Volume 129, Issue 3 pp. 680-690
Early Detection and Diagnosis

Micro-RNA profiles in osteosarcoma as a predictive tool for ifosfamide response

Angélique Gougelet

Corresponding Author

Angélique Gougelet

Unité INSERM U590 équipe Cytokines et Cancer, Centre Léon Bérard, 69373 Lyon cedex 08, France

Conticanet (FP6-06188)

Tel.: +33478782964, Fax: +33478782720

Unité INSERM U590 Cytokines et Cancer, Centre Léon Bérard, 28 rue Laennec, 69373 Lyon cedex 08, FranceSearch for more papers by this author
Daniel Pissaloux

Daniel Pissaloux

Service d'Anatomie et Cytologie Pathologiques, Centre Léon Bérard, 69373 Lyon cedex 08, France

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Anthony Besse

Anthony Besse

Unité INSERM U590 équipe Cytokines et Cancer, Centre Léon Bérard, 69373 Lyon cedex 08, France

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Jennifer Perez

Jennifer Perez

Unité INSERM U590 équipe Cytokines et Cancer, Centre Léon Bérard, 69373 Lyon cedex 08, France

Conticanet (FP6-06188)

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Adeline Duc

Adeline Duc

Unité INSERM U590 équipe Cytokines et Cancer, Centre Léon Bérard, 69373 Lyon cedex 08, France

Conticanet (FP6-06188)

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Aurélie Dutour

Aurélie Dutour

Unité INSERM U590 équipe Cytokines et Cancer, Centre Léon Bérard, 69373 Lyon cedex 08, France

Conticanet (FP6-06188)

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Jean-Yves Blay

Jean-Yves Blay

Unité INSERM U590 équipe Cytokines et Cancer, Centre Léon Bérard, 69373 Lyon cedex 08, France

Conticanet (FP6-06188)

EORTC, Brussels, Belgium

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Laurent Alberti

Laurent Alberti

Unité INSERM U590 équipe Cytokines et Cancer, Centre Léon Bérard, 69373 Lyon cedex 08, France

Conticanet (FP6-06188)

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First published: 14 October 2010
Citations: 111

Abstract

Micro-RNAs (miRNA) are currently used as cancer biomarkers for hematological cancers and solid tumors. Osteosarcoma is the first primary malignant bone tumor, characterized by a complex genetic and resistance to conventional treatments. For this latter property, the median survival has not been improved since 1990 despite preoperative administration of chemotherapeutic agents. The prediction of tumor response before chemotherapy treatment would constitute a major progress for this pathology. We assessed in this study if miRNA profiling could surpass the current limitations for osteosarcoma diagnosis. We measured the miRNA expression in different osteosarcoma samples: (i) 27 osteosarcoma paraffin-embedded tumors from patients, (ii) human osteosarcoma cell lines, and (iii) tumors from a syngeneic rat osteosarcoma model, recapitulating human osteosarcoma. miRNA profiles were determined using microfluidic cards performing high-throughput TaqMan®-based PCR assays, called TaqMan® Low Density Arrays. Osteosarcoma of rat and human origins showed a miRNA signature, which could discriminate good from bad responders. In particular, we identified five discriminating miRNAs (miR-92a, miR-99b, miR-132, miR-193a-5p and miR-422a) in patient tumors, which could be easily transferable to diagnosis. These discriminating miRNAs, as well as those identified in rat, targeted the TGFβ, the Wnt and the MAP kinase pathways. These results indicate that our platform constitutes a potent diagnostic tool to predict tumor sensitivity to a drug in attempt to better adapt treatment to tumor biological specificities and also to identify new potential therapeutic strategies.

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