Nojima M, Suzuki H, Toyota M, Watanabe Y, Maruyama R, Sasaki S, Sasaki Y, Mita H, Nishikawa N, Yamaguchi K, Hirata K, Itoh F, Tokino T, Mori M, Imai K, Shinomura Y
First Department of Internal Medicine, Sapporo Medical University, Sapporo, Japan.
Oncogene. 2007 Jul 12;26(32):4699-713. doi: 10.1038/sj.onc.1210259. Epub 2007 Feb 5.
Activation of Wnt signaling has been implicated in gastric tumorigenesis, although mutations in APC (adenomatous polyposis coli), CTNNB1 (beta-catenin) and AXIN are seen much less frequently in gastric cancer (GC) than in colorectal cancer. In the present study, we investigated the relationship between activation of Wnt signaling and changes in the expression of secreted frizzled-related protein (SFRP) family genes in GC. We frequently observed nuclear beta-catenin accumulation (13/15; 87%) and detected the active form of beta-catenin in most (12/16; 75%) GC cell lines. CpG methylation-dependent silencing of SFRP1, SFRP2 and SFRP5 was frequently seen among GC cell lines (SFRP1, 16/16, 100%; SFRP2, 16/16, 100%; SFRP5, 13/16, 81%) and primary GC specimens (SFRP1, 42/46, 91%; SFRP2, 44/46, 96%; SFRP5, 30/46, 65%), and treatment with the DNA methyltransferase inhibitor 5-aza-2'-deoxycytidine rapidly restored SFRP expression. Ectopic expression of SFRPs downregulated T-cell factor/lymphocyte enhancer factor transcriptional activity, suppressed cell growth and induced apoptosis in GC cells. Analysis of global expression revealed that overexpression of SFRP2 repressed Wnt target genes and induced changes in the expression of numerous genes related to proliferation, growth and apoptosis in GC cells. It thus appears that aberrant SFRP methylation is one of the major mechanisms by which Wnt signaling is activated in GC.
Wnt信号通路的激活与胃癌发生有关,尽管与结直肠癌相比,胃癌(GC)中腺瘤性息肉病基因(APC)、β-连环蛋白(CTNNB1)和轴抑制蛋白(AXIN)的突变频率要低得多。在本研究中,我们调查了GC中Wnt信号通路激活与分泌型卷曲相关蛋白(SFRP)家族基因表达变化之间的关系。我们经常观察到β-连环蛋白在细胞核内积聚(13/15;87%),并在大多数(12/16;75%)GC细胞系中检测到β-连环蛋白的活性形式。在GC细胞系(SFRP1, 16/16, 100%;SFRP2, 16/16, 100%;SFRP5, 13/16, 81%)和原发性GC标本(SFRP1, 42/46, 91%;SFRP2, 44/46, 96%;SFRP5, 30/46, 65%)中经常可见SFRP1、SFRP2和SFRP5因CpG甲基化而沉默,用DNA甲基转移酶抑制剂5-氮杂-2'-脱氧胞苷处理可迅速恢复SFRP表达。SFRP的异位表达下调了T细胞因子/淋巴细胞增强因子的转录活性,抑制了GC细胞的生长并诱导其凋亡。整体表达分析显示,SFRP2的过表达抑制了Wnt靶基因,并诱导了GC细胞中许多与增殖、生长和凋亡相关基因的表达变化。因此,SFRP异常甲基化似乎是GC中激活Wnt信号通路的主要机制之一。