Promoter hypomethylation of a novel cancer/testis antigen gene CAGE is correlated with its aberrant expression and is seen in premalignant stage of gastric carcinoma

被引:110
作者
Cho, BS
Lee, H
Jeong, S
Bang, YJ
Lee, HJ
Hwang, KS
Kim, HY
Lee, YS
Kang, GH
Jeoung, DI
机构
[1] Kangwon Natl Univ, Coll Nat Sci, Div Life Sci, Chunchon 200701, South Korea
[2] In2Gen Co, Canc Genom Div, Seoul 110799, South Korea
[3] Drug Discovery Inst, R&D Pk, LG Life Sci, Taejon 305380, South Korea
[4] Seoul Natl Univ, Coll Med, Canc Res Inst, Natl Res Lab Canc Epigenet, Seoul 110799, South Korea
[5] Seoul Natl Univ, Coll Med, Dept Pathobiol, Seoul 110744, South Korea
[6] Canc Res Inst, Seoul 110744, South Korea
[7] Hyung Hee Univ, Coll Life Sci, Suwon 449701, South Korea
关键词
CAGE; hypomethylation; transcription; methylation-specific PCR;
D O I
10.1016/S0006-291X(03)01121-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Previously, we reported the identification and characterization of a novel cancer/testis antigen gene, CAGE, that was expressed in various histological types of tumors, but not in normal tissues, with the exception of the testis. To date, molecular mechanisms for the expression of CAGE have never been studied. In our expression analysis, we found that some cancer cell lines did not express CAGE. The expression of CAGE could be restored in these cell lines by treatment with 5'-aza-2'-deoxycytidine, suggesting that the expression of CAGE is mainly suppressed by hypermethylation. Bisulfite sequencing analysis of the 16 CpG sites of the CAGE promoter in various cancer cell lines and tissues revealed a close relationship between the methylation status of the CAGE promoter and the expression of CAGE. The transient transfection experiments displayed that the methylation of CpG sites inhibited the CAGE promoter activity in luciferase reporter assays. The methylation of the CpG sites inhibited the binding of transcription factors, shown by a mobility shift assay. A methylation-specific PCR analysis revealed that hypomethylation of the CAGE promoter was present at frequencies of more than 60% in breast, gastric, and lung cancers, and hepatocellular carcinomas, and at frequencies of less than 40% in prostate, uterine cervical, and laryngeal cancers. Promoter hypomethylation was found in chronic gastritis (19/55, 34.5%) and liver cirrhosis (13/22, 59%), but not in normal prostate, normal colon, or chronic hepatitis. These results suggest that the methylation status of the CpG sites of CAGE determines its expression, that the hypomethylation of CAGE precedes the development of gastric cancer and hepatocellular carcinoma, and that the high frequencies of hypomethylation of CAGE, in various cancers would be valuable as a cancer diagnostic marker. (C) 2003 Elsevier Science (USA). All rights reserved.
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页码:52 / 63
页数:12
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