Evidence map›Paper›PMID 27061862›Full record

ArticleJournal of cellular and molecular medicine2016

miR-19b controls cardiac fibroblast proliferation and migration.

Chongjun Zhong, Kun Wang, Ying Liu, Dongchao Lv, Bo Zheng, Qiulian Zhou, Qi Sun, Ping Chen, Shengguang Ding, Yiming Xu and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2016. 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
2.9field-weighted citation impact, top 10% 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, 40 citations in OpenAlex.

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  16. The diagnostic value of circulating microRNAs in heart failure.Experimental and therapeutic medicine · 2019
    Review
  17. Article
  18. MicroRNA-183-5p Inhibits Aggressiveness of Cervical Cancer Cells by Targeting Integrin Subunit Beta 1 (ITGB1).Medical science monitor : international medical journal of experimental and clinical research · 2018
    Article
  19. Article
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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 at 8 institutions in 1 country.

Chongjun ZhongDepartment of Thoracic and Cardiovascular Surgery, The Second Affiliated Hospital of NanTong University, Nantong, China.
Kun WangDepartment of Thoracic and Cardiovascular Surgery, The Second Affiliated Hospital of NanTong University, Nantong, China.
Ying LiuDepartment of Cardiology, Shanghai Putuo District Central Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Dongchao LvSchool of Life Science, Shanghai University, Shanghai, China.
Bo ZhengShanghai Institute of Biological Products Co., Ltd, Shanghai, China.
Qiulian ZhouSchool of Life Science, Shanghai University, Shanghai, China.
Qi SunSchool of Life Science, Shanghai University, Shanghai, China.
Ping ChenSchool of Life Science, Shanghai University, Shanghai, China.
Shengguang DingDepartment of Thoracic and Cardiovascular Surgery, The Second Affiliated Hospital of NanTong University, Nantong, China.
Yiming XuDepartment of Thoracic and Cardiovascular Surgery, The Second Affiliated Hospital of NanTong University, Nantong, China.
Haitao HuangDepartment of Thoracic and Cardiovascular Surgery, The Second Affiliated Hospital of NanTong University, Nantong, China.
Second Affiliated Hospital of Nantong UniversityShanghai University · CNAffiliated Hospital of Nantong University · CNCentral Hospital of Putuo District · CNNantong University · CNShanghai FRP Research Institute (China) · CNShanghaiTech University · CNShanghai University of Engineering Science · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cardiac fibrosis is a fundamental constituent of a variety of cardiac dysfunction, making it a leading cause of death worldwide. However, no effective treatment for cardiac fibrosis is available. Therefore, novel therapeutics for cardiac fibrosis are highly needed. Recently, miR-19b has been found to be able to protect hydrogen peroxide (H2 O2 )-induced apoptosis and improve cell survival in H9C2 cardiomyocytes, while down-regulation of miR-19b had opposite effects, indicating that increasing miR-19b may be a new therapeutic strategy for attenuating cellular apoptosis during myocardial ischaemia-reperfusion injury. However, considering the fact that microRNAs might exert a cell-specific role, it is highly interesting to determine the role of miR-19b in cardiac fibroblasts. Here, we found that miR-19b was able to promote cardiac fibroblast proliferation and migration. However, miR-19b mimics and inhibitors did not modulate the expression level of collagen I. Pten was identified as a target gene of miR-19b, which was responsible for the effect of miR-19b in controlling cardiac fibroblast proliferation and migration. Our data suggest that the role of miR-19b is cell specific, and systemic miR-19b targeting in cardiac remodelling might be problematic. Therefore, it is highly needed and also urgent to investigate the role of miR-19b in cardiac remodelling in vivo.

Indexed as

Cell MovementAnimalsAnimals, NewbornCell ProliferationFibroblastsMicroRNAsMyocardiumPTEN PhosphohydrolaseRats, Sprague-DawleyMicroRNAsMIRN19 microRNA, ratPTEN Phosphohydrolasecardiac fibrosismiR-19bPten

Identifiers

PMID27061862
PMCPMC4882982
OpenAlexW2319791936

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.