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Genome-wide screening of genes showing altered expression in liver metastases of human colorectal cancers by cDNA microarray
被引:80
|作者:
Yanagawa, R
Furukawa, Y
Tsunoda, T
Kitahara, O
Kameyama, M
Murata, K
Ishikawa, O
Nakamura, Y
机构:
[1] Univ Tokyo, Inst Med Sci, Ctr Human Genome, Mol Med Lab,Minato Ku, Tokyo 1088639, Japan
[2] RIKEN, SNP Res Ctr, Lab Med Informat, Minato Ku, Tokyo 1088639, Japan
[3] Osaka Med Ctr Canc & Cardiovasc Dis, Dept Surg Oncol, Higashinari Ku, Osaka 5378511, Japan
来源:
NEOPLASIA
|
2001年
/
3卷
/
05期
基金:
日本学术振兴会;
关键词:
metastasis;
cDNA microarray;
microdissection;
colorectal cancer (CRC);
T7-based RNA amplification;
D O I:
10.1038/sj.neo.7900185
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
In spite of intensive and increasingly successful attempts to determine the multiple steps involved in colorectal carcinogenesis, the mechanisms responsible for metastasis of colorectal tumors to the liver remain to be clarified. To identify genes that are candidates for involvement in the metastatic process, we analyzed genome-wide expression profiles of 10 primary colorectal cancers and their corresponding metastatic lesions by means of a cDNA microarray consisting of 9121 human genes. This analysis identified 40 genes whose expression was commonly upregulated in metastatic lesions, and 7 that were commonly downregulated. The upregulated genes encoded proteins involved in cell adhesion, or remodeling of the actin cytoskeleton. Investigation of the functions of more of the altered genes should improve our understanding of metastasis and may identify diagnostic markers and/or novel molecular targets for prevention or therapy of metastatic lesions.
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页码:395 / 401
页数:7
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