of its addition and was maximal at 10(-7) M E2. S118 phosphorylation was maximal at 30 min but then declined, such that by 180 min following E2 addition little S118 phosphorylation was evident. S118 phosphorylation was also induced by the partial estrogen antagonist 4-hydroxytamoxifen, but not by the complete antagonist ICI 182, 780. S118 phosphorylation upon addition of the MAPK inducers EGF or PMA followed the expected time courses. Finally, we show that ERalpha is phosphorylated at S118 in vivo using immunoblotting of extracts prepared from a series of ERalpha-positive breast tumours.

Indexed as

Cyclin-Dependent KinasesSerineSignal TransductionAmino Acid SequenceAnimalsAntibodiesBreast NeoplasmsCOS CellsCyclin-Dependent Kinase-Activating KinaseEstradiolEstrogen AntagonistsEstrogen Receptor alphaEstrogensFulvestrantHumansMitogen-Activated Protein KinasesafimoxifeneAntibodiesCDK7 protein, humanCyclin-Dependent Kinase-Activating KinaseCyclin-Dependent KinasesEstradiolEstrogen AntagonistsEstrogen Receptor alphaEstrogensFulvestrantMitogen-Activated Protein KinasesProtein Serine-Threonine KinasesReceptors, EstrogenSerineTamoxifen

Identifiers

PMID12118371
OpenAlexW1970755773

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.