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Gene cataloging and expression profiling in human gastric cancer cells by expressed sequence tags

Authors
Kim, Nam-SoonHahn, YoonsooOh, Jung-HwaLee, a Ju-YeonOh, Kyung-JinKim,Jeong-MinPark, Hong-SeogKim, a SangsooSong, Kyu-Sang SongRho, Seung-MooYoo, Hyang-SookKim,Yong Sung
Issue Date
Jun-2004
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
Keywords
gastric cancer; EST; expression profiling; metastasis
Citation
GENOMICS, v.83, no.6, pp 1024 - 1045
Pages
22
Journal Title
GENOMICS
Volume
83
Number
6
Start Page
1024
End Page
1045
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/57585
DOI
10.1016/j.ygeno.2003.12.002
ISSN
0888-7543
1089-8646
Abstract
To understand the molecular mechanism associated with gastric carcinogenesis, we identified genes expressed in gastric cancer cell lines and tissues. Of 97,609 high-quality ESTs sequenced from 36 cDNA libraries, 92,545 were coalesced into 10,418 human Unigene clusters (Build 151). The gene expression profile was produced by counting the cluster frequencies in each library. Although the profiles of highly expressed genes varied greatly from library to library, those genes related to cell structure formation, heat shock proteins, the glycolysis pathway, and the signaling pathway were highly represented in human gastric cancer cell lines and in primary tumors. Conversely, the genes encoding immunoglobulins, ribosomal proteins, and digestive proteins were down-regulated in gastric cancer cell lines and tissues compared to normal tissues. The transcription levels of some of these genes were confirmed by RT-PCR. We found that genes related to cell adhesion, apoptosis, and cytoskeleton formation were particularly tip-regulated in the gastric cancer cell lines established from malignant ascites compared to those from primary tumors. This comprehensive molecular profiling of human gastric cancer should be useful for elucidating the genetic events associated with human gastric cancer. (C) 2003 Elsevier Inc. All rights reserved.
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Hahn, Yoonsoo
자연과학대학 (생명과학과)
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