Evidence map›Paper›PMID 29063445›Full record

ArticleJournal of molecular neuroscience : MN2017

IL-17 Exerts Anti-Apoptotic Effect via miR-155-5p Downregulation in Experimental Autoimmune Encephalomyelitis.

Dominika Ksiazek-Winiarek, Piotr Szpakowski, Malgorzata Turniak, Janusz Szemraj, Andrzej Glabinski

Open access · hybridAbstract read
In one paragraph

Article in Journal of molecular neuroscience : MN, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 2 pooled it
1.8field-weighted citation impact, top 13% 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

18 citing papers in PubMed, 2 syntheses or guidelines pooled it, 28 citations in OpenAlex.

  1. Pooled it
  2. Role of miR-155 in inflammatory autoimmune diseases: a comprehensive review.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2022
    Pooled it
  3. Review
  4. Article
  5. Review
  6. Cytokines and microRNAs in SARS-CoV-2: What do we know?Molecular therapy. Nucleic acids · 2022
    Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. Elevated IL-22 in psoriasis plays an anti-apoptotic role in keratinocytes through mediating Bcl-xL/Bax.Apoptosis : an international journal on programmed cell death · 2020
    Article
  15. Article
  16. Article
  17. Article
  18. 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

5 authors at 2 institutions in 1 country.

Dominika Ksiazek-WiniarekDepartment of Neurology and Stroke, Medical University of Lodz, Zeromskiego 113 Street, 90-549, Lodz, Poland. dominika.ksiazek@umed.lodz.pl.ORCID http://orcid.org/0000-0003-3366-333X
Piotr SzpakowskiDepartment of Neurology and Stroke, Medical University of Lodz, Zeromskiego 113 Street, 90-549, Lodz, Poland.
Malgorzata TurniakDepartment of Neurology and Stroke, Medical University of Lodz, Zeromskiego 113 Street, 90-549, Lodz, Poland.
Janusz SzemrajDepartment of Medical Biochemistry, Medical University of Lodz, Mazowiecka 6/8 Street, 92-215, Lodz, Poland.
Andrzej GlabinskiDepartment of Neurology and Stroke, Medical University of Lodz, Zeromskiego 113 Street, 90-549, Lodz, Poland.
Medical University of Lodz · PLLodz University of Technology · PL

Funding

Narodowe Centrum Nauki DEC-2012/05/N/NZ4/02347Uniwersytet Medyczny w Lodzi 503/5-062-01/503-51-002
6 · The paper itself

Abstract

Multiple sclerosis is an autoimmune, neurodegenerative disease, affecting mostly young adults and resulting in progressive disability. It is a multifactorial disorder, with important involvement of both cellular and epigenetic components. Among the epigenetic factors, microRNAs are currently intensively investigated in the context of multiple sclerosis. It has been shown that their biogenesis and function may be regulated by various cytokines. IL-17, a hallmark cytokine of Th17 cells, has been thought to function predominantly as a pro-inflammatory factor, leading to increased disease symptoms. However, there are several studies indicating its protective role during inflammatory process. In this work, we have assessed the impact of high-dose IL-17 administration on microRNAs' expression profile during the preclinical stage of EAE. For selected microRNA, we have performed computational analysis of its potential target mRNAs and cellular pathways. Based on results obtained from in silico analysis, we have chosen genes from neurotrophin signaling pathway for further experiments-BDNF, HRAS, and BCL2. Results obtained in this study suggested that high dose of IL-17 exerts protective activity via miR-155-5p downregulation. Increased expression of all studied genes, especially BCL2, indicated a potential anti-apoptotic function of IL-17 during the preclinical phase of EAE.

Indexed as

AnimalsApoptosisDown-RegulationEncephalomyelitis, Autoimmune, ExperimentalFemaleInterleukin-17MiceMicroRNAsNerve Growth FactorsSignal TransductionInterleukin-17MicroRNAsMirn155 microRNA, mouseNerve Growth FactorsBcl-2Experimental autoimmune encephalomyelitisInterleukin-17microRNAsMultiple sclerosis

Identifiers

PMID29063445
PMCPMC5696500
OpenAlexW2766856642

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.