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Clinical Cancer Research Vol. 11, 473-482, January 2005
© 2005 American Association for Cancer Research


Human Cancer Biology

Identification of Gastric Cancer–Related Genes Using a cDNA Microarray Containing Novel Expressed Sequence Tags Expressed in Gastric Cancer Cells

Jeong-Min Kim1,5, Ho-Yong Sohn4, Sun Young Yoon1, Jung-Hwa Oh1, Jin Ok Yang1, Joo Heon Kim2, Kyu Sang Song3, Seung-Moo Rho2, Hyan Sook Yoo1, Yong Sung Kim1, Jong-Guk Kim5 and Nam-Soon Kim1

1 Genome Research Center, Korea Research Institute of Bioscience and Biotechnology; 2 Department of Pathology, Eulji University School of Medicine; and 3 Department of Pathology, College of Medicine, Chungnam National University, Daejeon, Korea; 4 Department of Food and Nutrition, Andong National University, Andong, Korea; and 5 Department of Microbiology, College of Natural Sciences, Kyungpook National University, Daegu, Korea

Requests for reprints: Nam-Soon Kim, Laboratory of Human Genomics, Genome Research Center, Korea Research Institute of Bioscience and Biotechnology, P.O. Box 115, Yusong, Daejeon, Korea. Phone: 82-42-879-8112; Fax: 82-42-879-8119; E-mail: nskim37{at}kribb.re.kr.

Purpose: Gastric cancer is one of the most frequently diagnosed malignancies in the world, especially in Korea and Japan. To understand the molecular mechanism associated with gastric carcinogenesis, we attempted to identify novel gastric cancer–related genes using a novel 2K cDNA microarray.

Experimental Design: A 2K cDNA microarray was fabricated from 1,995 novel expressed sequence tags (ESTs) showing no hits or a low homology with ESTs in public databases from our 143,452 ESTs collected from gastric cancer cell lines and tissues. An analysis of the gene expression for human gastric cancer cell lines to a normal cell line was done using this cDNA microarray. Data for the different expressed genes were verified using semiquantitative reverse transcription-PCR, Western blotting, and immunohistochemical staining in the gastric cell lines and tissues.

Results: Forty genes were identified as either up-regulated or down-regulated genes in human gastric cancer cells. Among these, genes such as SKB1, NT5C3, ZNF9, p30, CDC20, and FEN1, were confirmed to be up-regulated genes in nine gastric cell lines and in 25 pairs of tissue samples from patients by semiquantitative reverse transcription-PCR. On the other hand, genes such as MT2A and CXX1 were identified as down-regulated genes. In particular, the SKB1, CDC20, and FEN1 genes were overexpressed in ≥68% of tissues and the MT2A gene was down-expressed in 72% of the tissues. Western blotting and immunohistochemical analyses for CDC20 and SKB1 showed overexpression and localization changes of the corresponding protein in human gastric cancer tissues.

Conclusions: Novel genes that are related to human gastric cancer were identified using cDNA microarray developed in our laboratory. In particular, CDC20 and MT2A represent a potential biomarker of human gastric cancer. These newly identified genes should provide a valuable resource for understanding the molecular mechanism associated with tumorigenesis of gastric carcinogenesis and for the discovery of potential diagnostic markers of gastric cancer.

Key Words: expression profiling • biomarker • carcinogenesis • semiquantitative RT-PCR




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