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[利用人类全基因组寡核苷酸微阵列筛选结直肠癌中差异表达基因]

[Screening of differentially expressed genes in colorectal cancer using human whole genomic oligonucleotide microarrays].

作者信息

Xu Hong-min, Wang Qiang, Bai Xue-juan, Zhong Ding-rong, Cao Xiu-tang, Zhang Jin-Ping, Ding Yan-qing, Yao Kai-tai

机构信息

Institute of Cancer Research, Department of Pathology, Southern Medical University, Guangzhou 510515, China.

出版信息

Di Yi Jun Yi Da Xue Xue Bao. 2005 Sep;25(9):1109-13.

Abstract

OBJECTIVE

To screen the differentially expressed genes in human colorectal cancer (CRC) tissue.

METHODS

Affymetrix oligonucleotide microarrays HG-U133 representing 32,264 human genes including 19,308 known genes and 12,956 expressed sequence tags (ESTs) were used to detect the gene expressions of CRC tissue paired with normal mucosa tissue. The microarray findings were confirmed by real-time quantitative reverse transcriptase-polymerase chain reaction (FQ-PCR). The gene expression profiles were analyzed by intersection and complement, rank sum test and t test.

RESULTS

Totally 3,125 genes and ESTs expressed differentially were detected in normal and cancer tissues, consisting of 974 up-regulated and 2,151 down-regulated genes with 247 ESTs present in CRC tissue and absent in normal mucosa and 162 ESTs absent in CRC tissue but present in normal mucosa. A percent of 80.1% of the differentially expressed genes were not reported in the literatures.

CONCLUSION

The strategy of data mining provides a foundation for filtering molecular markers and interpreting molecular carcinogenesis of CRC.

摘要

目的

筛选人类结直肠癌(CRC)组织中差异表达的基因。

方法

使用代表32264个人类基因(包括19308个已知基因和12956个表达序列标签(EST))的Affymetrix寡核苷酸微阵列检测CRC组织及配对的正常黏膜组织的基因表达。通过实时定量逆转录聚合酶链反应(FQ-PCR)确认微阵列结果。通过交集和补集、秩和检验和t检验分析基因表达谱。

结果

在正常组织和癌组织中总共检测到3125个差异表达的基因和EST,其中974个基因上调,2151个基因下调,247个EST在CRC组织中存在而在正常黏膜中不存在,162个EST在CRC组织中不存在但在正常黏膜中存在。80.1%的差异表达基因在文献中未被报道。

结论

数据挖掘策略为筛选CRC分子标志物和解释其分子致癌机制提供了基础。

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