Evidence map›Paper›PMID 32380791›Full record

ArticleCells2020

hsa-miR-20b-5p and hsa-miR-363-3p Affect Expression of

Monika Drobna, Bronisława Szarzyńska, Roman Jaksik, Łukasz Sędek, Anna Kuchmiy, Tom Taghon, Pieter Van Vlierberghe, Tomasz Szczepański, Michał Witt, Małgorzata Dawidowska

Open access · goldAbstract read
In one paragraph

Article in Cells, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.0field-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

25 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Article
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  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Overview of miR-106a Regulatory Roles: from Cancer to Aging.Bioengineering (Basel, Switzerland) · 2023
    Review
  12. MiRNAs in Hematopoiesis and Acute Lymphoblastic Leukemia.International journal of molecular sciences · 2023
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. 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

10 authors at 4 institutions in 2 countries.

Monika DrobnaInstitute of Human Genetics Polish Academy of Sciences, 60-479 Poznań, Poland.
Bronisława SzarzyńskaInstitute of Human Genetics Polish Academy of Sciences, 60-479 Poznań, Poland.
Roman JaksikDepartment of Systems Biology and Engineering, Silesian University of Technology, 44-100 Gliwice, Poland.
Łukasz SędekDepartment of Microbiology and Immunology, Zabrze, Medical University of Silesia in Katowice, 41-808 Zabrze, Poland.
Anna KuchmiyDepartment of Diagnostic Sciences, Ghent University, 9000 Ghent, Belgium.
Tom TaghonDepartment of Diagnostic Sciences, Ghent University, 9000 Ghent, Belgium.
Pieter Van VlierbergheCancer Research Institute Ghent (CRIG), 9000 Ghent, Belgium.
Tomasz SzczepańskiDepartment of Pediatric Hematology and Oncology, Zabrze, Medical University of Silesia in Katowice, 41-800 Zabrze, Poland.
Michał WittInstitute of Human Genetics Polish Academy of Sciences, 60-479 Poznań, Poland.
Małgorzata DawidowskaInstitute of Human Genetics Polish Academy of Sciences, 60-479 Poznań, Poland.
Institute of Human Genetics · PLGhent University · BEMedical University of Silesia · PLSilesian University of Technology · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

T-cell acute lymphoblastic leukemia (T-ALL) is an aggressive malignancy arising from T lymphocyte precursors. We have previously shown by miRNA-seq, that miRNAs from the mir-106a-363 cluster are overexpressed in pediatric T-ALL. In silico analysis indicated their potential involvement in the regulation of apoptosis. Here, we aimed to test the hypothesis on the pro-tumorigenic roles of these miRNAs in T-ALL cells in vitro. We demonstrate, for the first time, that hsa-miR-20b-5p and hsa-miR-363-3p from the mir-106a-363 cluster, when upregulated in T-ALL cells in vitro, protect leukemic cells from apoptosis, enhance proliferation, and contribute to growth advantage. We show, using dual luciferase reporter assays, Ago2-RNA immunoprecipitation, RT-qPCR, and Western blots, that the oncogenic effects of these upregulated miRNAs might, at least in part, be mediated by the downregulation of two important tumor suppressor genes,

Indexed as

Gene Expression Regulation, NeoplasticGenes, Tumor SuppressorApoptosisBcl-2-Like Protein 11Cell Line, TumorCell ProliferationDown-RegulationHEK293 CellsHumansMicroRNAsPrecursor T-Cell Lymphoblastic Leukemia-LymphomaPTEN PhosphohydrolaseBcl-2-Like Protein 11MicroRNAsMIRN20b microRNA, humanMIRN363 microRNA, humanPTEN PhosphohydrolasePTEN protein, humanacute lymphoblastic leukemiamiRNA clusternoncoding RNAs in canceroncogenic miRNAssilencing tumor suppressor genes

Identifiers

PMID32380791
PMCPMC7290785
OpenAlexW3023555592

What OpenQuestion holds

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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.