Evidence map›Paper›PMID 28662100›Full record

ArticlePloS one2017

miR-146a, miR-146b, and miR-155 increase expression of IL-6 and IL-8 and support HSP10 in an In vitro sepsis model.

Dagmar Pfeiffer, Eva Roßmanith, Ingrid Lang, Dieter Falkenhagen

Open access · goldAbstract readComparative Study
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

55 citing papers in PubMed, 76 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Observational
  8. MicroRNA as Sepsis Biomarkers: A Comprehensive Review.International journal of molecular sciences · 2024
    Review
  9. Article
  10. Review
  11. MicroRNA Profiles in Critically Ill Patients.Current medicinal chemistry · 2024
    Review
  12. Review
  13. Urinary microRNAs in sepsis function as a novel prognostic marker.Experimental and therapeutic medicine · 2023
    Article
  14. Effect of thymoquinone on sepsis-induced cardiac damageThe Journal of international medical research · 2022
    Article
  15. Role of miRNA dysregulation in sepsis.Molecular medicine (Cambridge, Mass.) · 2022
    Review
  16. Observational
  17. Review
  18. Role of microRNAs in COVID-19 with implications for therapeutics.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2021
    Review
  19. 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

4 authors at 2 institutions in 1 country.

Dagmar PfeifferInstitute of Cell Biology, Histology and Embryology, Medical University Graz, Graz, Austria.ORCID http://orcid.org/0000-0002-7319-5377
Eva RoßmanithCenter of Biomedical Technology, Danube University Krems, Krems, Austria.
Ingrid LangInstitute of Cell Biology, Histology and Embryology, Medical University Graz, Graz, Austria.
Dieter FalkenhagenCenter of Biomedical Technology, Danube University Krems, Krems, Austria.
Universität für Weiterbildung Krems · ATMedical University of Graz · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

microRNAs (miRNAs) play an essential role in inflammation processes including sepsis. This study aimed to identify miRNAs as candidates for therapies that are involved in the innate immune response and to assess their potential functions in the activation of the endothelium. We stimulated THP-1 monocytes with 10 ng/ml LPS for 4 h and used the supernatant for the stimulation of human umbilical vein endothelial cells (HUVEC) or human pulmonary microvascular endothelial cells (HPMEC) for 16 h. miRNA array analysis (of 1,891 miRNAs) identified a 1.5-fold upregulation of miR-146a, miR-146b, and miR-155 in stimulated endothelial cells. HUVEC were transfected with miRNA inhibitors for miR-146a, miR-146b, and miR-155 to investigate the function of these miRNAs in endothelial inflammatory pathways. Inhibition of miR-146a resulted in a diminished release of interleukin (IL)-6 and IL-8 by respective 68% and 55% (P<0.001). Inhibition of miR-146b reduced the expression of IL-6 by 49% (P<0.001). Inhibition of miR-155 reduced the expression of IL-6 and IL-8 by respective 31% (P<0.001) and 14%. The inhibition of miR-146a, miR-146b, and miR-155 reduced the release of HSP10 by 50%, 35%, and 69% (P<0.05), respectively, but did not influence the expression of HSP27 or TXA2. In conclusion, miR-146a, miR-146b, and miR-155 are exerting anti-inflammatory properties by down-regulating IL-6 and IL-8, and influencing the expression of HSP10 in the activated endothelium. We provide evidence for the central role of selected miRNAs in sepsis and their use in the development of small interfering RNA therapeutics to target immune cells and sepsis pathways.

Indexed as

Cells, CulturedChaperonin 10Culture Media, ConditionedHumansInterleukin-6Interleukin-8In Vitro TechniquesMicroRNAsSepsisChaperonin 10Culture Media, ConditionedInterleukin-6Interleukin-8MicroRNAsMIRN146 microRNA, humanMIRN155 microRNA, human

Identifiers

PMID28662100
PMCPMC5491059
OpenAlexW2724255449

What OpenQuestion holds

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LicenceCC BY
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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.