Evidence map›Paper›PMID 29808534›Full record

ArticleJournal of cellular and molecular medicine2018

miR-21 promotes cardiac fibroblast-to-myofibroblast transformation and myocardial fibrosis by targeting Jagged1.

Xue-Liang Zhou, Hua Xu, Zhi-Bo Liu, Qi-Cai Wu, Rong-Rong Zhu, Ji-Chun Liu

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
6.8field-weighted citation impact, top 2% 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

63 citing papers in PubMed, 86 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Unifying and unique roles of non-coding RNA biomarkers in liver and heart fibrosis.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2026
    Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. RNA Therapeutics in Heart Failure.Journal of cardiovascular translational research · 2025
    Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review

3 more citing papers are in PubMed but not listed here.

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

6 authors at 2 institutions in 1 country.

Xue-Liang Zhou *Department of Cardiac Surgery, The First Affiliated Hospital, Nanchang University, Nanchang, China.
Hua Xu *Department of Cardiac Surgery, The First Affiliated Hospital, Nanchang University, Nanchang, China.
Zhi-Bo LiuDepartment of Cardiac Surgery, The First Affiliated Hospital, Nanchang University, Nanchang, China.
Qi-Cai WuDepartment of Cardiac Surgery, The First Affiliated Hospital, Nanchang University, Nanchang, China.
Rong-Rong ZhuDepartment of Obstetrics and Gynecology, Jiangxi Province hospital of integrated traditional, Nanchang, 330006, China.
Ji-Chun LiuDepartment of Cardiac Surgery, The First Affiliated Hospital, Nanchang University, Nanchang, China.ORCID http://orcid.org/0000-0003-3624-9134
Nanchang University · CNSecond Hospital of Nanchang · CN

Funding

Gan Po Talent 555 ProgramJiangxi Provincial Department of Education Science and Technology Research Project GJJ14004Jiangxi Provincial Universities Science Technology Floor Plan KJLD1401National Natural Science Foundation of China 81460065National Natural Science Foundation of China 81570262the Natural Science Foundation of Jiangxi Province 20142BAB205039the Natural Science Foundation of Jiangxi Province 20152ACB20026
6 · The paper itself

Abstract

Myocardial fibrosis after myocardial infarction (MI) is a leading cause of heart diseases. MI activates cardiac fibroblasts (CFs) and promotes CF to myofibroblast transformation (CMT). This study aimed to investigate the role of miR-21 in the regulation of CMT and myocardial fibrosis. Primary rat CFs were isolated from young SD rats and treated with TGF-β1, miR-21 sponge or Jagged1 siRNA. Cell proliferation, invasion and adhesion were detected. MI model was established in male SD rats using LAD ligation method and infected with recombinant adenovirus. The heart function and morphology was evaluated by ultrasonic and histological analysis. We found that TGF-β1 induced the up-regulation of miR-21 and down-regulation of Jagged1 in rat CFs. Luciferase assay showed that miR-21 targeted 3'-UTR of Jagged1 in rat CFs. miR-21 sponge inhibited the transformation of rat CFs into myofibroblasts, and abolished the inhibition of Jagged1 mRNA and protein expression by TGF-β1. Furthermore, these effects of miR-21 sponge on rat CFS were reversed by siRNA mediated knockdown of Jagged1. In vivo, heart dysfunction and myocardial fibrosis in MI model rats were partly improved by miR-21 sponge but were aggravated by Jagged1 knockdown. Taken together, these results suggest that miR-21 promotes cardiac fibroblast-to-myofibroblast transformation and myocardial fibrosis by targeting Jagged1. miR-21 and Jagged1 are potential therapeutic targets for myocardial fibrosis.

Indexed as

Jagged1miR-21myocardial fibrosisTGF-β1

Identifiers

PMID29808534
PMCPMC6050485
OpenAlexW2807177895

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.