基础医学与临床 ›› 2009, Vol. 29 ›› Issue (12): 1277-1281.

• 研究论文 • 上一篇    下一篇

与原发性食管癌进展相关基因的筛选

李沛 凌志强 杨洪艳 赵继敏 黄幼田 赵明耀 董子明   

  1. 郑州大学基础医学院 Shiga University of Medical Science, JAPAN 郑州大学基础医学院 郑州大学基础医学院 郑州大学基础医学院 郑州大学基础医学院
  • 收稿日期:2008-12-25 修回日期:2009-03-26 出版日期:2009-12-20 发布日期:2009-12-20
  • 通讯作者: 李沛

Screening of the target genes related to the development and progression of ESCC

Pei LI, Zhi-qiang LING, Hong-yan YANG, Ji-min ZHAO, You-tian HUANG, Ming-yao ZHAO, Zi-ming DONG   

  1. College of Medical Sciences, Zhengzhou University Shiga University of Medical Science, JAPAN Basic Medical College, Zhengzhou University
  • Received:2008-12-25 Revised:2009-03-26 Online:2009-12-20 Published:2009-12-20
  • Contact: Pei LI,

摘要: 目的 应用基因微矩阵技术分析原发性食管癌基因表达谱,筛选与食管癌进展相关基因。方法 利用激光捕获微切割-T7 RNA聚合酶体外扩增联合cDNA芯片技术对15例原发性食管癌的基因表达谱进行筛选,并通过比较组间差异基因筛选出与肿瘤进展相关的基因。结果 在886条目的基因中,筛选出34条基因在Ⅰ/Ⅱ和Ⅲ/Ⅳ组间存在显著性差异(p<0.05),其中细胞周期调节类基因与早期食管癌发生有关,而细胞外基质类、黏附分子类基因主要参与食管癌的浸润和转移。结论 多个基因表达变化在食管癌发生中起作用,而进展相关基因的筛选为其临床诊治提供了新的思路和线索。

关键词: 食管癌, 基因芯片, 差异表达, 基因表达谱

Abstract: OBJECTIVE: This study was to investigate the differentially expressed genes between primary esophageal squamous cell carcinoma and normal esophageal mucosa using cDNA microarray. METHOD: LCM-GMA-cDNA microarray was used to detect the mRNA from both the primary carcinoma and the corresponding esophageal epithelium in 15 cases of human esophageal squamous cell carcinoma (ESCC). After high-stringent washing, the cDNA microarray was scanned for the fluorescent signals and showed differences between 2 tissues. RESULTS: Among the 886 target genes, 34 genes had significant differed between the Ⅰ/Ⅱand Ⅲ/Ⅳ group. Cell cycle regulators possibly promoting the growth of tumor cells were highly expressed in the early stages of ESCC, whereas adhesion molecules and extracellular matrix-related molecules possibly promoting invasiveness increased in the later stages. CONCLUSION: More than one gene contributed to esophageal cancer and the profiles of genes expression will open up new possibilities for understanding the molecular mechanism of tumor progression and be helpful to clinical treatment.

Key words: esophageal squamous cell carcinoma (ESCC), cDNA microarray, differential expression, gene expression profile

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