Evidence map›Paper›PMID 37833927›Full record

ArticleInternational journal of molecular sciences2023

MiR-148a-3p within HucMSC-Derived Extracellular Vesicles Suppresses Hsp90b1 to Prevent Fibroblast Collagen Synthesis and Secretion in Silica-Induced Pulmonary Fibrosis.

Qiyue Jiang, Jing Zhao, Qiyue Jia, Hongwei Wang, Wenming Xue, Fuao Ning, Jiaxin Wang, Yan Wang, Zhonghui Zhu, Lin Tian

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. 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
2.8field-weighted citation impact, top 9% 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

10 citing papers in PubMed, 11 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.

Qiyue JiangDepartment of Occupational and Environmental Health, School of Public Health, Capital Medical University, Beijing 100069, China.
Jing ZhaoDepartment of Occupational and Environmental Health, School of Public Health, Capital Medical University, Beijing 100069, China.
Qiyue JiaDepartment of Occupational and Environmental Health, School of Public Health, Capital Medical University, Beijing 100069, China.
Hongwei WangDepartment of Occupational and Environmental Health, School of Public Health, Capital Medical University, Beijing 100069, China.
Wenming XueDepartment of Occupational and Environmental Health, School of Public Health, Capital Medical University, Beijing 100069, China.
Fuao NingDepartment of Occupational and Environmental Health, School of Public Health, Capital Medical University, Beijing 100069, China.
Jiaxin WangDepartment of Occupational and Environmental Health, School of Public Health, Capital Medical University, Beijing 100069, China.
Yan WangDepartment of Occupational and Environmental Health, School of Public Health, Capital Medical University, Beijing 100069, China.
Zhonghui ZhuDepartment of Occupational and Environmental Health, School of Public Health, Capital Medical University, Beijing 100069, China.ORCID 0000-0002-9158-0826
Lin TianDepartment of Occupational and Environmental Health, School of Public Health, Capital Medical University, Beijing 100069, China.
Capital Medical University · CN

Funding

The National Natural Science Foundation of China 81872595The National Natural Science Foundation of China 82073522
6 · The paper itself

Abstract

Silicosis is a fatal occupational respiratory disease caused by the prolonged inhalation of respirable silica. The core event of silicosis is the heightened activity of fibroblasts, which excessively synthesize extracellular matrix (ECM) proteins. Our previous studies have highlighted that human umbilical cord mesenchymal stem cell-derived extracellular vesicles (hucMSC-EVs) hold promise in mitigating silicosis and the significant role played by microRNAs (miRNAs) in this process. Delving deeper into this mechanism, we found that miR-148a-3p was the most abundant miRNA of the differential miRNAs in hucMSC-EVs, with the gene heat shock protein 90 beta family member 1 (Hsp90b1) as a potential target. Notably, miR-148a-3p's expression was downregulated during the progression of silica-induced pulmonary fibrosis both in vitro and in vivo, but was restored after hucMSC-EVs treatment (

Indexed as

Extracellular VesiclesMicroRNAsPulmonary FibrosisSilicosisCollagenFibroblastsHumansSilicon DioxideTransforming Growth Factor beta1CollagenMicroRNAsSilicon DioxideTransforming Growth Factor beta1extracellular vesiclesfibroblastsHsp90b1HucMSCsMiR-148a-3ppulmonary fibrosissilica

Identifiers

PMID37833927
PMCPMC10572270
OpenAlexW4386996841

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.