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微阵列分析鉴定出人骨肉瘤中与组织学分型相关的独特基因表达谱。

Microarray analysis identifies distinct gene expression profiles associated with histological subtype in human osteosarcoma.

机构信息

Department of Orthopedics, Medical University of Vienna, Vienna, Austria.

出版信息

Int Orthop. 2011 Mar;35(3):401-11. doi: 10.1007/s00264-010-0996-6. Epub 2010 Mar 26.

Abstract

Osteosarcoma is the most common primary malignant bone tumour. Currently osteosarcoma classification is based on histological appearance. It was the aim of this study to use a more systematic approach to osteosarcoma classification based on gene expression analysis and to identify subtype specific differentially expressed genes. We analysed the global gene expression profiles of ten osteosarcoma samples using Affymetrix U133A arrays (five osteoblastic and five non-osteoblastic osteosarcoma patients). Differential gene expression analysis yielded 75 genes up-regulated and 97 genes down-regulated in osteoblastic versus non-osteoblastic osteosarcoma samples, respectively. These included genes involved in cell growth, chemotherapy resistance, angiogenesis, steroid- and neuropeptide hormone receptor activity, acute-phase response and serotonin receptor activity and members of the Wnt/ß-catenin pathway and many others. Furthermore, we validated the highly differential expression of six genes including angiopoietin 1, IGFBP3, ferredoxin 1, BMP, decorin, and fibulin 1 in osteoblastic osteosarcoma relative to non-osteoblastic osteosarcoma. Our results show the utility of gene expression analysis to study osteosarcoma subtypes, and we identified several genes that may play a role as potential therapeutic targets in the future.

摘要

骨肉瘤是最常见的原发性恶性骨肿瘤。目前,骨肉瘤的分类是基于组织学表现。本研究旨在采用更系统的方法,基于基因表达分析对骨肉瘤进行分类,并鉴定出具有特定亚型差异表达的基因。我们使用 Affymetrix U133A 阵列分析了 10 个骨肉瘤样本的全局基因表达谱(5 个成骨细胞性和 5 个非成骨细胞性骨肉瘤患者)。差异基因表达分析显示,成骨细胞性骨肉瘤与非成骨细胞性骨肉瘤样本相比,分别有 75 个基因上调和 97 个基因下调。这些基因包括参与细胞生长、化疗耐药、血管生成、甾体和神经肽激素受体活性、急性期反应和 5-羟色胺受体活性以及 Wnt/β-连环蛋白通路的许多其他成员。此外,我们验证了在成骨细胞性骨肉瘤中,包括血管生成素 1、IGFBP3、铁氧还蛋白 1、BMP、核心蛋白聚糖和纤维蛋白 1 在内的 6 个基因的高度差异表达,而在非成骨细胞性骨肉瘤中则无差异表达。我们的结果表明,基因表达分析可用于研究骨肉瘤亚型,并且我们鉴定出了一些可能在未来作为潜在治疗靶点发挥作用的基因。

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