Evidence map›Paper›PMID 33270982›Full record

ArticleJournal of cellular and molecular medicine2021

miR-15a-5p and miR-21-5p contribute to chemoresistance in cytogenetically normal acute myeloid leukaemia by targeting PDCD4, ARL2 and BTG2.

Virginie Vandewalle, Ahmed Essaghir, Emeline Bollaert, Sandrine Lenglez, Carlos Graux, Hélène Schoemans, Pascale Saussoy, Lucienne Michaux, Peter J M Valk, Jean-Baptiste Demoulin and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

31 citing papers in PubMed, 44 citations in OpenAlex.

  1. Review
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  6. MircoRNAs predict and modulate responses to chemotherapy in leukemic patients.Naunyn-Schmiedeberg's archives of pharmacology · 2025
    Review
  7. Apelin/APJ: Another Player in the Cancer Biology Network.International journal of molecular sciences · 2025
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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

11 authors at 5 institutions in 2 countries.

Virginie VandewalleDepartment of Hematology, Cliniques Universitaires Saint-Luc, Brussels, Belgium.
Ahmed EssaghirExperimental Medicine Unit, de Duve Institute, Université Catholique de Louvain, Brussels, Belgium.
Emeline BollaertExperimental Medicine Unit, de Duve Institute, Université Catholique de Louvain, Brussels, Belgium.
Sandrine LenglezExperimental Medicine Unit, de Duve Institute, Université Catholique de Louvain, Brussels, Belgium.
Carlos GrauxDepartment of Hematology, CHU UCL Namur (Godinne site), Yvoir, Belgium.
Hélène SchoemansDepartment of Hematology, University Hospitals Leuven and KU Leuven, Leuven, Belgium.
Pascale SaussoyLaboratory of Hematology, Cliniques Universitaires Saint Luc, Brussels, Belgium.
Lucienne MichauxCenter for Human Genetics, University Hospitals Leuven and KU Leuven, Leuven, Belgium.
Peter J M ValkDepartment of Hematology, Erasmus University Medical Center, Rotterdam, the Netherlands.
Jean-Baptiste DemoulinExperimental Medicine Unit, de Duve Institute, Université Catholique de Louvain, Brussels, Belgium.
Violaine HavelangeDepartment of Hematology, Cliniques Universitaires Saint-Luc, Brussels, Belgium.ORCID 0000-0001-6061-6315
de Duve Institute · BECliniques Universitaires Saint-Luc · BEKU Leuven · BECHU Dinant Godinne UCL Namur · BEErasmus MC · NL

Funding

Fondation Salus SanguinisFonds De La Recherche Scientifique - FNRSFonds MaisinKoning BoudewijnstichtingPlan Cancer Action#29Stichting Tegen Kanker
6 · The paper itself

Abstract

Cytarabine and daunorubicin are old drugs commonly used in the treatment of acute myeloid leukaemia (AML). Refractory or relapsed disease because of chemotherapy resistance is a major issue. microRNAs (miRNAs) were incriminated in resistance. This study aimed to identify miRNAs involved in chemoresistance in AML patients and to define their target genes. We focused on cytogenetically normal AML patients with wild-type NPM1 without FLT3-ITD as the treatment of this subset of patients with intermediate-risk cytogenetics is not well established. We analysed baseline AML samples by small RNA sequencing and compared the profile of chemoresistant to chemosensitive AML patients. Among the miRNAs significantly overexpressed in chemoresistant patients, we revealed miR-15a-5p and miR-21-5p as miRNAs with a major role in chemoresistance in AML. We showed that miR-15a-5p and miR-21-5p overexpression decreased apoptosis induced by cytarabine and/or daunorubicin. PDCD4, ARL2 and BTG2 genes were found to be targeted by miR-15a-5p, as well as PDCD4 and BTG2 by miR-21-5p. Inhibition experiments of the three target genes reproduced the functional effect of both miRNAs on chemosensitivity. Our study demonstrates that miR-15a-5p and miR-21-5p are overexpressed in a subgroup of chemoresistant AML patients. Both miRNAs induce chemoresistance by targeting three pro-apoptotic genes PDCD4, ARL2 and BTG2.

Indexed as

ApoptosisBlotting, WesternCell Line, TumorCytarabineDaunorubicinDrug Resistance, NeoplasmHumansLeukemia, Myeloid, AcuteMicroRNAsMutationNuclear ProteinsNucleophosminPrincipal Component AnalysisRNA, Small InterferingCytarabineDaunorubicinMicroRNAsMIRN15 microRNA, humanMIRN20b microRNA, humanNPM1 protein, humanNuclear ProteinsNucleophosminRNA, Small Interferingacute myeloid leukaemiaapoptosischemoresistancemicroRNAstarget genes

Identifiers

PMID33270982
PMCPMC7810923
OpenAlexW3108756598

What OpenQuestion holds

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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.