Micro-RNA profiles in osteosarcoma as a predictive tool for ifosfamide response
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 authorDaniel Pissaloux
Service d'Anatomie et Cytologie Pathologiques, Centre Léon Bérard, 69373 Lyon cedex 08, France
Search for more papers by this authorAnthony Besse
Unité INSERM U590 équipe Cytokines et Cancer, Centre Léon Bérard, 69373 Lyon cedex 08, France
Search for more papers by this authorJennifer Perez
Unité INSERM U590 équipe Cytokines et Cancer, Centre Léon Bérard, 69373 Lyon cedex 08, France
Conticanet (FP6-06188)
Search for more papers by this authorAdeline Duc
Unité INSERM U590 équipe Cytokines et Cancer, Centre Léon Bérard, 69373 Lyon cedex 08, France
Conticanet (FP6-06188)
Search for more papers by this authorAurélie Dutour
Unité INSERM U590 équipe Cytokines et Cancer, Centre Léon Bérard, 69373 Lyon cedex 08, France
Conticanet (FP6-06188)
Search for more papers by this authorJean-Yves Blay
Unité INSERM U590 équipe Cytokines et Cancer, Centre Léon Bérard, 69373 Lyon cedex 08, France
Conticanet (FP6-06188)
EORTC, Brussels, Belgium
Search for more papers by this authorLaurent Alberti
Unité INSERM U590 équipe Cytokines et Cancer, Centre Léon Bérard, 69373 Lyon cedex 08, France
Conticanet (FP6-06188)
Search for more papers by this authorCorresponding 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 authorDaniel Pissaloux
Service d'Anatomie et Cytologie Pathologiques, Centre Léon Bérard, 69373 Lyon cedex 08, France
Search for more papers by this authorAnthony Besse
Unité INSERM U590 équipe Cytokines et Cancer, Centre Léon Bérard, 69373 Lyon cedex 08, France
Search for more papers by this authorJennifer Perez
Unité INSERM U590 équipe Cytokines et Cancer, Centre Léon Bérard, 69373 Lyon cedex 08, France
Conticanet (FP6-06188)
Search for more papers by this authorAdeline Duc
Unité INSERM U590 équipe Cytokines et Cancer, Centre Léon Bérard, 69373 Lyon cedex 08, France
Conticanet (FP6-06188)
Search for more papers by this authorAurélie Dutour
Unité INSERM U590 équipe Cytokines et Cancer, Centre Léon Bérard, 69373 Lyon cedex 08, France
Conticanet (FP6-06188)
Search for more papers by this authorJean-Yves Blay
Unité INSERM U590 équipe Cytokines et Cancer, Centre Léon Bérard, 69373 Lyon cedex 08, France
Conticanet (FP6-06188)
EORTC, Brussels, Belgium
Search for more papers by this authorLaurent Alberti
Unité INSERM U590 équipe Cytokines et Cancer, Centre Léon Bérard, 69373 Lyon cedex 08, France
Conticanet (FP6-06188)
Search for more papers by this authorAbstract
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.
Supporting Information
Additional Supporting Information may be found in the online version of this article.
Filename | Description |
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IJC_25715sm_suppfig1.tif481.6 KB | Supporting Figure 1 Reliability of TLDA technology for miRNA quantitation. A. 3D Scatter plot analysis of tumour (Tum), bone, muscle (Mus) and lung samples. B. Spearman's correlation between all pairs of samples. Heatmap showed that two samples from one tissue clustered together (red bars). |
IJC_25715sm_suppfig2.tif334 KB | Supporting Figure 2 The discriminating miRNAs interfered with Wnt and TGFβ pathways. Proteins in yellow, orange and red colours represent targets of miRNAs; a yellow square represents a weak repression while red represents the maximal repression; green squares were not targeted. A: human osteosarcoma; B: rat osteosarcoma. |
IJC_25715sm_suppfig3.tif62.3 KB | Supporting Figure 3 Barplot representation of discriminating miRNA expression in poor responders as compared to bad responders. Each miRNA was represented as the mean value for each group (bad vs good response) ± SEM = SD/√number of patients. |
IJC_25715sm_supptable1.doc62 KB | Supporting Table 1 Schedule of rat treatment. Ten rats bearing osteosarcoma tumours were randomly separated in two groups, one untreated (no in column 2) and one treated with ifosfamide 10mg/kg (yes) as described in materials and methods. Three types of response to ifosfamide were obtained: no response, medium response or high response. |
Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
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