Evidence map›Paper›PMID 29574791›Full record

ArticleBritish journal of pharmacology2018

Inhibition of human prostate smooth muscle contraction by the LIM kinase inhibitors, SR7826 and LIMKi3.

Qingfeng Yu, Christian Gratzke, Yiming Wang, Annika Herlemann, Christian Maximilian Sterr, Beata Rutz, Anna Ciotkowska, Xiaolong Wang, Frank Strittmatter, Christian G Stief and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in British journal of pharmacology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
4.3field-weighted citation impact, top 6% 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

20 citing papers in PubMed, 29 citations in OpenAlex.

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  11. Cooperativity between β-agonists and c-Abl inhibitors in regulating airway smooth muscle relaxation.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
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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

11 authors at 1 institution in 1 country.

Qingfeng YuDepartment of Urology, Ludwig Maximilian University of Munich, Munich, Germany.
Christian GratzkeDepartment of Urology, Ludwig Maximilian University of Munich, Munich, Germany.
Yiming WangDepartment of Urology, Ludwig Maximilian University of Munich, Munich, Germany.
Annika HerlemannDepartment of Urology, Ludwig Maximilian University of Munich, Munich, Germany.
Christian Maximilian SterrDepartment of Urology, Ludwig Maximilian University of Munich, Munich, Germany.
Beata RutzDepartment of Urology, Ludwig Maximilian University of Munich, Munich, Germany.
Anna CiotkowskaDepartment of Urology, Ludwig Maximilian University of Munich, Munich, Germany.
Xiaolong WangDepartment of Urology, Ludwig Maximilian University of Munich, Munich, Germany.
Frank StrittmatterDepartment of Urology, Ludwig Maximilian University of Munich, Munich, Germany.
Christian G StiefDepartment of Urology, Ludwig Maximilian University of Munich, Munich, Germany.
Martin HennenbergDepartment of Urology, Ludwig Maximilian University of Munich, Munich, Germany.ORCID 0000-0003-1305-6727
Ludwig-Maximilians-Universität München · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeIn men with benign prostatic hyperplasia, increased smooth muscle tone in the prostate may lead to bladder outlet obstruction and subsequent lower urinary tract symptoms. Consequently, medical treatment aims to inhibit prostate smooth muscle contraction. However, the efficacy of the treatment options available is limited, and improved understanding of mechanisms of prostate smooth muscle contraction and identification of new targets for medical intervention are mandatory. Several studies suggest that LIM kinases (LIMKs) promote smooth muscle contraction; however, this has not yet been examined. Here, we studied effects of the LIMK inhibitors on prostate smooth muscle contraction. EXPERIMENTAL APPROACH: Human prostate tissues were obtained from radical prostatectomy. Phosphorylation of cofilin, a LIMK substrate, was examined using a phospho-specific antibody. Smooth muscle contractions were studied in organ bath experiments. KEY

resultsReal-time PCR, Western blot and immunofluorescence suggested LIMKs are expressed in smooth muscle cells of prostate tissues. Two different LIMK inhibitors, SR7826 (1 μM) and LIMKi3 (1 μM), inhibited contractions of prostate strips, which were induced by electrical field stimulation, α CONCLUSIONS AND IMPLICATIONS: Smooth muscle tone in the hyperplastic human prostate may underlie the effects of LIMKs, which promote contraction. Contraction of prostate strips can be inhibited by small molecule LIMK inhibitors.

Indexed as

Actin Depolymerizing FactorsCells, CulturedCell SurvivalElectric StimulationHumansLim KinasesMaleMuscle ContractionMuscle, SmoothProstatic NeoplasmsProtein Kinase InhibitorsPyrazolesThiazolesActin Depolymerizing FactorsLIMK1 protein, humanLIMK2 protein, humanLIMKi3Lim KinasesProtein Kinase InhibitorsPyrazolesThiazoles

Identifiers

PMID29574791
PMCPMC5978953
OpenAlexW2791940250

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.