Okochi-Takada Eriko, Nakazawa Kazuyuki, Wakabayashi Mika, Mori Akiko, Ichimura Shizue, Yasugi Toshiharu, Ushijima Toshikazu
Carcinogenesis Division, National Cancer Center Research Institute, Tokyo, Japan.
Int J Cancer. 2006 Sep 15;119(6):1338-44. doi: 10.1002/ijc.22025.
Aberrant DNA methylation is associated with many types of human cancers. To identify genes silenced in human colorectal cancers, we performed a microarray analysis for genes whose expression was induced by treatment of HCT116 human colon cancer cells with a demethylating agent, 5-aza-2'-deoxycitidine (5-aza-dC). Seven known genes were identified as being upregulated (> or =8-fold) and expressed at more than twice as high as the average level. Among these was the UCHL1 gene (also known as PGP9.5), which is involved in regulation of cellular ubiquitin levels. A dense CpG island in its promoter region was completely methylated in HCT116 cells, and no mRNA was detected. 5-Aza-dC treatment of HCT116 cells induced dose-dependent demethylation of the CpG island, and restored UCHL1 mRNA and protein expression. UCHL1 silencing was observed in 11 of 12 human colorectal cancer cell lines, and its methylation was detected in 8 of 17 primary colorectal cancers. Further, UCHL1 silencing was observed in 6 of 13 ovarian cancer cell lines, and its methylation was detected in 1 of 17 primary ovarian cancers. These results showed that UCHL1 is inactivated in human colorectal and ovarian cancers by its promoter methylation, and suggest that disturbance of cellular ubiquitin levels is present.
异常的DNA甲基化与多种人类癌症相关。为了鉴定在人类结直肠癌中沉默的基因,我们对用去甲基化剂5-氮杂-2'-脱氧胞苷(5-aza-dC)处理HCT116人结肠癌细胞后诱导表达的基因进行了微阵列分析。鉴定出7个已知基因上调(≥8倍)且表达水平高于平均水平两倍以上。其中包括UCHL1基因(也称为PGP9.5),它参与细胞泛素水平的调节。其启动子区域的一个密集CpG岛在HCT116细胞中完全甲基化,未检测到mRNA。用5-aza-dC处理HCT116细胞可诱导CpG岛的剂量依赖性去甲基化,并恢复UCHL1 mRNA和蛋白表达。在12个人类结肠癌细胞系中的11个中观察到UCHL1沉默,在17个原发性结直肠癌中的8个中检测到其甲基化。此外,在13个卵巢癌细胞系中的6个中观察到UCHL1沉默,在17个原发性卵巢癌中的1个中检测到其甲基化。这些结果表明,UCHL1在人类结直肠癌和卵巢癌中因其启动子甲基化而失活,并提示存在细胞泛素水平的紊乱。