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作 者:胡锦伟[1] 肖强[1] 谢玉波[2] 李雷[1] 王长青[1] 解乃昌[1]
机构地区:[1]广西医科大学第一附属医院胃肠腺体外科,南宁530021 [2]广西医科大学第一附属医院麻醉科
出 处:《广西医科大学学报》2009年第3期355-358,共4页Journal of Guangxi Medical University
基 金:国家自然科学基金资助项目(No.30860273);广西医疗卫生重点科研课题(桂卫重200844)
摘 要:目的:了解E2F-1过表达对胃癌细胞中癌基因和抑癌基因表达的影响,探讨E2F-1影响胃癌细胞侵袭能力的作用机制。方法:从胃癌细胞MGC-803和MGC-803/E2F-1中提取总RNA,纯化mRNA,逆转录将Cy3和Cy5两种荧光素标记到两组逆转录合成的第一链cDNA。与22K人类基因组寡核苷酸芯片进行杂交,采用LuxScan 10K/A双通道激光扫描仪扫描芯片上两种荧光信号,应用LuxScan3.0图像分析软件对图像处理分析,筛选出差异基因。结果:在21522条基因中,MGC-803/E2F-1和MGC-803细胞差异表达的癌基因和抑癌基因有39条,其中上调基因19条(49%),下调基因20条(51%)。结论:过表达E2F-1在胃癌细胞MGC-803中影响了众多癌基因和抑癌基因的表达变化,表明胃癌侵袭能力的变化是多基因相互作用,多种信号传导途径相互影响的结果。Objective: To investigate the differentially expression of oncogenes/anti-oncogenes in gastric cancer cell line ovrexpression of E2F-1 by gene chip technique, and fine the molecular mechanisms of oncogene and anti-oncogene effect on gastric cancer cell invasion capability. Methods:The total RNA was extracted from MGC-803/E2F-1 and MGC-803 gastric cancer cell line , then purified. The eDNA was obtained by reverse transcription polymerase chain reaction (RT-PCR), and then labeled with Cy3 and Cy5 fluorescence as probes, which were hybridized with gene chip containing 22 k human genome oligonucleotide. Subsequently, the two signal images were scanned by LuxScan 10K/A dual pathways laser scanner and analyzed by LuxScan 3.0 image analysis software,then screening out differentially expressed genes. Results: Of the 215222 target genes,39 oncogenes and anti-oncogenes were screened out for differences in gene expression level between gastric cancer cell line MGC-803/E2F-1 and MGC 803. Nineteen genes were up-regulated(49%)and 20 genes were down-regulated(51%). Conclusion : After ovrexpression E2F-1 in vitro, the gastric cancer cell line MGC-803 effects by multiple oncogenes/anti-oncogenes expression. Subsequently,invasion capability is the effect by multiple oncogenes/anti-oncogenes and regulation in multiple signal pathways.
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