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谷胱甘肽过氧化物酶 1(GPX1)下调的预后意义及其与人类胃癌中异常启动子甲基化的相关性。

Prognostic significance of glutathione peroxidase 1 (GPX1) down-regulation and correlation with aberrant promoter methylation in human gastric cancer.

机构信息

Department of Pathology, Seoul National University College of Medicine, 28 Yeongeon-dong, Jongno-gu, Seoul 110-799, Republic of Korea.

出版信息

Anticancer Res. 2012 Aug;32(8):3169-75.

Abstract

BACKGROUND

This study aimed at examining the association of gene silencing and promoter methylation of glutathione peroxidase 1 (GPX1) and glutathione peroxidase 3 (GPX3) in gastric cancer cells and determined the clinical significance of GPX1 and GPX3 expression loss in gastric cancer tissue.

MATERIALS AND METHODS

Analysis of mRNA expression was carried out by reverse transcription-polymerase chain reaction (RT-PCR). Methylation of the GPX1 promoter region was analyzed by bisulfite sequencing, and that of the GPX3 promoter region was analyzed by methylation-specific PCR (MSP). Tissue microarray-based immunohistochemistry of GPX1 and GPX3 in 1,163 resected gastric cancer specimens was performed to assess the associations with clinicopathological parameters.

RESULTS

Reduced GPX1 and GPX3 mRNA expression was associated with promoter methylation in gastric cancer cell lines. A correlation between DNA promoter methylation and loss of GPX1 expression was noted in 16 gastric cancer tissue samples (p=0.005). Loss of GPX1 and GPX3 proteins was found in 24.4% and 30.8% of gastric cancer tissues. Loss of GPX1 expression was significantly associated with advanced gastric cancer (p=0.039) and lymphatic invasion (p=0.010); loss of GPX3 expression was associated with advanced gastric cancer (p<0.001) and lymph node metastasis (p<0.001). Kaplan-Meier analysis showed that low expression of GPX1 was associated with poor cancer-specific survival (p=0.010).

CONCLUSION

Data from this study implicate aberrant hypermethylation of promoter regions of GPX1 and GPX3 as a mechanism for down-regulation of GPX1 and GPX3 mRNA expression in gastric cancer cells. Loss of GPX1 expression was associated with aggressiveness and poor survival in patients with gastric cancer.

摘要

背景

本研究旨在探讨谷胱甘肽过氧化物酶 1 (GPX1) 和谷胱甘肽过氧化物酶 3 (GPX3) 基因沉默和启动子甲基化在胃癌细胞中的相关性,并确定胃癌组织中 GPX1 和 GPX3 表达缺失的临床意义。

材料和方法

采用逆转录-聚合酶链反应 (RT-PCR) 分析 mRNA 表达。通过亚硫酸氢盐测序分析 GPX1 启动子区域的甲基化,通过甲基化特异性 PCR (MSP) 分析 GPX3 启动子区域的甲基化。对 1163 例胃癌切除标本进行基于组织微阵列的 GPX1 和 GPX3 免疫组织化学分析,以评估与临床病理参数的相关性。

结果

胃癌细胞系中 GPX1 和 GPX3 mRNA 表达降低与启动子甲基化有关。在 16 例胃癌组织样本中观察到 DNA 启动子甲基化与 GPX1 表达缺失之间存在相关性 (p=0.005)。在 24.4%和 30.8%的胃癌组织中发现 GPX1 和 GPX3 蛋白缺失。GPX1 表达缺失与胃癌晚期显著相关 (p=0.039) 和淋巴浸润相关 (p=0.010);GPX3 表达缺失与胃癌晚期 (p<0.001) 和淋巴结转移相关 (p<0.001)。Kaplan-Meier 分析显示,GPX1 低表达与癌症特异性生存不良相关 (p=0.010)。

结论

本研究数据表明,GPX1 和 GPX3 启动子区域的异常高甲基化是胃癌细胞中 GPX1 和 GPX3 mRNA 表达下调的机制。GPX1 表达缺失与胃癌患者的侵袭性和不良预后相关。

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