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骨肉瘤中 microRNA 谱作为异环磷酰胺反应的预测工具。

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

机构信息

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

出版信息

Int J Cancer. 2011 Aug 1;129(3):680-90. doi: 10.1002/ijc.25715. Epub 2010 Nov 23.

DOI:10.1002/ijc.25715
PMID:20949564
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.

摘要

微小 RNA(miRNA)目前被用作血液系统癌症和实体瘤的癌症生物标志物。骨肉瘤是第一种原发性恶性骨肿瘤,其特征是遗传复杂且对常规治疗具有抗性。对于后者的特性,尽管术前给予化疗药物,自 1990 年以来,中位生存期并未得到改善。在化疗治疗前预测肿瘤反应将是该病理学的重大进展。我们在这项研究中评估了 miRNA 分析是否可以超越骨肉瘤诊断的当前局限性。我们测量了不同骨肉瘤样本中的 miRNA 表达:(i)来自患者的 27 个骨肉瘤石蜡包埋肿瘤,(ii)人骨肉瘤细胞系,和(iii)模拟人骨肉瘤的同种异体大鼠骨肉瘤模型中的肿瘤。使用微流体卡进行高通量 TaqMan(®)基于 PCR 的测定(称为 TaqMan(®)低密度阵列)来确定 miRNA 谱。大鼠和人类来源的骨肉瘤显示出 miRNA 特征,可区分良好和不良反应者。特别是,我们在患者肿瘤中鉴定了五个有区别的 miRNA(miR-92a、miR-99b、miR-132、miR-193a-5p 和 miR-422a),这些 miRNA 易于转移到诊断中。这些有区别的 miRNA 以及在大鼠中鉴定的 miRNA,靶向 TGFβ、Wnt 和 MAP 激酶途径。这些结果表明,我们的平台构成了一种强大的诊断工具,可预测肿瘤对药物的敏感性,试图更好地使治疗适应肿瘤的生物学特性,并确定新的潜在治疗策略。

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