Evidence map›Paper›PMID 35454085›Full record

ReviewBiomolecules2022

MicroRNAs in Pulmonary Hypertension, from Pathogenesis to Diagnosis and Treatment.

Junhua Xu, John Linneman, Yanfeng Zhong, Haoyang Yin, Qinyi Xia, Kang Kang, Deming Gou

Open access · goldAbstract readReview
In one paragraph

Review in Biomolecules, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

17 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
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  4. Article
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  6. Observational
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  8. Review
  9. The pharmaco-epigenetics of hypertension: a focus on microRNA.Molecular and cellular biochemistry · 2024
    Review
  10. microRNA-based electrochemical biosensor for early detection of pulmonary arterial hypertension.Hypertension research : official journal of the Japanese Society of Hypertension · 2024
    Article
  11. Review
  12. Article
  13. Review
  14. 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

7 authors at 2 institutions in 2 countries.

Junhua XuShenzhen Key Laboratory of Microbial Genetic Engineering, Vascular Disease Research Center, Department of Biotechnology, College of Life Sciences and Oceanography, Shenzhen University, Shenzhen 518060, China.
John LinnemanSchool of Medicine, Washington University, 12275, St. Louis, MO 63110, USA.
Yanfeng ZhongShenzhen Key Laboratory of Microbial Genetic Engineering, Vascular Disease Research Center, Department of Biotechnology, College of Life Sciences and Oceanography, Shenzhen University, Shenzhen 518060, China.
Haoyang YinShenzhen Key Laboratory of Microbial Genetic Engineering, Vascular Disease Research Center, Department of Biotechnology, College of Life Sciences and Oceanography, Shenzhen University, Shenzhen 518060, China.
Qinyi XiaShenzhen Key Laboratory of Microbial Genetic Engineering, Vascular Disease Research Center, Department of Biotechnology, College of Life Sciences and Oceanography, Shenzhen University, Shenzhen 518060, China.
Kang KangShenzhen Key Laboratory of Microbial Genetic Engineering, Vascular Disease Research Center, Department of Biotechnology, College of Life Sciences and Oceanography, Shenzhen University, Shenzhen 518060, China.
Deming GouShenzhen Key Laboratory of Microbial Genetic Engineering, Vascular Disease Research Center, Department of Biotechnology, College of Life Sciences and Oceanography, Shenzhen University, Shenzhen 518060, China.
Shenzhen University · CNWashington University in St. Louis · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pulmonary hypertension (PH) is a fatal and untreatable disease, ultimately leading to right heart failure and eventually death. microRNAs are small, non-coding endogenous RNA molecules that can regulate gene expression and influence various biological processes. Changes in microRNA expression levels contribute to various cardiovascular disorders, and microRNAs have been shown to play a critical role in PH pathogenesis. In recent years, numerous studies have explored the role of microRNAs in PH, focusing on the expression profiles of microRNAs and their signaling pathways in pulmonary artery smooth muscle cells (PASMCs) or pulmonary artery endothelial cells (PAECs), PH models, and PH patients. Moreover, certain microRNAs, such as miR-150 and miR-26a, have been identified as good candidates of diagnosis biomarkers for PH. However, there are still several challenges for microRNAs as biomarkers, including difficulty in normalization, specificity in PH, and a lack of longitudinal and big sample-sized studies. Furthermore, microRNA target drugs are potential therapeutic agents for PH treatment, which have been demonstrated in PH models and in humans. Nonetheless, synthetic microRNA mimics or antagonists are susceptible to several common defects, such as low drug efficacy, inefficient drug delivery, potential toxicity and especially, off-target effects. Therefore, finding clinically safe and effective microRNA drugs remains a great challenge, and further breakthrough is urgently needed.

Indexed as

Hypertension, PulmonaryMicroRNAsBiomarkersCell ProliferationCells, CulturedEndothelial CellsHumansPulmonary ArteryBiomarkersMicroRNAsdiagnostic biomarkermicroRNAsmicroRNA target drugsoff-target effectspulmonary hypertension

Identifiers

PMID35454085
PMCPMC9031307
OpenAlexW4220720621

What Socratic 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 Socratic graph.