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食管腺癌与Barrett's食管基因表达谱的研究[J]. 肿瘤防治研究, 2009, 36(08): 639-642. DOI: 10.3971/j.issn.1000-8578.2009.08.003
引用本文: 食管腺癌与Barrett's食管基因表达谱的研究[J]. 肿瘤防治研究, 2009, 36(08): 639-642. DOI: 10.3971/j.issn.1000-8578.2009.08.003
Correlation between Gene Expression Profile of Adenocarcinoma of Esophagus and Barrett's Esophagus[J]. Cancer Research on Prevention and Treatment, 2009, 36(08): 639-642. DOI: 10.3971/j.issn.1000-8578.2009.08.003
Citation: Correlation between Gene Expression Profile of Adenocarcinoma of Esophagus and Barrett's Esophagus[J]. Cancer Research on Prevention and Treatment, 2009, 36(08): 639-642. DOI: 10.3971/j.issn.1000-8578.2009.08.003

食管腺癌与Barrett's食管基因表达谱的研究

Correlation between Gene Expression Profile of Adenocarcinoma of Esophagus and Barrett's Esophagus

  • 摘要: 目的 探讨从Barrett's食管到食管腺癌的癌变过程中基因表达谱的变化。 方法 取同一食管腺癌患者大体手术标本经病理确诊的腺癌组织、Barrett's 食管组织及正常组织,分别提取组织上皮的总RNA并纯化mRNA;将mRNA逆转录合成以Cy5和Cy3标记的cDNA链做探针,分别混合后在两张基因表达谱芯片上进行杂交。用扫描仪扫描芯片荧光信号,用软件对扫描图像进行分析。 结果 食管腺癌与正常食管上皮比较差异2倍以上共有214个基因;Barrett's食管与正常食管上皮比较差异2倍以上共有90个基因。而Barrett's食管组织和食管腺癌组织均下调的基因有24个,均上调的基因有21个。其中符合从Barrett's食管到食管腺癌演变趋势的基因中,上调的有9个,下调的有18个。 结论 这些基因或其产物可作为Barrett's食管具有癌变高危性的检测指标

     

    Abstract: Objective To investigate the characteristics of genic changes from Barrett's esophagus to esophageal adenocarcinoma by cDNA microarray. Methods The cDNA as probe marked by Cy3 and Cy5 was reverse transcription from equal quantity mRNA of esophageal carcinoma and Barrett's esophagus tissues and control normal esophageal epithelium which were all from one patient with esophageal adenocarcinoma. The mixed probes were hybridized with two pieces gene chip respectively. It was scanned by laser scanner ScanArray4000. The acquired images were analyzed by software GenePix Pro3.0. Results A total of 214 genes were screened out which transcriptional levels were 2 times in hybridization of esophageal adenocarcinoma than normal esophageal epithelium,whereas 90 genes in hybridization of Barrett's esophagus compared with normal epithelium. A parallel comparison among these two gene profiles showed that 45 genes with 24 downregulation and 21 upregulation which transcriptional levels were more than 2 times between the Barrett's esophagus and the esophageal adenocarcinoma. Among these, there were 27 genes with 18 downregulation and 9 upregulation which corresponded with the tendencies of progress from Barrett's esophagus to esophageal adenocarcinoma. Conclusion These genes or their products which implicates the tendencies can be choosen as indicators of carcinogenesis with high risk index of Barrett's esophagus.

     

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