Evidence map›Paper›PMID 40001250›Full record

ArticleStem cell research & therapy2025

Melatonin-pretreated mesenchymal stem cell-derived exosomes alleviate cavernous fibrosis in a rat model of nerve injury-induced erectile dysfunction via miR-145-5p/TGF-β/Smad axis.

Xiaolin Zhang, Mengbo Yang, Xinda Chen, Ming Zhang, Yiliang Peng, Mujun Lu

Abstract read
In one paragraph

Article in Stem cell research & therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–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

10 citing papers in PubMed.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Melatonin and angiogenesis potential in stem cells.Stem cell research & therapy · 2025
    Review
  10. 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

6 authors.

Xiaolin Zhang *Department of Urology and Andrology, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, NO. 145 Middle Shandong Road, Shanghai, 200001, China.
Mengbo Yang *Department of Urology and Andrology, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, NO. 145 Middle Shandong Road, Shanghai, 200001, China.
Xinda ChenDepartment of Urology and Andrology, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, NO. 145 Middle Shandong Road, Shanghai, 200001, China.
Ming ZhangDepartment of Urology and Andrology, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, NO. 145 Middle Shandong Road, Shanghai, 200001, China.
Yiliang PengDepartment of Urology and Andrology, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, NO. 145 Middle Shandong Road, Shanghai, 200001, China.
Mujun LuDepartment of Urology and Andrology, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, NO. 145 Middle Shandong Road, Shanghai, 200001, China. lumujun@sjtu.edu.cn.ORCID http://orcid.org/0000-0002-5946-2061

Funding

Key Technologies Research and Development Program SQ2024YFA1100180National Natural Science Foundation of China 82171611National Natural Science Foundation of China 82371631National Natural Science Foundation of China 82401887
6 · The paper itself

Abstract

backgroundCavernous nerve injury-induced erectile dysfunction (CNI-ED) is a common complication after radical prostatectomy. Conventional treatment approaches have had little success in treating the severe cavernous fibrosis which is a consequence of CNI-ED.

methodsPre-treatment of adipose-derived stem cells with melatonin allows for the extraction of active exosomes (MT-hASC-EVs) from the conditioned medium. The therapeutic effects of MT-hASC-EVs were assessed in a rat model of CNI-ED, and the anti-fibrotic properties were evaluated. MicroRNA sequencing was used to identify specific microRNAs highly expressed in MT-hASC-EVs, and differential microRNAs were screened for regulatory pathways through target gene enrichment analysis. Finally, the conclusions from bioinformatics analysis were validated through in vitro experiments.

resultsIntracavernous injection of MT-hASC-EVs significantly restored erectile function and reduced the extent of corpus cavernosum fibrosis in the CNI-ED rat model. MT-hASC-EVs promoted the proliferation and anti-apoptotic effects of corpus cavernosum smooth muscle cells (CCSMCs) in vitro. Mechanistically, MT-hASC-EVs inhibit fibrosis by delivering miR-145-5p, which targets TGF-β2/Smad3 axis.

conclusionsMT-hASCs-EVs can inhibit cavernous fibrosis and improve erectile function in a rat model of CNI-ED by targeting the miR-145-5p/TGF-β/Smad axis.

Indexed as

Erectile DysfunctionExosomesMelatoninMesenchymal Stem CellsMicroRNAsAnimalsDisease Models, AnimalFibrosisMalePenisRatsRats, Sprague-DawleySignal TransductionSmad ProteinsTransforming Growth Factor betaMelatoninMicroRNAsMIRN145 microRNA, ratSmad ProteinsTransforming Growth Factor betaCavernous fibrosisCNI-EDExosomeMelatoninMesenchymal stem cell

Identifiers

PMID40001250
PMCPMC11863846

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Registered trials

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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.