Hypermethylation of the TSLC1 gene promoter in primary gastric cancers and gastric cancer cell lines

被引:64
作者
Honda, T
Tamura, G
Waki, T
Jin, Z
Sato, K
Motoyama, T
Kawata, S
Kimura, W
Nishizuka, S
Murakami, Y
机构
[1] Yamagata Univ, Sch Med, Dept Pathol, Yamagata 9909585, Japan
[2] Yamagata Univ, Sch Med, Dept Med, Yamagata 9909585, Japan
[3] Yamagata Univ, Sch Med, Dept Surg, Yamagata 9909585, Japan
[4] NCI, Mol Pharmacol Lab, NIH, Bethesda, MD 20892 USA
[5] Natl Canc Ctr, Res Inst, Tumor Suppress & Funct Genomics Project, Chuo Ku, Tokyo 1040045, Japan
来源
JAPANESE JOURNAL OF CANCER RESEARCH | 2002年 / 93卷 / 08期
关键词
gastric cancer; TSLC1; hypermethylation;
D O I
10.1111/j.1349-7006.2002.tb01329.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The TSLC1 (tumor suppressor in lung cancer-1) gene is a novel tumor suppressor gene on chromosomal region 11q23.2, and is frequently inactivated by concordant promoter hypermethylation and loss of heterozygosity (LOH) in non-small cell lung cancer (NSCLC). Because LOH on 11q has also been observed frequently in other human neoplasms including gastric cancer, we investigated the promoter methylation status of TSLC1 in 10 gastric cancer cell lines and 97 primary gastric cancers, as well as the corresponding non-cancerous gastric tissues, by bisulfite-SSCP analysis followed by direct sequencing. Allelic status of the TSLC1 gene was also investigated in these cell lines and primary gastric cancers. The TSLC1 promoter was methylated in two gastric cancer cell lines, KATO-III and ECC10, and in 15 out of 97 (16%) primary gastric cancers. It was not methylated in non-cancerous gastric tissues, suggesting that this hypermethylation is a cancer-specific alteration. KATO-III and ECC10 cells retained two alleles of TSLC1, both of which showed hypermethylation, associated with complete loss of gene expression. Most of the primary gastric cancers with promoter methylation also retained heterozygosity at the TSLC1 locus on 11q23.2. These data indicate that bi-allelic hypermethylation of the TSLC1 promoter and resulting gene silencing occur in a subset of primary gastric cancers.
引用
收藏
页码:857 / 860
页数:4
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