Evidence map›Paper›PMID 32089781›Full record

ArticleOxidative medicine and cellular longevity2020

Mesenchymal Stem Cells Attenuate Diabetic Lung Fibrosis via Adjusting Sirt3-Mediated Stress Responses in Rats.

Yang Chen, Fuping Zhang, Di Wang, Lan Li, Haibo Si, Chengshi Wang, Jingping Liu, Younan Chen, Jingqiu Cheng, Yanrong Lu

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

27 citing papers in PubMed, 39 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

10 authors at 1 institution in 1 country.

Yang ChenKey Laboratory of Transplant Engineering and Immunology, West China Hospital, Regenerative Medicine Research Center, Sichuan University, Chengdu 610041, China.
Fuping ZhangKey Laboratory of Transplant Engineering and Immunology, West China Hospital, Regenerative Medicine Research Center, Sichuan University, Chengdu 610041, China.
Di WangResearch Core Facility, West China Hospital, Sichuan University, Chengdu 610041, China.
Lan LiKey Laboratory of Transplant Engineering and Immunology, West China Hospital, Regenerative Medicine Research Center, Sichuan University, Chengdu 610041, China.
Haibo SiDepartment of Orthopaedics, West China Hospital, Sichuan University, Chengdu 610041, China.
Chengshi WangKey Laboratory of Transplant Engineering and Immunology, West China Hospital, Regenerative Medicine Research Center, Sichuan University, Chengdu 610041, China.
Jingping LiuKey Laboratory of Transplant Engineering and Immunology, West China Hospital, Regenerative Medicine Research Center, Sichuan University, Chengdu 610041, China.ORCID https://orcid.org/0000-0001-8364-639X
Younan ChenKey Laboratory of Transplant Engineering and Immunology, West China Hospital, Regenerative Medicine Research Center, Sichuan University, Chengdu 610041, China.
Jingqiu ChengKey Laboratory of Transplant Engineering and Immunology, West China Hospital, Regenerative Medicine Research Center, Sichuan University, Chengdu 610041, China.
Yanrong LuKey Laboratory of Transplant Engineering and Immunology, West China Hospital, Regenerative Medicine Research Center, Sichuan University, Chengdu 610041, China.ORCID https://orcid.org/0000-0002-3728-222X
Sichuan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diabetes affects a variety of organs such as the kidneys, eyes, and liver, and there is increasing evidence that the lung is also one of the target organs of diabetes and imbalance of Sirt3-mediated stress responses such as inflammation, oxidative stress, apoptosis, autophagy, and ER stress may contribute to diabetic lung fibrosis. Although previous studies have reported that mesenchymal stem cells (MSCs) have beneficial effects on various diabetic complications, the effect and mechanisms of MSCs on diabetes-induced lung injury are not clear. In this study, the STZ-induced diabetes model was constructed in rats, and the effect and potential mechanisms of bone marrow MSCs on diabetic lung fibrosis were investigated. The results revealed that fibrotic changes in the lung were successfully induced in the diabetic rats, while MSCs significantly inhibited or even reversed the changes. Specifically, MSCs upregulated the expression levels of Sirt3 and SOD2 and then activated the Nrf2/ARE signaling pathway, thereby controlling MDA, GSH content, and iNOS and NADPH oxidase subunit p22

Indexed as

AnimalsApoptosisDiabetes Mellitus, ExperimentalFibrosisLungMaleMesenchymal Stem CellsMiceRabbitsRatsRats, Sprague-DawleySirtuin 3Sirtuin 3

Identifiers

PMID32089781
PMCPMC7024095
OpenAlexW3005366991

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.