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Identification of the differential expressive tumor associated genes in rectal cancers by cDNA microarray

机译:cDNA基因芯片鉴定直肠癌中差异表达的肿瘤相关基因

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AIM: To identify tumor associated genes of rectal cancer and to probe the application possibility of gene expression profiles for the classification of tumors. METHODS: Rectal cancer tissues and their paired normal mucosa were obtained from patients undergoing surgical resection of rectal cancer. Total RNA was extracted using Trizol reagents. First strand cDNA synthesis was indirectly labeled with aminoallyl-dUTP and coupled with Cy3 or Cy5 dye NHS mono-functional ester. After normalization to total spots, the genes which background subtracted intensity did not exceed 2 SD above the mean blank were excluded. The data were then sorted to obtain genes differentially expressed by ≥ 2 fold up or down in at least 5 of the 21 patients. RESULTS: In the 21 rectal cancer patients, 23 genes were up-regulated in at least 5 samples and 15 genes were down-regulated in at least 5 patients. Hierachical cluster analysis classified the patients into two groups according to the clinicopathological stage, with one group being all above stage Ⅱ and one group all below stage Ⅱ. CONCLUSION: The up-regulated genes and down-regulated genes may be molecular markers of rectal cancer. The expression profiles can be used for classification of rectal cancer.
机译:目的:鉴定直肠癌的肿瘤相关基因,并探讨基因表达谱在肿瘤分类中的应用可能性。方法:从接受直肠癌手术切除的患者中获取直肠癌组织及其配对的正常黏膜。用Trizol试剂提取总RNA。第一链cDNA合成用氨基烯丙基-dUTP间接标记,并与Cy3或Cy5染料NHS单官能酯偶联。归一化为总斑点后,排除背景扣除强度不超过平均空白的2 SD的基因。然后对数据进行分类以获得在21例患者中的至少5例中向上或向下≥2倍差异表达的基因。结果:在21例直肠癌患者中,至少5例样品中有23个基因被上调,而至少5例患者中有15个基因被下调。分级聚类分析根据临床病理阶段将患者分为两组,其中一组均在Ⅱ期以上,一组均在Ⅱ期以下。结论:上调基因和下调基因可能是直肠癌的分子标志物。表达谱可用于直肠癌的分类。

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