Evidence map›Paper›PMID 29786779›Full record

ArticleInflammation research : official journal of the European Histamine Research Society ... [et al.]2018

DNMT3A controls miR-200b in cardiac fibroblast autophagy and cardiac fibrosis.

Xu-Dong Zhao, Run-He Qin, Jing-Jing Yang, Sheng-Song Xu, Hui Tao, Xuan-Sheng Ding, Kai-Hu Shi

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In one paragraph

Article in Inflammation research : official journal of the European Histamine Research Society ... [et al.], 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.4field-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

28 citing papers in PubMed, 41 citations in OpenAlex.

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  12. Autophagy in peritoneal fibrosis.Frontiers in physiology · 2023
    Review
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  15. Article
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  17. Role of the microRNA-29 family in myocardial fibrosis.Journal of physiology and biochemistry · 2021
    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

7 authors at 4 institutions in 1 country.

Xu-Dong ZhaoDepartment of Cardiothoracic Surgery, The Second Hospital of Anhui Medical University, Fu Rong Road, Hefei, 230601, Anhui, China.
Run-He QinDepartment of Cardiothoracic Surgery, The Second Hospital of Anhui Medical University, Fu Rong Road, Hefei, 230601, Anhui, China.
Jing-Jing YangDepartment of Pharmacology, The Second Hospital of Anhui Medical University, Hefei, 230601, China.
Sheng-Song XuDepartment of Cardiothoracic Surgery, The Second Hospital of Anhui Medical University, Fu Rong Road, Hefei, 230601, Anhui, China.
Hui TaoDepartment of Cardiothoracic Surgery, The Second Hospital of Anhui Medical University, Fu Rong Road, Hefei, 230601, Anhui, China. 1272313400@qq.com.
Xuan-Sheng DingSchool of Basic Medical Sciences and Clinical Pharmacy, China Pharmaceutical University, Nanjing, 210009, China.
Kai-Hu ShiDepartment of Cardiothoracic Surgery, The Second Hospital of Anhui Medical University, Fu Rong Road, Hefei, 230601, Anhui, China. ayskh3@hotmail.com.
Anhui Medical University · CNSecond Hospital of Anhui Medical University · CNChina Pharmaceutical University · CNNanjing University of Chinese Medicine · CN

Funding

National Nature Scientific Foundation of China 81700212National Nature Scientific Foundation of China No. 81570295Natural Science Foundation of Anhui Provincial Education Department KJ2017A168
6 · The paper itself

Abstract

AIM AND

objectiveRegulation of microRNA gene expression by DNA methylation may represent a key mechanism to drive cardiac fibrosis progression. Cardiac fibroblast autophagy is the primary source of cardiac fibrosis, but the mechanisms underlying this process are incompletely understood. Here we found that DNMT3A suppression of the microRNA-200b (miR-200b) through pathway leads to cardiac fibroblast autophagy in cardiac fibrosis.

methodsTo understand the impact of DNMT3A on miR-200b at cardiac fibrosis, the rat cardiac fibrosis model was established via the abdominal aortic coarctation. Cardiac fibroblasts (CFs) were harvested from SD neonate rats and cultured. The expression of DNMT3A, miR-200b, collagen I was measured by western blotting, immunohistochemistry and qRT-PCR. Gain- or loss-of-function approaches were used to manipulate DNMT3A and miR-200b.

resultsDNMT3A level was upregulated and negatively correlated with miR-200b expression in fibrosis tissues and cardiac fibroblast. We found that autophagy was activated by miR-200b inhibitor and inactivated by miR-200b mimic in the rat cardiac fibroblast. Knockdown of DNMT3A notably increased the expression of miR-200b.

conclusionsTaken together, these findings indicate that DNMT3A regulation of miR-200b controls cardiac fibroblast autophagy during cardiac fibrosis and provide a basis for the development of therapies for cardiac fibrosis.

Indexed as

AnimalsAnimals, NewbornAutophagyCells, CulturedCollagen Type ICollagen Type I, alpha 1 ChainDNA (Cytosine-5-)-MethyltransferasesDNA Methyltransferase 3AFibroblastsFibrosisMaleMicroRNAsMicrotubule-Associated ProteinsMyocardiumRats, Sprague-DawleySirolimusAnxa3 protein, ratCollagen Type ICollagen Type I, alpha 1 ChainDNA (Cytosine-5-)-MethyltransferasesDNA Methyltransferase 3AMicroRNAsMicrotubule-Associated ProteinsMIRN200 microRNA, ratSirolimusAutophagyCardiac fibroblastCardiac fibrosisDNMT3AmiR-200b

Identifiers

PMID29786779
OpenAlexW2804652860

What OpenQuestion holds

Textmetadata
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.