Evidence map›Paper›PMID 33093529›Full record

ArticleScientific reports2020

Loss of RBMS1 as a regulatory target of miR-106b influences cell growth, gap closing and colony forming in prostate carcinoma.

Jaroslaw Thomas Dankert, Marc Wiesehöfer, Sven Wach, Elena Dilâra Czyrnik, Gunther Wennemuth

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.9field-weighted citation impact, top 31% 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

14 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
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  3. Role of the RBMS Family in Different Cancers and Research Progress.International journal of medical sciences · 2026
    Review
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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

5 authors at 2 institutions in 1 country.

Jaroslaw Thomas DankertDepartment of Anatomy, University Hospital Essen, Hufelandstr. 55, 45147, Essen, Germany.
Marc WiesehöferDepartment of Anatomy, University Hospital Essen, Hufelandstr. 55, 45147, Essen, Germany.
Sven WachInstitute of Molecular Urology, University Hospital Erlangen, Erlangen, Germany.
Elena Dilâra CzyrnikDepartment of Anatomy, University Hospital Essen, Hufelandstr. 55, 45147, Essen, Germany.
Gunther WennemuthDepartment of Anatomy, University Hospital Essen, Hufelandstr. 55, 45147, Essen, Germany. gunther.wennemuth@uk-essen.de.
Essen University Hospital · DEUniversitätsklinikum Erlangen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prostate carcinoma (PCa) is the second most commonly diagnosed cancer in males worldwide. Among hereditary genetic mutations and nutrient factors, a link between the deregulation of microRNA (miRNA) expression and the development of prostate carcinoma is assumed. MiRNAs are small non-coding RNAs which post-transcriptionally regulate gene expression and which are involved in tumour development and progression as oncogenes or tumour suppressors. Although many genes could be confirmed as targets for deregulated miRNAs, the impact of differentially expressed miRNA and their regulatory target genes on prostate tumour development and progression are not fully understood yet. We could validate RBMS1, a barely described RNA-binding protein, as a new target gene for oncogenic miR-106b, which was identified as an induced miRNA in PCa. Further analysis revealed a loss of RBMS1 expression in prostate tumours compared to corresponding normal tissue. Overexpression of RBMS1 in DU145 and LNCaP prostate cancer cells resulted in diminished cell proliferation, colony forming ability as well as in retarded gap closing. Our results demonstrate for the first time a miR-106b dependent downregulation of RBMS1 in prostate carcinoma. Additionally, we show new tumour suppressive properties of RBMS1 whose observed loss may further elucidate the development of PCa.

Indexed as

Cell ProliferationGene Expression Regulation, NeoplasticApoptosisBiomarkers, TumorCell CycleCell MovementDNA-Binding ProteinsHumansMaleMicroRNAsPrognosisProstatic NeoplasmsRNA-Binding ProteinsTumor Cells, CulturedTumor Stem Cell AssayBiomarkers, TumorDNA-Binding ProteinsMicroRNAsMIRN106 microRNA, humanRBMS1 protein, humanRNA-Binding Proteins

Identifiers

PMID33093529
PMCPMC7582885
OpenAlexW3094610463

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.