Evidence map›Paper›PMID 27486986›Full record

ArticleOncotarget2016

miRNA-193a-5p repression of p73 controls Cisplatin chemoresistance in primary bone tumors.

Camille Jacques, Lidia Rodriguez Calleja, Marc Baud'huin, Thibaut Quillard, Dominique Heymann, François Lamoureux, Benjamin Ory

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
2.7field-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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

  1. Pooled it
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  5. Review
  6. Article
  7. miRNA signatures in childhood sarcomas and their clinical implications.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2019
    Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
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  16. Silencing of miR-193a-5p increases the chemosensitivity of prostate cancer cells to docetaxel.Journal of experimental & clinical cancer research : CR · 2017
    Article
  17. Review
  18. Review
  19. 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

7 authors at 2 institutions in 1 country.

Camille JacquesINSERM, UMR 957, Équipe Labellisée Ligue 2012, Nantes, France.
Lidia Rodriguez CallejaINSERM, UMR 957, Équipe Labellisée Ligue 2012, Nantes, France.
Marc Baud'huinINSERM, UMR 957, Équipe Labellisée Ligue 2012, Nantes, France.
Thibaut QuillardINSERM, UMR 957, Équipe Labellisée Ligue 2012, Nantes, France.
Dominique HeymannINSERM, UMR 957, Équipe Labellisée Ligue 2012, Nantes, France.
François LamoureuxINSERM, UMR 957, Équipe Labellisée Ligue 2012, Nantes, France.
Benjamin OryINSERM, UMR 957, Équipe Labellisée Ligue 2012, Nantes, France.
Nantes Université · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteosarcoma and Ewing Sarcoma are the two most common types of Bone Sarcomas, principally localized at the long bones of the extremities and mainly affecting adolescents and young adults. Cisplatin is one of the current options in the therapeutic arsenal of drugs available to cure these aggressive cancers. Unfortunately, chemoresistance against this agent is still a major cause of patient relapse. Thus, a better understanding of the molecular pathways by which these drugs induce cancer cell death, together with a better delineation of the origins of chemoresistance are required to improve the success rate of current treatments. Furthermore, as p53 is frequently mutated in Bone Sarcomas, other pathways in these cancers must mediate drug-induced cell death. Here, we demonstrate for the first time that TAp73β, a p53-family protein, is implicated in Cisplatin-induced apoptosis of Bone Sarcomas'. Furthermore, while acquired resistance developed by cancer cells against such drugs can have multiple origins, it is now well accepted that epigenetic mechanisms involving microRNAs (miRNAs) are one of them. We show that miRNA-193a-5p modulates the viability, the clonogenic capacity and the Cisplatin-induced apoptosis of the Bone Sarcoma cells through inhibition of TAp73β. Collectively, these results shed light on the involvement of miR-193a-5p in Cisplatin chemoresistance of Bone Sarcomas', and they open the road to new therapeutic opportunities provided by targeting the miR-193a-5p/TAp73β axis in the context of these malignancies.

Indexed as

Antineoplastic AgentsBone NeoplasmsCell Line, TumorCisplatinDrug Resistance, NeoplasmHumansMicroRNAsOsteosarcomaTumor Protein p73Tumor Suppressor Protein p53Antineoplastic AgentsCisplatinMicroRNAsMIRN193 microRNA, humanTP53 protein, humanTP73 protein, humanTumor Protein p73Tumor Suppressor Protein p53chemoresistancemicroRNAsp73

Identifiers

PMID27486986
PMCPMC5342358
OpenAlexW2500398980

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.