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作 者:李飞[1] 梁中锟[1] 荆玉明[1] 石小军[1] 陈三三[1] 万沛[1] 谭万龙[1]
机构地区:[1]南方医科大学南方医院泌尿外科,广州510515
出 处:《临床泌尿外科杂志》2011年第11期852-855,共4页Journal of Clinical Urology
基 金:广东省自然科学基金(编号9151051501000030)
摘 要:目的:从分子水平探讨膀胱癌的发病机制,为临床诊疗提供新思路。方法:从公共基因芯片数据库(GEO)中下载人膀胱癌的相关基因芯片数据,使用BRB-ArrayTools软件对其进行分析,筛选差异基因;并利用GATHER工具进行生物信息学分析。结果:BRB分析发现122个差异表达基因,其中上调55个,下调67个;GATHER分析发现这些差异基因的功能主要集中在细胞的生理过程、细菌凝聚反应的诱导作用、Jak-STAT和Toll-like受体的信号通路及细胞因子相互作用等生物学过程。结论:利用生物信息学方法能有效分析基因芯片数据并获取内在信息,为确定膀胱癌的早期诊断标志与治疗靶点提供新的思路。Objective: To explore the molecular pathogenesis of bladder cancer, and provide novel means for clinical diagnosis and treatment of this malignancy. Methods:The data of whole genomic expression profiles of bladder cancers were obtained from GEO database. Differential genes were identified by BRB-Array Tools software, then using GATHER tool for bioinformatics analysis. Results:BRB analysis results showed there were 122 differentially expressed genes in bladder cancer, 55 up-regulated and 67 down-regulated. These bladder cancerrelated genes played essential roles in such important biological processes as Cellular physiological process, Induction of bacterial agglutination,Toll-like receptor and Jak-STAT signaling pathway,cytokine-eytokine receptor interaction. Conclusions: The use of bioinformatics to analyze microarray data can found an interaction network involved. These would offer new ideas for early diagnosis and treat target of bladder cancer.
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