Evidence map›Paper›PMID 33482923›Full record

ArticleStem cell research & therapy2021

The delivery of hsa-miR-11401 by extracellular vesicles can relieve doxorubicin-induced mesenchymal stem cell apoptosis.

Huifang Li, Haoyan Huang, Xiaoniao Chen, Shang Chen, Lu Yu, Chen Wang, Yue Liu, Kaiyue Zhang, Lingling Wu, Zhong-Chao Han and 3 more

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

9 citing papers in PubMed, 21 citations in OpenAlex.

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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

13 authors at 3 institutions in 1 country.

Huifang LiNankai University School of Medicine, Tianjin, China.
Haoyan HuangNankai University School of Medicine, Tianjin, China.
Xiaoniao ChenBeijing Tongren Eye Center, Beijing Tongren Hospital, Capital Medical University, Beijing, 100730, China.
Shang ChenNankai University School of Medicine, Tianjin, China.
Lu YuNankai University School of Medicine, Tianjin, China.
Chen WangNankai University School of Medicine, Tianjin, China.
Yue LiuNankai University School of Medicine, Tianjin, China.
Kaiyue ZhangNankai University School of Medicine, Tianjin, China.
Lingling WuState Key Laboratory of Kidney Diseases, Chinese PLA General Hospital, Beijing, 100853, China.
Zhong-Chao HanJiangxi Engineering Research Center for Stem Cell, Shangrao, Jiangxi, China.
Na LiuNankai University School of Medicine, Tianjin, China. liuna@nankai.edu.cn.ORCID 0000-0003-3832-5591
Jie WuState Key Laboratory of Kidney Diseases, Chinese PLA General Hospital, Beijing, 100853, China. wujie301@126.com.
Zongjin LiNankai University School of Medicine, Tianjin, China. zongjinli@nankai.edu.cn.
Nankai University · CNChinese PLA General Hospital · CNBeijing Tongren Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChemotherapy is an effective anti-tumor treatment. Mesenchymal stem cells (MSCs), exerting therapy effect on injured tissues during chemotherapy, may be damaged in the process. The possibility of self-healing through long-range paracrine and the mechanisms are unclear.

methodsDoxorubicin, a commonly used chemotherapy drug, was to treat human umbilical cord-derived mesenchymal stem cells (hUC-MSCs) for 6 h as an in vitro cell model of chemotherapy-induced damage. Then we use extracellular vesicles derived from placental mesenchymal stem cells (hP-MSCs) to investigate the therapeutic potential of MSCs-EVs for chemotherapy injury. The mechanism was explored using microRNA sequencing.

resultsMSC-derived extracellular vesicles significantly alleviated the chemotherapy-induced apoptosis. Using microRNA sequencing, we identified hsa-miR-11401, which was downregulated in the Dox group but upregulated in the EV group. The upregulation of hsa-miR-11401 reduced the expression of SCOTIN, thereby inhibiting p53-dependent cell apoptosis.

conclusionsHsa-miR-11401 expressed by MSCs can be transported to chemotherapy-damaged cells by EVs, reducing the high expression of SCOTIN in damaged cells, thereby inhibiting SCOTIN-mediated apoptosis.

Indexed as

Extracellular VesiclesMesenchymal Stem CellsMicroRNAsApoptosisDoxorubicinFemaleHumansPlacentaPregnancyDoxorubicinMicroRNAsDoxorubicinExtracellular vesicles (EVs)Hsa-miR-11401Mesenchymal stem cells (MSCs)

Identifiers

PMID33482923
PMCPMC7821514
OpenAlexW3122075731

What OpenQuestion holds

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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.