Moriya Tetsuhiro, Seki Naohiko, Shimada Ken, Kato Masaki, Yakushiji Takashi, Nimura Yoshinori, Uzawa Katsuhiro, Takiguchi Masaki, Tanzawa Hideki
Department of Clinical Molecular Biology, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba 260-8670, Japan.
Int J Mol Med. 2003 Oct;12(4):429-35.
To analyze gene expression in oral cancer, we produced a specialized in-house cDNA microarray. The cDNA library was constructed from surgical specimens of oral squamous cell carcinoma (SCC) using an oligo-capping method. cDNA clones (n=4,800) were randomly selected and their 5'-end nucleotide sequences were determined. Overlapping clones were excluded, and 1,423 independent clones were selected and used for microarray production. Compared to the public nucleotide sequence database, 61% of our cDNA clones were full-length. By correlating expression patterns across SCC cell lines, we identified 53 genes (7 up-regulated and 46 down-regulated) that are differentially expressed in SCC cell lines compared to normal mucosa. Semi-quantitative RT-PCR analysis confirmed these findings and validity of our cDNA microarray. Using specimens from SCC patients, we investigated the expression status of the IL-1ra gene, which showed the down-regulated gene by microarray analysis. Gene expression clearly fell in the SCC specimens relative to their references, which indicated that our in-house cDNA microarray system rapidly identified and characterized candidate biomarkers for clinical use.
为了分析口腔癌中的基因表达,我们制作了一种专门的内部cDNA微阵列。cDNA文库是使用寡聚帽法从口腔鳞状细胞癌(SCC)的手术标本构建的。随机选择cDNA克隆(n = 4,800)并确定其5'端核苷酸序列。排除重叠克隆,选择1,423个独立克隆用于微阵列生产。与公共核苷酸序列数据库相比,我们61%的cDNA克隆是全长的。通过关联SCC细胞系中的表达模式,我们鉴定出53个基因(7个上调和46个下调),这些基因在SCC细胞系中与正常黏膜相比差异表达。半定量RT-PCR分析证实了这些发现以及我们cDNA微阵列的有效性。使用SCC患者的标本,我们研究了IL-1ra基因的表达状态,该基因在微阵列分析中显示为下调基因。相对于其对照,SCC标本中的基因表达明显下降,这表明我们的内部cDNA微阵列系统能够快速识别和表征临床使用的候选生物标志物。