Song Yu, Zuo Yun
Department of Oncology, Zhangjiagang First People's Hospital, Suzhou, Jiangsu 215600, P.R. China.
Oncol Lett. 2014 Nov;8(5):2340-2344. doi: 10.3892/ol.2014.2518. Epub 2014 Sep 10.
The present study aimed to observe the methylation status of the CpG islands at the human hedgehog interacting protein (HHIP) gene in gastric cancer tissues, peritumoral tissues and the AGS cell line, to analyze the association between the methylation status of the CpG islands and the tumorigenesis of gastric cancer. The HHIP mRNA expression in 60 human gastric carcinnoma tissues, peritumoral tissues and the gastric carcinoma AGS cell line were detected by reverse transcription polymerase chain reaction (RT-PCR). The HHIP methylation status of the promoter region in the gastric carcinnoma tissues and peritumoral tissues was detected by methylation-specific PCR (MSP). Prior to and following treatment with methyl transferase inhibitor 5-aza-2'-deoxycitydine (5-aza-dc), the HHIP mRNA expression level, the methylation status of the promoter region and the methylation site loci on the CpG islands in the AGS cells were detected by RT-PCR, MSP and bisulfite sequencing PCR (BSP), respectively. The correlation between the methylation status of the CpG islands at the HHIP promoter region and the HHIP mRNA expression level were analyzed. It was found that the expression level of the HHIP mRNA in the gastric carcinoma tissues was significantly lower than that in the adjacent tissues (0.82±0.38 vs. 1.60±0.26, respectively; P<0.001). No significant correlations were observed between the expression of HHIP mRNA and age, gender, tumor-node-metastasis stage, differentiation degree and presence of lymph node metastasis (P>0.05). The degree of methylation of the HHIP gene promotor in the peritumoral tissues (17.7±3.59%) was significantly lower than that in the gastric cancer tissues (62.9±6.14%) and in the AGS cells (99.7±0.67%) (P<0.05). Compared with prior to 5-aza-dc intervention, the HHIP mRNA expression level in the AGS cells was significantly increased subsequent to intervention (0.21±0.12 vs. 4.68±0.22; P<0.01), while the degree of methylation in the AGS cells was significantly decreased (90.2±0.67 vs. 10.1±0.21%; P<0.01), and the methylation sites in CpG islands were significantly reduced. The degree of HHIP methylation showed a negative correlation with the level of mRNA expression (r=-0.693; P<0.01). It can be hypothesized that a high degree of methylation of the HHIP gene promoter CpG islands in gastric cancer tissues and cells causes a decrease in HHIP mRNA expression, which may be involved in the carcinogenesis of gastric cancer.
本研究旨在观察人刺猬因子相互作用蛋白(HHIP)基因在胃癌组织、癌旁组织及AGS细胞系中CpG岛的甲基化状态,分析CpG岛甲基化状态与胃癌发生的关系。采用逆转录聚合酶链反应(RT-PCR)检测60例人胃癌组织、癌旁组织及胃癌AGS细胞系中HHIP mRNA的表达。采用甲基化特异性PCR(MSP)检测胃癌组织和癌旁组织中启动子区域的HHIP甲基化状态。在甲基转移酶抑制剂5-氮杂-2'-脱氧胞苷(5-aza-dc)处理前后,分别采用RT-PCR、MSP和亚硫酸氢盐测序PCR(BSP)检测AGS细胞中HHIP mRNA表达水平、启动子区域甲基化状态及CpG岛上的甲基化位点。分析HHIP启动子区域CpG岛甲基化状态与HHIP mRNA表达水平的相关性。结果发现,胃癌组织中HHIP mRNA表达水平显著低于癌旁组织(分别为0.82±0.38 vs. 1.60±0.26;P<0.001)。未观察到HHIP mRNA表达与年龄、性别、肿瘤-淋巴结-转移分期、分化程度及淋巴结转移之间存在显著相关性(P>0.05)。癌旁组织中HHIP基因启动子的甲基化程度(17.7±3.59%)显著低于胃癌组织(62.9±6.