Evidence map›Paper›PMID 23921681›Full record

ArticleInternational journal of molecular sciences2013

MicroRNA expression changes during interferon-beta treatment in the peripheral blood of multiple sclerosis patients.

Michael Hecker, Madhan Thamilarasan, Dirk Koczan, Ina Schröder, Kristin Flechtner, Sherry Freiesleben, Georg Füllen, Hans-Jürgen Thiesen, Uwe Klaus Zettl

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed, 1 pooled it
5.2field-weighted citation impact, top 4% 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

58 citing papers in PubMed, 1 synthesis or guideline pooled it, 125 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. miRNA Signature in CSF From Patients With Primary Progressive Multiple Sclerosis.Neurology(R) neuroimmunology & neuroinflammation · 2023
    Article
  12. Review
  13. Review
  14. [Role of circular RNAs in immune-related diseases].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2022
    Review
  15. Article
  16. Review
  17. The role of miR-29 family in disease.Journal of cellular biochemistry · 2021
    Review
  18. Article
  19. Effects of therapeutic probiotics on modulation of microRNAs.Cell communication and signaling : CCS · 2021
    Review
  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

9 authors at 2 institutions in 1 country.

Michael HeckerSteinbeis Transfer Center for Proteome Analysis, Schillingallee 68, 18057 Rostock, Germany. michael.hecker@rocketmail.com
Madhan Thamilarasan
Dirk Koczan
Ina Schröder
Kristin Flechtner
Sherry Freiesleben
Georg Füllen
Hans-Jürgen Thiesen
Uwe Klaus Zettl
University of Rostock · DESteinbeis Foundation · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (miRNAs) are small non-coding RNA molecules acting as post-transcriptional regulators of gene expression. They are involved in many biological processes, and their dysregulation is implicated in various diseases, including multiple sclerosis (MS). Interferon-beta (IFN-beta) is widely used as a first-line immunomodulatory treatment of MS patients. Here, we present the first longitudinal study on the miRNA expression changes in response to IFN-beta therapy. Peripheral blood mononuclear cells (PBMC) were obtained before treatment initiation as well as after two days, four days, and one month, from patients with clinically isolated syndrome (CIS) and patients with relapsing-remitting MS (RRMS). We measured the expression of 651 mature miRNAs and about 19,000 mRNAs in parallel using real-time PCR arrays and Affymetrix microarrays. We observed that the up-regulation of IFN-beta-responsive genes is accompanied by a down-regulation of several miRNAs, including members of the mir-29 family. These differentially expressed miRNAs were found to be associated with apoptotic processes and IFN feedback loops. A network of miRNA-mRNA target interactions was constructed by integrating the information from different databases. Our results suggest that miRNA-mediated regulation plays an important role in the mechanisms of action of IFN-beta, not only in the treatment of MS but also in normal immune responses. miRNA expression levels in the blood may serve as a biomarker of the biological effects of IFN-beta therapy that may predict individual disease activity and progression.

Indexed as

Adaptor Proteins, Signal TransducingAdultApoptosisApoptosis Regulatory ProteinsCarrier ProteinsDown-RegulationFemaleGene Expression RegulationGenetic MarkersHumansInterferon-betaIntracellular Signaling Peptides and ProteinsLeukocytes, MononuclearMaleMicroRNAsMiddle AgedAdaptor Proteins, Signal TransducingApoptosis Regulatory ProteinsCarrier ProteinsGenetic MarkersInterferon-betaIntracellular Signaling Peptides and ProteinsMicroRNAsMIRN29a microRNA, humanNeoplasm ProteinsSH3BGRL2 protein, humanXAF1 protein, human

Identifiers

PMID23921681
PMCPMC3759901
OpenAlexW1980360288

What OpenQuestion 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 OpenQuestion graph.