Evidence map›Paper›PMID 34638915›Full record

ArticleInternational journal of molecular sciences2021

miR-29a-3p/THBS2 Axis Regulates PAH-Induced Cardiac Fibrosis.

Chih-Hsin Hsu, I-Fan Liu, Hsuan-Fu Kuo, Chia-Yang Li, Wei-Shiung Lian, Chia-Yuan Chang, Yung-Hsiang Chen, Wei-Lun Liu, Chi-Yu Lu, Yu-Ru Liu and 5 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
7.0field-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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 62 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Neuregulin-1β Mitigates Doxorubicin-Induced Cardiotoxicity viaInternational journal of molecular sciences · 2026
    Article
  4. Article
  5. Review
  6. The Role of Thrombospondin-2 in Myocardial Fibrosis.Drug design, development and therapy · 2026
    Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Gene- and cell-based therapy in cardiovascular diseases.Journal of cardiovascular pharmacology · 2025
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Expression Profiles and Bioinformatic Analysis of Circular RNAs in Db/Db Mice with Cardiac Fibrosis.Diabetes, metabolic syndrome and obesity : targets and therapy · 2024
    Article
  20. Article
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

15 authors at 7 institutions in 1 country.

Chih-Hsin HsuDepartment of Internal Medicine, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan 704, Taiwan.
I-Fan LiuInstitute of Clinical Medicine, National Yang Ming Chiao Tung University, Taipei 112, Taiwan.
Hsuan-Fu KuoGraduate Institute of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan.
Chia-Yang LiGraduate Institute of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan.ORCID 0000-0001-5689-9850
Wei-Shiung LianCore Laboratory for Phenomics and Diagnostic, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung 833, Taiwan.
Chia-Yuan ChangDepartment of Mechanical Engineering, National Cheng Kung University, Tainan 701, Taiwan.ORCID 0000-0003-0587-0868
Yung-Hsiang ChenGraduate Institute of Integrated Medicine, College of Chinese Medicine, China Medical University, Taichung 404, Taiwan.ORCID 0000-0002-8756-5113
Wei-Lun LiuSchool of Medicine, College of Medicine, Fu Jen Catholic University, New Taipei City 242, Taiwan.ORCID 0000-0001-8593-8492
Chi-Yu LuDepartment of Biochemistry, College of Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan.
Yu-Ru LiuDepartment of Respiratory Therapy, College of Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan.ORCID 0000-0002-4082-8588
Tzu-Chieh LinGraduate Institute of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan.
Tsung-Ying LeeDepartment of Respiratory Therapy, College of Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan.
Chi-Yuan HuangDepartment of Respiratory Therapy, College of Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan.ORCID 0000-0002-8462-0869
Chong-Chao HsiehGraduate Institute of Clinical Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan.
Po-Len LiuSchool of Medicine, College of Medicine, Fu Jen Catholic University, New Taipei City 242, Taiwan.ORCID 0000-0003-2896-1666
Kaohsiung Medical University · TWFu Jen Catholic University · TWAsia University · TWKaohsiung Chang Gung Memorial Hospital · TWNational Cheng Kung University · TWNational Cheng Kung University Hospital · TWNational Yang Ming Chiao Tung University · TW

Funding

Kaohsiung Medical University Chung-Ho Memorial Hospital KMUH107-7M18 and KMUH108-8M27Kaohsiung Municipal Ta-Tung Hospital Research Foundation KMTTH-108-019 and KMTTH-105-015Ministry of Science and Technology, Taiwan MOST109-2314-B-006-094-MY3, MOST104-2314-B-037-081-MY2, and MOST107-2314-B-037-074
6 · The paper itself

Abstract

Pulmonary artery hypertension (PAH) pathology involves extracellular matrix (ECM) remodeling in cardiac tissues, thus promoting cardiac fibrosis progression. miR-29a-3p reportedly inhibits lung progression and liver fibrosis by regulating ECM protein expression; however, its role in PAH-induced fibrosis remains unclear. In this study, we aimed to investigate the role of miR-29a-3p in cardiac fibrosis progression in PAH and its influence on ECM protein thrombospondin-2 (THBS2) expression. The diagnostic and prognostic values of miR-29a-3p and THBS2 in PAH were evaluated. The expressions and effects of miR-29a-3p and THBS2 were assessed in cell culture, monocrotaline-induced PAH mouse model, and patients with PAH. The levels of circulating miR-29a-3p and THBS2 in patients and mice with PAH decreased and increased, respectively. miR-29a-3p directly targets THBS2 and regulates THBS2 expression via a direct anti-fibrotic effect on PAH-induced cardiac fibrosis. The circulating levels of miR-29a-3p and THBS2 were correlated with PAH diagnostic parameters, suggesting their independent prognostic value. miR-29a-3p targeted THBS2 expression via a direct anti-fibrotic effect on PAH-induced cardiac fibrosis, indicating miR-29a-3p acts as a messenger with promising therapeutic effects.

Indexed as

Gene Expression RegulationAdultAgedAged, 80 and overAnimalsDisease Models, AnimalFemaleFibrosisHumansMaleMiceMicroRNAsMicroscopy, Electron, TransmissionMiddle AgedMyocardiumProteomicsMicroRNAsMIRN29a microRNA, humanThrombospondin 2ThrombospondinscardiomyocytesfibrosismiR-29a-3ppulmonary arterial hypertensionTHBS2

Identifiers

PMID34638915
PMCPMC8509017
OpenAlexW3203372141

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Registered trials

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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.