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Reduced expression of the insulin‐induced protein 1 and p41 Arp2/3 complex genes in human gastric cancers

DNA甲基化 甲基化 CpG站点 分子生物学 基因 发起人 外显子 生物 DNA 癌症 癌症研究 基因表达 遗传学
作者
Atsushi Kaneda,Michio Kaminishi,Yukihiro Nakanishi,Takashi Sügimura,Toshikazu Ushijima
出处
期刊:International Journal of Cancer [Wiley]
卷期号:100 (1): 57-62 被引量:45
标识
DOI:10.1002/ijc.10464
摘要

Abstract Aberrantly methylated DNA fragments in a human gastric cancer were searched for by a genome‐scanning method, methylation‐sensitive‐representational difference analysis (MS‐RDA). Six DNA fragments flanked by CpG islands (CGIs) and hypermethylated in the cancer were isolated. Four of the 6 fragments possessed genes in their vicinities. Quantitative RT‐PCR analysis of the 4 genes showed reduced expression of 2 genes in cancers: Insulin‐induced protein 1 (INSIG1/CL‐6) and p41 Arp2/3 complex (p41‐Arc). As for INSIG1 , a DNA fragment was derived from the edge of a CGI in the promoter region. The edge was methylated in 11 of 22 primary gastric cancers, whereas the center was not methylated in any cancer. INSIG1 expression was markedly reduced in 19 cancers, including the 11 cancers with the methylation. By 5‐aza‐2′‐deoxycytidine treatment of 5 cell lines with the methylation of the edge, partial restoration of INSIG1 expression was detected only in 2 of them. These data indicated that, although the reduced INSIG1 expression in cancers was associated with the methylation at the edge of the CGI in the promoter region, the methylation was likely to be a secondary change. As for p41‐Arc, a DNA fragment was derived from a CGI overlapping exon 8, and its methylation did not correlate with its expression. However, methylation of a CGI in the promoter region with a marked reduction of its expression was observed in 1 of the 22 primary cancers. INSIG1 and p41‐Arc are known to be involved in cellular differentiation and morphology, respectively, and it was suggested that their reduced expressions might be involved in gastric cancer development or progression. © 2002 Wiley‐Liss, Inc.
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