Evidence map›Paper›PMID 32358577›Full record

ArticleProstate cancer and prostatic diseases2020

Androgen receptor phosphorylation at serine 81 and serine 213 in castrate-resistant prostate cancer.

Milly J McAllister, Pamela McCall, Ashley Dickson, Mark A Underwood, Ditte Andersen, Elizabeth Holmes, Elke Markert, Hing Y Leung, Joanne Edwards

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Prostate cancer and prostatic diseases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

13 citing papers in PubMed, 14 citations in OpenAlex.

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  12. The Impact ofInternational journal of environmental research and public health · 2020
    Article
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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 at 4 institutions in 1 country.

Milly J McAllisterUnit of Gastrointestinal Cancer and Molecular Pathology, Institute of Cancer Sciences, College of Medical, Veterinary, and Life Sciences, University of Glasgow, Glasgow, G61 1QH, UK. m.mcallister.1@research.gla.ac.uk.ORCID http://orcid.org/0000-0003-4952-8255
Pamela McCallUnit of Gastrointestinal Cancer and Molecular Pathology, Institute of Cancer Sciences, College of Medical, Veterinary, and Life Sciences, University of Glasgow, Glasgow, G61 1QH, UK.
Ashley DicksonUnit of Gastrointestinal Cancer and Molecular Pathology, Institute of Cancer Sciences, College of Medical, Veterinary, and Life Sciences, University of Glasgow, Glasgow, G61 1QH, UK.
Mark A UnderwoodDepartment of Urology, Queen Elizabeth University Hospital, Glasgow, G31 2ER, UK.
Ditte AndersenBioClavis Ltd, Glasgow, G51 4TF, UK.
Elizabeth HolmesBioClavis Ltd, Glasgow, G51 4TF, UK.
Elke MarkertCancer Research UK Beatson Institute, Glasgow, G61 1BD, UK.
Hing Y LeungUnit of Gastrointestinal Cancer and Molecular Pathology, Institute of Cancer Sciences, College of Medical, Veterinary, and Life Sciences, University of Glasgow, Glasgow, G61 1QH, UK.ORCID http://orcid.org/0000-0002-3933-3975
Joanne EdwardsUnit of Gastrointestinal Cancer and Molecular Pathology, Institute of Cancer Sciences, College of Medical, Veterinary, and Life Sciences, University of Glasgow, Glasgow, G61 1QH, UK.ORCID http://orcid.org/0000-0002-7192-6906
University of Glasgow · GBCancer Research UK Scotland Institute · GBCancer Research UK · GBQueen Elizabeth University Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDespite increases in diagnostics and effective treatments, over 300,000 men die from prostate cancer highlighting the need for specific and differentiating biomarkers. AR phosphorylation associates with castrate-resistance, with pAR

methodsImmunohistochemistry and immunofluorescence were performed on matched hormone-naive and castrate-resistant prostate cancer samples. TempO-Seq gene profiling was analysed using DESeq2 package. LNCaP-AI cells were stimulated with DHT or EGF. WST-1 assays were performed to determine effects of Enzalutamide and BKM120 on cell viability.

resultsFollowing the development of castrate-resistance, pAR

conclusionCombined pAR

Indexed as

AgedAminopyridinesAndrogen Receptor AntagonistsBenzamidesBiomarkers, TumorCell Line, TumorCell ProliferationHumansMaleMorpholinesNitrilesPhenylthiohydantoinPhosphatidylinositol 3-KinasePhosphorylationPrognosisProstatic Neoplasms, Castration-ResistantAminopyridinesAndrogen Receptor AntagonistsAR protein, humanBenzamidesBiomarkers, TumorenzalutamideMorpholinesNitrilesNVP-BKM120PhenylthiohydantoinPhosphatidylinositol 3-KinaseReceptors, AndrogenSerine

Identifiers

PMID32358577
OpenAlexW3022810250

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.