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基因芯片筛选食管鳞癌患者癌及癌旁组织差异表达基因[J]. 肿瘤防治研究, 2009, 36(01): 17-20. DOI: 10.3971/j.issn.1000-8578.2009.01.005
引用本文: 基因芯片筛选食管鳞癌患者癌及癌旁组织差异表达基因[J]. 肿瘤防治研究, 2009, 36(01): 17-20. DOI: 10.3971/j.issn.1000-8578.2009.01.005
Screening Gene Expression Profiles of both Esophageal Squamous Cell Carcinoma Tissues and Adjacent Almost Normal Tissues by Microarray Screening Gene Expression Profiles of both Esophageal Squamous Cell Carcinoma Tissues and Adjacent Almost Normal Tissues by Microarray[J]. Cancer Research on Prevention and Treatment, 2009, 36(01): 17-20. DOI: 10.3971/j.issn.1000-8578.2009.01.005
Citation: Screening Gene Expression Profiles of both Esophageal Squamous Cell Carcinoma Tissues and Adjacent Almost Normal Tissues by Microarray Screening Gene Expression Profiles of both Esophageal Squamous Cell Carcinoma Tissues and Adjacent Almost Normal Tissues by Microarray[J]. Cancer Research on Prevention and Treatment, 2009, 36(01): 17-20. DOI: 10.3971/j.issn.1000-8578.2009.01.005

基因芯片筛选食管鳞癌患者癌及癌旁组织差异表达基因

Screening Gene Expression Profiles of both Esophageal Squamous Cell Carcinoma Tissues and Adjacent Almost Normal Tissues by Microarray Screening Gene Expression Profiles of both Esophageal Squamous Cell Carcinoma Tissues and Adjacent Almost Normal Tissues by Microarray

  • 摘要: 目的 探讨食管鳞癌(ESCC)患者癌组织基因表达谱。 方法 取3例无ESCC家族史的癌及癌旁组织等量混合,抽提RNA,将RNA逆转录合成相应cDNA,以Cy5和Cy3标记cDNA作为探针,在含有14 000点人类基因组芯片(BiostarH-140s)上进行杂交。用Scanarray 4000扫描仪扫描芯片荧光信号图像,用GenePix Pro 3.0软件对扫描图像进行数字化处理和分析。结果 依Ratio(cy5/cy3)>2.0或<0.5的数据项为差异表达的基因共1 855个。含表达序列标签(EST)844个,下调基因378个,上调基因466个。在1 011个已知功能的基因中,下调基因560个,上调基因451个。包含各类功能基因。同时与6例具有家族史ESCC组织差异基因进行了初步分析。经与NCBI基因库比对,有8个基因相同,且异常表达这与报道相符。 结论 基因芯片是一高效筛选食管癌相关基因的方法。在ESCC的发生、发展中存在着大量异常表达基因。

     

    Abstract: Objective To investigate the difference of gene expression profile in esophageal squamous cell carcinoma tissues (ESCC) and their adjacent almost normal tissues. Methods The cDNA retro–transcribed from 3 cases mRNA,which consisted of equal quantity of both ESCC and adjacent almost normal tissues,was labeled with Cy5 and Cy3 fluorescence as a probes. The mixed probes were hybridized with a piece of Biostar H-140s single dot human whole gene chip. The fluorescent signal was scanned by scanarray 4 000 instrument. The acquired image was analyzed by Genepix Pro 3.0 software. Results In 1 855 genes,whose Cy5/Cy3 ratios were greater than 2 or less than 0.5. There were 844 expressed sequence tags(ESTs), including 378 down-regulated genes and 466 up-regulated genes.On the other hand, among the 1 011 genes, which were acquired from genebank, included 560 down-regulated genes and 451 up-regulated genes.In the meantime, compared with the profiles from 6 cases of ESCC with family history,there were 8 of the 1 011 genes identical to the Genebank,and the expression of the 8 genes were same as the report as well. Conclusion Using the microarray to detect the difference of gene expression profiles might be of benefit to rapid select the relative genes of the esophageal carcinoma. There are lots of genes involved in the progression of ESCC.

     

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