Colorectal Cancer
Copyright ©The Author(s) 2005. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Jul 28, 2005; 11(28): 4337-4343
Published online Jul 28, 2005. doi: 10.3748/wjg.v11.i28.4337
Effect of NS398 on metastasis-associated gene expression in a human colon cancer cell line
Xue-Qin Gao, Jin-Xiang Han, Hai-Yan Huang, Bao Song, Bo Zhu, Chang-Zheng Song
Xue-Qin Gao, Jin-Xiang Han, Hai-Yan Huang, Bao Song, Bo Zhu, Chang-Zheng Song, Key Laboratory of Ministry of Public Health for Biotech-Drug, Shandong Medicinal and Biotechnology Center, Shandong Academy of Medical Sciences, Jinan 250062, Shandong Province, China
Xue-Qin Gao, Jin-Xiang Han, Shandong University School of Medicine, Jinan 250062, Shandong Province, China
Author contributions: All authors contributed equally to the work.
Supported by the Key Technology Research and Development Program of Shandong Province, No. 011100105
Correspondence to: Professor Jin-Xiang Han, Shandong Medicinal and Biological Center, Shandong Academy of Medical Sciences, 89 Jingshi Road, Jinan 250062, Shandong Province, China. han9888@sina.com
Telephone: +86-531-82919888 Fax: +86-531-82951586
Received: September 8, 2004
Revised: December 1, 2004
Accepted: December 3, 2004
Published online: July 28, 2005
Abstract

AIM: To investigate the effect of NS398 on the metastasis-associated gene expression in LoVo colorectal cancer cells.

METHODS: LoVo cells were treated with NS398 at the concentration of 100 mmol/L for 24 and 48 h respectively. Total RNA was extracted with TRIzol reagents and reverse transcribed with Superscript II and hybridized with cDNA microarray (containing oncogenes, tumor suppressor genes, signal transduction molecules, adhesive molecules, growth factors, and ESTs) fabricated in our laboratory. After normalization, the ratio of gene expression of NS398 treated to untreated LoVo cells was either 2-fold up or 0.5-fold down was defined as the differentially expressed genes. Semi-quantitative RT-PCR was used to validate the microarray results.

RESULTS: Among the 447 metastasis-associated genes, 9 genes were upregulated and 8 genes were downregulated in LoVo cells treated with NS398 for 24 h compared to untreated cells. While 31 genes were upregulated and 14 genes were downregulated in LoVo cells treated with NS398 for 48 h. IGFBP-5, PAI-2, JUN, REL, BRCA1, and BRCA2 might be the new targets of NS398 in treatment of colorectal cancer.

CONCLUSION: NS398 might exert its anti-metastasis effect on colorectal cancer by affecting several metastasis-associated gene expression.

Keywords: NS398; Colorectal cancer gene expression; Metastasis; cDNA microarray