Evidence map›Paper›PMID 40688068›Full record

ArticleBioactive materials2025

Extruded nanovesicles derived from umbilical cord mesenchymal stem cells exhibit No tumorigenic potential.

Fei Wang, Lanya Li, Junyao Deng, Shushan Mo, Jiacong Ai, Yingxian Xiao, Qishan Li, Dandan Ding, Yixin Zhang, Dongfang Zhou and 1 more

Abstract read
In one paragraph

Article in Bioactive materials, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. 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

11 authors.

Fei WangThe Tenth Affiliated Hospital, Southern Medical University (Dongguan People's Hospital), Dongguan, 523059, China.
Lanya LiThe Tenth Affiliated Hospital, Southern Medical University (Dongguan People's Hospital), Dongguan, 523059, China.
Junyao DengThe Tenth Affiliated Hospital, Southern Medical University (Dongguan People's Hospital), Dongguan, 523059, China.
Shushan MoThe Tenth Affiliated Hospital, Southern Medical University (Dongguan People's Hospital), Dongguan, 523059, China.
Jiacong AiThe Tenth Affiliated Hospital, Southern Medical University (Dongguan People's Hospital), Dongguan, 523059, China.
Yingxian XiaoThe Tenth Affiliated Hospital, Southern Medical University (Dongguan People's Hospital), Dongguan, 523059, China.
Qishan LiThe Tenth Affiliated Hospital, Southern Medical University (Dongguan People's Hospital), Dongguan, 523059, China.
Dandan DingThe Tenth Affiliated Hospital, Southern Medical University (Dongguan People's Hospital), Dongguan, 523059, China.
Yixin ZhangThe Tenth Affiliated Hospital, Southern Medical University (Dongguan People's Hospital), Dongguan, 523059, China.
Dongfang ZhouSchool of Pharmaceutical Sciences, Southern Medical University, Guangzhou, 510515, China.
Zhenhua LiThe Tenth Affiliated Hospital, Southern Medical University (Dongguan People's Hospital), Dongguan, 523059, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mesenchymal stem cells (MSCs) and MSC-derived extracellular vesicles (MSC EVs) have gained significant attention in biomedical and therapeutic applications. Nevertheless, their translation in clinical practice remains limited due to the lack of scalable manufacturing techniques and the prevailing safety concerns. Cell-derived extruded nanovesicles (eNVs) with high production efficiency are regarded as promising substitutes of EVs. However, like MSC EVs, their potential for tumorigenicity has yet to be exhaustively investigated. In this work, we investigated the tumorigenicity of umbilical cord mesenchymal stem cell-derived eNVs (UMSC eNVs). A549 cancer cell-derived eNVs (A549 eNVs) with potential tumorigenicity were also prepared for comparative analysis. Our characterization findings revealed that, although UMSC eNVs and A549 eNVs exhibited similar morphologies, they differed in their molecular composition. Subsequent animal experiments demonstrated the low tumorigenicity risk of UMSC eNVs in inducing tumor pathogenesis and development. Furthermore, microRNAs (miRNAs) profiling analyses suggested that the reduced tumorigenicity of UMSC eNVs might be due to the downregulation of hsa-miR-21-5p_R+1 and hsa-miR-192-5p, and upregulation of hsa-miR-143-3p and hsa-miR-146a-5p compared to A549 eNVs. The present study provided direct experimental confirmation and underlying miRNA profiling evidence of the biosafety of UMSC eNVs in terms of tumorigenicity, which will promote the future advancement and translation of UMSC eNVs.

Indexed as

CancerExtruded nanovesiclesMesenchymal stem cellsmiRNAsTumorigenicity

Identifiers

PMID40688068
PMCPMC12271084

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.