Evidence map›Paper›PMID 37645613›Full record

ArticleAmerican journal of clinical and experimental urology2023

EZH2 and matrix co-regulate phenotype and KCNB2 expression in bladder smooth muscle cells.

Priyank Yadav, Tabina Ahmed, Suejean Park, Martin Sidler, Annette Schröder, Karen J Aitken, Darius Bägli

Open access · greenAbstract read
In one paragraph

Article in American journal of clinical and experimental urology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.9field-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

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

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 1 institution in 1 country.

Priyank YadavThe Hospital for Sick Children Toronto, Ontario, Canada.
Tabina AhmedThe Hospital for Sick Children Toronto, Ontario, Canada.
Suejean ParkThe Hospital for Sick Children Toronto, Ontario, Canada.
Martin SidlerPaediatric and Neonatal Surgery, Klinikum Stuttgart Stuttgart, Baden-Württemberg, Germany.
Annette SchröderDepartment of Urology and Pediatric Urology of The University Medical Center Mainz Mainz, Rheinland-Pfalz, Germany.
Karen J AitkenThe Hospital for Sick Children Toronto, Ontario, Canada.
Darius BägliThe Hospital for Sick Children Toronto, Ontario, Canada.
Hospital for Sick Children · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPartial bladder outlet obstruction (PBO) is a widespread cause of urinary dysfunction and patient discomfort, resulting in immense health care costs. Previously, we found that obstruction is associated with altered regulation of epigenetic machinery and altered function. Here we examined if PBO and chronic bladder obstructive disease (COBD) affect epigenetic marks in a proof of principle gene and explored mechanisms of its epigenetic regulation using

methodsArchival obstruction tissues from COBD had been created in 200-250 g female Sprague-Dawley rats by surgical ligation of the urethra for 6 weeks, followed by removal of the suture and following animals for 6 more weeks. Obstruction (PBO) is the 6-week ligation only. Sham ligations comprise passing the suture behind the urethra. Histone3 lysine27 trimethylation (H3K27me3) was studied by immunostaining and Chromatin immunoprecipitation (ChIP)/PCR. The interaction of matrix with KCNB2 regulation was studied in human bladder SMC plated on damaged matrix and native collagen and treated with vehicle or UNC1999. Cells were analyzed by immunostaining for cell phenotype, and western blotting for KCNB2, H3K27me3 and EZH2. Effects of conditioned media from these cells were also examined on cell phenotype. siRNA against KCNB2 was examined for effects on cell phenotype and gene expression by RT-qPCR.

resultsH3K27me3 increased by immunofluorescence during PBO, and by ChIP/PCR during COBD in the CpG Island (CGI) as well as 350 bp upstream. Obstruction vs. sham also showed an increase in H3K27me3 deposition. In SMC

conclusionsRegulation of KCNB2 at the promoter demonstrated dynamic changes in H3K27me3 during COBD and obstruction.

Indexed as

Bladder obstructionepigeneticsH3K27me3matrix biologypotassium channelssmooth muscle

Identifiers

PMID37645613
PMCPMC10461034
OpenAlexW4386272257

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.