Evidence map›Paper›PMID 34070455›Full record

ArticleInternational journal of molecular sciences2021

Tumor Suppressive Role of miR-342-5p in Human Chondrosarcoma Cells and 3D Organoids.

Clément Veys, Abderrahim Benmoussa, Romain Contentin, Amandine Duchemin, Emilie Brotin, Jérôme E Lafont, Yannick Saintigny, Laurent Poulain, Christophe Denoyelle, Magali Demoor and 2 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

17 citing papers in PubMed, 24 citations in OpenAlex.

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  8. siRNA Therapeutics: From Bench Lab. to Clinics.Pharmaceuticals (Basel, Switzerland) · 2024
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  16. Organoids: A New Chapter in Sarcoma Diagnosis and Treatment.International journal of molecular sciences · 2022
    Review
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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

12 authors at 4 institutions in 2 countries.

Clément VeysNormandie Univ, UNICAEN, BIOTARGEN, 14000 Caen, France.
Abderrahim BenmoussaNormandie Univ, UNICAEN, BIOTARGEN, 14000 Caen, France.ORCID 0000-0002-9504-3120
Romain ContentinNormandie Univ, UNICAEN, BIOTARGEN, 14000 Caen, France.ORCID 0000-0001-5917-7298
Amandine DucheminNormandie Univ, UNICAEN, BIOTARGEN, 14000 Caen, France.
Emilie BrotinNormandie Univ, UNICAEN, ImpedanCELL Platform, Federative Structure 4206 ICORE, 14000 Caen, France.
Jérôme E LafontCNRS UMR 5305, Laboratory of Tissue Biology and Therapeutic Engineering, Université Claude Bernard Lyon 1, Univ Lyon, 69367 Lyon, France.ORCID 0000-0001-8313-9873
Yannick SaintignyLARIA, iRCM, François Jacob Institute, DRF-CEA, 14000 Caen, France.ORCID 0000-0002-3839-3562
Laurent PoulainNormandie Univ, UNICAEN, INSERM U1086 ANTICIPE, Biology and Innovative Therapeutics for Ovarian Cancer (BioTICLA), 14000 Caen, France.ORCID 0000-0003-2241-3466
Christophe DenoyelleNormandie Univ, UNICAEN, ImpedanCELL Platform, Federative Structure 4206 ICORE, 14000 Caen, France.
Magali DemoorNormandie Univ, UNICAEN, BIOTARGEN, 14000 Caen, France.ORCID 0000-0002-8975-7055
Florence LegendreNormandie Univ, UNICAEN, BIOTARGEN, 14000 Caen, France.
Philippe GaléraNormandie Univ, UNICAEN, BIOTARGEN, 14000 Caen, France.ORCID 0000-0002-7797-2284
Normandie Université · FRInserm · FRCentre National de la Recherche Scientifique · FRUniversité Claude Bernard Lyon 1 · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chondrosarcomas are malignant bone tumors. Their abundant cartilage-like extracellular matrix and their hypoxic microenvironment contribute to their resistance to chemotherapy and radiotherapy, and no effective therapy is currently available. MicroRNAs (miRNAs) may be an interesting alternative in the development of therapeutic options. Here, for the first time in chondrosarcoma cells, we carried out high-throughput functional screening using impedancemetry, and identified five miRNAs with potential antiproliferative or chemosensitive effects on SW1353 chondrosarcoma cells. The cytotoxic effects of miR-342-5p and miR-491-5p were confirmed on three chondrosarcoma cell lines, using functional validation under normoxia and hypoxia. Both miRNAs induced apoptosis and miR-342-5p also induced autophagy. Western blots and luciferase reporter assays identified for the first time Bcl-2 as a direct target of miR-342-5p, and also Bcl-xL as a direct target of both miR-342-5p and miR-491-5p in chondrosarcoma cells. MiR-491-5p also inhibited EGFR expression. Finally, only miR-342-5p induced cell death on a relevant 3D chondrosarcoma organoid model under hypoxia that mimics the in vivo microenvironment. Altogether, our results revealed the tumor suppressive activity of miR-342-5p, and to a lesser extent of miR-491-5p, on chondrosarcoma lines. Through this study, we also confirmed the potential of Bcl-2 family members as therapeutic targets in chondrosarcomas.

Indexed as

Antineoplastic AgentsApoptosisAutophagybcl-X ProteinBone NeoplasmsCell CycleCell HypoxiaCell Line, TumorCell ProliferationChondrocytesChondrosarcomaCisplatinErbB ReceptorsHigh-Throughput Nucleotide SequencingHumansMicroRNAsAntineoplastic AgentsBCL2L1 protein, humanBCL2 protein, humanbcl-X ProteinCisplatinEGFR protein, humanErbB ReceptorsMicroRNAsMIRN342 microRNA, humanMIRN491 microRNA, humanProto-Oncogene Proteins c-bcl-2apoptosisautophagyBcl-2/Bcl-xLchondrosarcomamiR-342-5pmiR-491-5p

Identifiers

PMID34070455
PMCPMC8197525
OpenAlexW3165217867

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.