Evidence map›Paper›PMID 25622103›Full record

ReviewOncotarget2015

MicroRNAs in B-cells: from normal differentiation to treatment of malignancies.

Sara Correia Marques, Maria Bach Laursen, Julie Støve Bødker, Malene Krag Kjeldsen, Steffen Falgreen, Alexander Schmitz, Martin Bøgsted, Hans Erik Johnsen, Karen Dybkaer

Open access · diamondAbstract readReview
In one paragraph

Review in Oncotarget, 2015. 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
1.2field-weighted citation impact, top 23% 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, 26 citations in OpenAlex.

  1. Review
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  3. Article
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  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Diagnostic and predictive biomarkers for lymphoma diagnosis and treatment in the era of precision medicine.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2016
    Review
  12. Review
  13. miR-155 as a Biomarker in B-Cell Malignancies.BioMed research international · 2016
    Review
  14. 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.

Sara Correia MarquesDepartment of Haematology, Aalborg University Hospital, Aalborg, Denmark. Department of Clinical Medicine, Aarhus University, Denmark.
Maria Bach LaursenDepartment of Haematology, Aalborg University Hospital, Aalborg, Denmark.
Julie Støve BødkerDepartment of Haematology, Aalborg University Hospital, Aalborg, Denmark.
Malene Krag KjeldsenDepartment of Haematology, Aalborg University Hospital, Aalborg, Denmark.
Steffen FalgreenDepartment of Haematology, Aalborg University Hospital, Aalborg, Denmark.
Alexander SchmitzDepartment of Haematology, Aalborg University Hospital, Aalborg, Denmark.
Martin BøgstedDepartment of Haematology, Aalborg University Hospital, Aalborg, Denmark. Department of Clinical Medicine, Aalborg University, Denmark.
Hans Erik JohnsenDepartment of Haematology, Aalborg University Hospital, Aalborg, Denmark. Department of Clinical Medicine, Aalborg University, Denmark. Clinical Cancer Research Center, Aalborg University Hospital, Denmark.
Karen DybkaerDepartment of Haematology, Aalborg University Hospital, Aalborg, Denmark. Department of Clinical Medicine, Aalborg University, Denmark.
Aalborg University Hospital · DKAalborg University · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (miRNAs) are small non-coding RNAs that play important post-transcriptional regulatory roles in a wide range of biological processes. They are fundamental to the normal development of cells, and evidence suggests that the deregulation of specific miRNAs is involved in malignant transformation due to their function as oncogenes or tumor suppressors. We know that miRNAs are involved in the development of normal B-cells and that different B-cell subsets express specific miRNA profiles according to their degree of differentiation. B-cell-derived malignancies contain transcription signatures reminiscent of their cell of origin. Therefore, we believe that normal and malignant B-cells share features of regulatory networks controlling differentiation and the ability to respond to treatment. The involvement of miRNAs in these processes makes them good biomarker candidates. B-cell malignancies are highly prevalent, and the poor overall survival of patients with these malignancies demands an improvement in stratification according to prognosis and therapy response, wherein we believe miRNAs may be of great importance. We have critically reviewed the literature, and here we sum up the findings of miRNA studies in hematological cancers, from the development and progression of the disease to the response to treatment, with a particular emphasis on B-cell malignancies.

Indexed as

Cell Transformation, NeoplasticBiomarkers, TumorB-LymphocytesCell DifferentiationDisease ProgressionDrug Resistance, NeoplasmGene Expression Regulation, NeoplasticGenes, Tumor SuppressorHematologic NeoplasmsHumansMicroRNAsNeoplasmsOncogenesTreatment OutcomeBiomarkers, TumorMicroRNAs

Identifiers

PMID25622103
PMCPMC4381575
OpenAlexW1878716376

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.