Evidence map›Paper›PMID 39083104›Full record

ArticleWorld journal of urology2024

Evaluation of androgen receptor and androgen receptor splice-variant 7 in bladder cancer; a novel approach into an ancient topic.

Ege Alper Sarıkaya, Peyda Korhan, Canet Incir, Alperen H Yıldız, Dogan M Deger, Selçuk M Özer, Yesim Tuncok, Gul Ergor, Yasemin Ö Islakoğlu, Volkan Sen and 3 more

Abstract read
In one paragraph

Article in World journal of urology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–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

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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

13 authors.

Ege Alper SarıkayaDokuz Eylul University Hospital Urology Department, Edirne, Turkey. ege.sarikaya@deu.edu.tr.ORCID https://orcid.org/0000-0001-7247-1416
Peyda KorhanIzmir Biomedicine and Genome Center, Balcova, Izmir, 35340, Turkey.
Canet IncirDokuz Eylul University Hospital Medical Pharmacology Department, İzmir, Turkey.
Alperen H YıldızBolu Abant Izzet Baysal Üniversitesi Faculty of Medicine University Hospital Urology Department, Bolu, Turkey.
Dogan M DegerEdirne Sultan 1. Murat State Hospital, Edirne, Turkey.
Selçuk M ÖzerDokuz Eylul University Hospital Urology Department, Edirne, Turkey.
Yesim TuncokDokuz Eylul University Hospital Medical Pharmacology Department, İzmir, Turkey.
Gul ErgorDokuz Eylul University Hospital Public Health Department, Izmir, Turkey.
Yasemin Ö IslakoğluIzmir Biomedicine and Genome Center, Balcova, Izmir, 35340, Turkey.
Volkan SenDokuz Eylul University Hospital Urology Department, Edirne, Turkey.
Ozan BozkurtDokuz Eylul University Hospital Urology Department, Edirne, Turkey.
Neşe AtabeyIzmir Biomedicine and Genome Center, Balcova, Izmir, 35340, Turkey.
Adil A EsenDokuz Eylul University Hospital Urology Department, Edirne, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe contribution of androgen receptors (AR) on bladder cancer has been demonstrated in pre-clinical studies, however in clinical studies, only the canonical AR (AR-FL) protein was measured by immunohistochemistry and conflicting results were obtained. To get better insight into the alterations of AR signalling, we used western blotting (WB) method and simultaneously measured both mRNA and protein levels of AR-FL and AR-V7.

methods23 naive non-muscle invasive bladder cancer patients and 12 healthy individuals were included. AR-FL protein, AR-FL mRNA, AR-V7 protein and AR-V7 mRNA levels were quantitatively measured by WB and qRT-PCR.

resultsWhile AR-FL protein and AR-V7 mRNA were significantly higher in bladder cancer, AR-FL mRNA and AR-V7 protein were lower. AR-V7 mRNA level was higher in patients with tumour size over 3 cm and AR-FL protein was higher in single tumours (p < 0,005). The small sampling size and the inclusion of only male participants were the main limitations.

conclusionsThe increase of AR-FL protein in bladder cancer supports the contribution of the AR pathway in bladder cancer. The presence of high AR-FL protein despite low mRNA levels may be due to a disruption in post-transcriptional regulatory mechanisms. AR-V7 was demonstrated for the first time in bladder tissue and found significantly different in bladder cancer tissues. Our study reached new and valuable findings and will shed light on the studies that aim to clarify the role of the AR pathway in bladder cancer.

Indexed as

Receptors, AndrogenUrinary Bladder NeoplasmsAgedAged, 80 and overFemaleHumansMaleMiddle AgedProtein IsoformsRNA, MessengerAR protein, humanProtein IsoformsReceptors, AndrogenRNA, MessengerAndrogen receptorAndrogen receptor splice variant 7Bladder cancerWestern blotting

Identifiers

PMID39083104
PMCPMC11291539

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.