Evidence map›Paper›PMID 23853098›Full record

ArticleThe Journal of biological chemistry2013

MicroRNA-124 suppresses the transactivation of nuclear factor of activated T cells by targeting multiple genes and inhibits the proliferation of pulmonary artery smooth muscle cells.

Kang Kang, Xiao Peng, Xiaoying Zhang, Yuna Wang, Lishu Zhang, Li Gao, Tingting Weng, Honghao Zhang, Ramaswamy Ramchandran, J Usha Raj and 2 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

78 citing papers in PubMed, 123 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
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  6. PTBP1 as a potential regulator of disease.Molecular and cellular biochemistry · 2024
    Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. JBMR plus · 2023
    Article
  13. Review
  14. Review
  15. Research progress on the mechanism of phenotypic transformation of pulmonary artery smooth muscle cells induced by hypoxia.Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2022
    Review
  16. Increased miR-124-3p alleviates type 2 inflammatory response in allergic rhinitis via IL-4Rα.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2022
    Article
  17. Article
  18. Article
  19. Review
  20. Article

18 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

12 authors at 3 institutions in 2 countries.

Kang KangFrom the College of Life Sciences, Shenzhen Key Laboratory of Microbial Genetic Engineering, Shenzhen University, Shenzhen, Guangdong 518060, China.
Xiao PengFrom the College of Life Sciences, Shenzhen Key Laboratory of Microbial Genetic Engineering, Shenzhen University, Shenzhen, Guangdong 518060, China.
Xiaoying ZhangFrom the College of Life Sciences, Shenzhen Key Laboratory of Microbial Genetic Engineering, Shenzhen University, Shenzhen, Guangdong 518060, China.
Yuna WangFrom the College of Life Sciences, Shenzhen Key Laboratory of Microbial Genetic Engineering, Shenzhen University, Shenzhen, Guangdong 518060, China.
Lishu Zhangthe Department of Physiological Sciences, Oklahoma State University, Stillwater, Oklahoma 74078, and.
Li Gaothe Department of Physiological Sciences, Oklahoma State University, Stillwater, Oklahoma 74078, and.
Tingting Wengthe Department of Physiological Sciences, Oklahoma State University, Stillwater, Oklahoma 74078, and.
Honghao Zhangthe Department of Physiological Sciences, Oklahoma State University, Stillwater, Oklahoma 74078, and.
Ramaswamy Ramchandranthe Department of Pediatrics, University of Illinois, Chicago, Illinois 60612.
J Usha Rajthe Department of Pediatrics, University of Illinois, Chicago, Illinois 60612.
Deming GouFrom the College of Life Sciences, Shenzhen Key Laboratory of Microbial Genetic Engineering, Shenzhen University, Shenzhen, Guangdong 518060, China,; the Department of Physiological Sciences, Oklahoma State University, Stillwater, Oklahoma 74078, and; the Department of Pediatrics, University of Illinois, Chicago, Illinois 60612. Electronic address: dmgou@szu.edu.cn.
Lin Liuthe Department of Physiological Sciences, Oklahoma State University, Stillwater, Oklahoma 74078, and. Electronic address: lin.liu@okstate.edu.
Oklahoma State University · USShenzhen University · CNUniversity of Illinois Chicago · US

Funding

Functional Heterogeneity of Pulmonary Arteries and VeinsR01HL075187 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI RAJ, J. USHA · 2003 to 2011
$3.8M
MOLECULAR MECHANISMS OF LUNG SURFACTANT SECRETIONR01HL052146 · NHLBI · OKLAHOMA STATE UNIVERSITY STILLWATER · PI LIU, LIN · 2000 to 2007
$2.3M
Mechanisms of Alveolar Fluid TransportR01HL083188 · NHLBI · OKLAHOMA STATE UNIVERSITY STILLWATER · PI LIU, LIN · 2006 to 2009
$1.4M
Mechanisms of Alveolar Epithelial Cell DifferentiationR01HL071628 · NHLBI · OKLAHOMA STATE UNIVERSITY STILLWATER · PI LIU, LIN · 2003 to 2006
$1.2M
NHLBI NIH HHS R01 HL052146NHLBI NIH HHS R01 HL071628NHLBI NIH HHS R01 HL075187NHLBI NIH HHS R01 HL083188
6 · The paper itself

Abstract

Abnormal proliferation and phenotypic modulation of pulmonary artery smooth muscle cells (PASMC) contributes to the pathogenesis of numerous cardiovascular disorders, including pulmonary arterial hypertension (PAH). The nuclear factor of activated T cells (NFAT) signaling pathway is linked to PASMC proliferation and PAH. MicroRNAs (miRNAs) are small non-coding RNAs that function in diverse biological processes. To systemically identify the specific miRNAs that regulate the NFAT pathway, a human primary miRNA library was applied for cell-based high throughput screening with the NFAT luciferase reporter system. Eight miRNAs were found to modulate NFAT activity efficiently. Of them, miR-124 robustly inhibited NFAT reporter activity and decreased both the dephosphorylation and the nuclear translocation of NFAT. miR-124 also inhibited NFAT-dependent transcription of IL-2 in Jurkat T cells. miR-124 exerted its effects by targeting multiple genes, including a known component of the NFAT pathway, NFATc1, and two new regulators of NFAT signaling, CAMTA1 (calmodulin-binding transcription activator 1) and PTBP1 (polypyrimidine tract-binding protein 1). Physiologically, miR-124 was down-regulated by hypoxia in human PASMC, consistent with the activation of NFAT during this process. Down-regulation of miR-124 was also observed in 3-week hypoxia-treated mouse lungs. Furthermore, the overexpression of miR-124 not only inhibited human PASMC proliferation but also maintained its differentiated phenotype by repressing the NFAT pathway. Taken together, our data provide the first evidence that miR-124 acts as an inhibitor of the NFAT pathway. Down-regulation of miR-124 in hypoxia-treated PASMC and its antiproliferative and prodifferentiation effects imply a potential value for miR-124 in the treatment of PAH.

Indexed as

Cell ProliferationTranscriptional ActivationAnimalsCell HypoxiaDown-RegulationHumansHypertension, PulmonaryJurkat CellsMiceMicroRNAsMuscle, Smooth, VascularMyocytes, Smooth MuscleNFATC Transcription FactorsPulmonary ArterySignal TransductionMicroRNAsMIRN124 microRNA, humanMirn124 microRNA, mouseNFATC Transcription FactorsGene RegulationHigh Throughput Screening (HTS)ImmunosuppressorMicroRNANFAT Transcription FactorPulmonary Hypertension

Identifiers

PMID23853098
PMCPMC3757204
OpenAlexW2034942408

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.