Evidence map›Paper›PMID 31694982›Full record

ArticleAging2019

Long noncoding RNA DNM3OS promotes prostate stromal cells transformation via the miR-29a/29b/COL3A1 and miR-361/TGFβ1 axes.

Ruizhe Wang, Mengda Zhang, Zhenyu Ou, Wei He, Lingxiao Chen, Junjie Zhang, Yao He, Ran Xu, Shusuan Jiang, Lin Qi and 1 more

Open access · greenAbstract read
In one paragraph

Article in Aging, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

21 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
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  4. The Duality of Collagens in Metastases of Solid Tumors.International journal of molecular sciences · 2025
    Review
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  11. Review
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  16. Article
  17. Animal models of benign prostatic hyperplasia.Prostate cancer and prostatic diseases · 2021
    Review
  18. Article
  19. Article
  20. Article
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 3 institutions in 1 country.

Ruizhe WangDepartment of Urology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
Mengda ZhangDepartment of Urology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
Zhenyu OuDepartment of Urology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
Wei HeDepartment of Urology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
Lingxiao ChenDepartment of Urology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
Junjie ZhangDepartment of Urology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
Yao HeDepartment of Urology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
Ran XuDepartment of Urology, The Second Xiangya Hospital of Central South University, Changsha, Hunan 410011, China.
Shusuan JiangDepartment of Urology, Hunan Cancer Hospital and The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, Hunan 410013, China.
Lin QiDepartment of Urology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
Long WangDepartment of Urology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
Xiangya Hospital Central South University · CNCentral South University · CNHunan Cancer Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transforming growth factor-β1 (TGFβ1)-induced differentiation into and the activation of myofibroblasts have been regarded as critical events in benign prostatic hyperplasia (BPH); however, the underlying mechanisms of BPH pathogenesis remain unclear. Microarray profiling, STRING analysis, Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway annotation, and Gene Ontology (GO) enrichment analysis were performed to confirm the candidate genes and long non-coding RNA (lncRNAs) related to BPH. Collagen Type III (COL3A1) was significantly upregulated by TGFβ1 in prostate stromal cells (PrSCs) and might be involved in DNM3OS function in myofibroblasts upon TGFβ1 stimulation. Upon TGFβ1 stimulation, COL3A1 protein was decreased by DNM3OS silencing. miR-29a and miR-29b could directly bind to the DNM3OS and COL3A1 3' untranslated region (UTR)s to negatively regulate their expression, and by serving as a competing endogenous RNAs (ceRNA), DNM3OS competed with COL3A1 for miR-29a/29b binding, therefore counteracting miR-29a/29b-mediated COL3A1 suppression. The effect of DNM3OS silencing on ECM components and TGFβ1 downstream signaling was similar to that of the TGFβ1 inhibitor SB431542. miR-361 could target DNM3OS and TGFβ1; DNM3OS competed for miR-361 binding to counteract miR-361-mediated TGFβ1 suppression. In conclusion, we identified DNM3OS as a specifically-upregulated lncRNA upon TGFβ1 stimulation in PrSCs; by serving as a ceRNA for the miR-29a/29b cluster and miR-361, DNM3OS eliminated miRNA-mediated suppression of COL3A1 and TGFβ1, thereby promoting TGFβ1-induced PrSC transformation into myofibroblasts.

Indexed as

AgedCollagen Type IIIExtracellular MatrixGene Expression ProfilingHumansMaleMicroRNAsMiddle AgedMyofibroblastsOligonucleotide Array Sequence AnalysisPrimary Cell CultureProstateProstatic HyperplasiaRNA, Long NoncodingStromal CellsTransforming Growth Factor beta1COL3A1 protein, humanCollagen Type IIIMicroRNAsMIRN29a microRNA, humanMIRN361 microRNA, humanRNA, Long NoncodingTGFB1 protein, humanTransforming Growth Factor beta1benign prostatic hyperplasia (BPH)COL3A1lncRNA DNM3OSmiR-29a/29bTGF-β1

Identifiers

PMID31694982
PMCPMC6874426
OpenAlexW2985735677

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.