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作 者:曹磊[1] 纪方[1] 蔡晓冰[1] 唐昊[1] 竺伟[1] 张瑞[1]
机构地区:[1]第二军医大学长海医院,上海长海路200433
出 处:《中国矫形外科杂志》2009年第1期55-58,共4页Orthopedic Journal of China
基 金:上海市科委基金资助项目(编号:64119605)
摘 要:[目的]运用基因芯片技术探索骨肉瘤发病及转移相关基因,研究基因表达水平对于骨肉瘤发生及转移的重要意义。[方法]采用2个公认的骨肉瘤细胞株及1个成骨细胞株,提取总RNA,合成生物素标记的cRNA与SBC基因芯片杂交。随机挑选4个差异表达基因,分别设计合成引物,用嵌合荧光法(SYBR Green Ⅰ)实时RT-PCR法定量测量术中收集的新鲜骨肉瘤标本及两株细胞中各基因的表达水平,应用ABI Prism 7 300分析其与成骨细胞株之间的表达差异。[结果]以表达差异≥2.0或≤0.5倍为限,在SBC芯片包含的所有基因(约15 000个转录本)中,2个骨肉瘤细胞株与成骨细胞株相比较,共同上调189个基因;共同下调84个基因。随机挑选4个差异表达基因的实时RT-PCR结果与芯片结果完全相符。[结论]骨肉瘤是一种多基因病变,应用基因芯片技术有助于发现该肿瘤的基因变化规律。[ Objective I To investigation the relavant genes to the pathogenesis and metastasis of osteosarcoma, and to discuss the significance of gene expression in the pathogenesis and metastasis of osteosarcoma. [ Method] Two well - known ATCC osteosarcoma cell lines and an osteoblastic cell line were collected. After the total RNA was extracted, the finally synthesized biotinylated cRNAs were hybridized to SBC arrays. After the design and synthethesis of the primers, four of the differentially expressed genes were then chosen at random to further confirm the drray results using the SYBR Green real - time RT - PCR method in freshly collected osteosarcoma specimens and the cell lines. The data analysis depended on the ABI Prism 7300 system. [ Result] By an entrance limit of ≥12. 0 or ≤0. 5, 189 up- regulated and 84 dowm- regulated genes which were considerable differentially expressed in the two osteosarcoma cell lines compared with the osteoblastic cell line hfobl. 19 were finally detected. Many of the genes were first reported to be related to the pathogenesis of osteosarcoma. The array results were further confirmed by the real - time RT - PCR. [ Conclusion] Many genes are involved in the pathogenesis and metastasis of osteosarcoma. It is helpful to apply gene array to find the laws of gene expression and to study the gene - gene interactional relationships in this tumor.
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