Evidence map›Paper›PMID 25337192›Full record

ArticleInternational journal of clinical and experimental pathology2014

Intranasal sirna targeting c-kit reduces airway inflammation in experimental allergic asthma.

Wei Wu, Hui Chen, Ya-Ming Li, Sheng-Yu Wang, Xin Diao, Kai-Ge Liu

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
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  6. Article
  7. Pulmonary siRNA delivery for lung disease: Review of recent progress and challenges.Journal of controlled release : official journal of the Controlled Release Society · 2021
    Review
  8. Article
  9. Review
  10. Review
  11. Review
  12. Novel approaches to the management of noneosinophilic asthma.Therapeutic advances in respiratory disease · 2016
    Review
  13. Article
  14. Review
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 1 institution in 1 country.

Wei WuDepartment of Respiratory and Critical Care Medicine, The Affiliated Hospital of Xi'an Medical University Xi'an, China.
Hui ChenDepartment of Respiratory and Critical Care Medicine, The Affiliated Hospital of Xi'an Medical University Xi'an, China.
Ya-Ming LiDepartment of Respiratory and Critical Care Medicine, The Affiliated Hospital of Xi'an Medical University Xi'an, China.
Sheng-Yu WangDepartment of Respiratory and Critical Care Medicine, The Affiliated Hospital of Xi'an Medical University Xi'an, China.
Xin DiaoDepartment of Respiratory and Critical Care Medicine, The Affiliated Hospital of Xi'an Medical University Xi'an, China.
Kai-Ge LiuDepartment of Laboratory Medicine, The Affiliated Hospital of Xi'an Medical University Xi'an, China.
Xi'an Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Allergic asthma is characterized by airway inflammation caused by infiltration and activation of inflammatory cells that produce cytokines. Many studies have revealed that c-kit, a proto-oncogene, and its ligand, stem cell factor (SCF), play an important role in the development of asthmatic inflammation. Intranasal small interference RNA (siRNA) nanoparticles targeting specific viral gene could inhibit airway inflammation. In this study, we assessed whether silencing of c-kit with intranasal small interference RNA could reduce inflammation in allergic asthma. A mouse model of experimental asthma was treated with intranasal administration of anti-c-kit siRNA to inhibit the expression of the c-kit gene. We assessed the inflammatory response in both anti-c-kit siRNA-treated and control mice. Local administration of siRNA effectively inhibited the expression of the c-kit gene and reduced airway mucus secretion and the infiltration of eosinophils in bronchoalveolar lavage fluid. Moreover, c-kit siRNA reduced the production of SCF, interleukin-4 (IL-4), and IL-5, but had no effect on interferon-γ (IFN-γ) generation. These results show that intranasal siRNA nanoparticles targeting c-kit can decrease the inflammatory response in experimental allergic asthma.

Indexed as

RNA InterferenceAdministration, IntranasalAnimalsAsthmaBronchoalveolar Lavage FluidDisease Models, AnimalDown-RegulationGenetic TherapyInflammation MediatorsInterferon-gammaInterleukin-4Interleukin-5LungMaleMice, Inbred C57BLNanoparticlesInflammation MediatorsInterferon-gammaInterleukin-4Interleukin-5OvalbuminProto-Oncogene Proteins c-kitRNA, Small Interferingasthmac-kitgene silencinginflammationsmall interference RNA

Identifiers

PMID25337192
PMCPMC4203163
OpenAlexW2256561579

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.