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胃癌中启动子甲基化的定量分析。

Quantitative analysis of promoter methylation in gastric carcinoma.

作者信息

Kim Ho Goon, Ryu Seong Yeob, Lee Kyung Hwa, Lee Jae Hyuk, Kim Dong Yi

机构信息

Division of Gastroenterologic Surgery, Department of Surgery, Chonnam National University Medical School, Gwangju, Korea.

Department of Pathology, Chonnam National University Medical School, Gwangju, Korea.

出版信息

Ann Surg Treat Res. 2018 Aug;95(2):55-63. doi: 10.4174/astr.2018.95.2.55. Epub 2018 Jul 30.

DOI:10.4174/astr.2018.95.2.55
PMID:30079321
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6073046/
Abstract

PURPOSE

To determine the occurrence of methylation in gastric carcinoma (GC), the status and level of CpG methylation in the promoter region of () were analyzed in early and advanced GCs, as well as in normal gastric tissues.

METHODS

The extent of promoter methylation of the gene was assessed quantitatively using pyrosequencing in 60 early and 60 advanced GCs samples harvested upon gastrectomy, and 40 normal gastric mucosa samples from patients with benign gastric diseases as controls.

RESULTS

The methylation frequency for the gene was significantly higher in early than in advanced GCs (40.0% . 20.0%, P < 0.05). A significant difference was found in methylation between GCs and normal gastric tissues (30.0% . 10.0%, by PS; P < 0.05). gene methylation was significantly associated with the depth of invasion (P = 0.003), lymph node metastasis (P = 0.009), distant metastasis (P = 0.036), and TNM staging (P = 0.007). The overall survival of patients with methylation was significantly lower than that of patients without methylation (P = 0.005).

CONCLUSION

These results demonstrated that promoter methylation was significantly higher in tumor tissues, and was an early event for GC, thus, gene methylation may be important in the initial development of gastric carcinogenesis. Thus, GCs with methylation in may not be good candidates for treatment with inhibitors. Furthermore, methylation could be a significant prognostic factor predicting a favorable effect on GC patient outcome when downregulated.

摘要

目的

为了确定胃癌(GC)中甲基化的发生情况,分析了早期和进展期GC以及正常胃组织中()启动子区域的CpG甲基化状态和水平。

方法

采用焦磷酸测序法定量评估60例早期和60例进展期GC切除标本以及40例来自良性胃部疾病患者的正常胃黏膜标本(作为对照)中基因启动子甲基化程度。

结果

基因的甲基化频率在早期GC中显著高于进展期GC(40.0%对20.0%,P<0.05)。在GC与正常胃组织之间发现甲基化存在显著差异(通过PS检测,30.0%对10.0%;P<0.05)。基因甲基化与浸润深度(P = 0.003)、淋巴结转移(P = 0.009)、远处转移(P = 0.036)及TNM分期(P = 0.007)显著相关。甲基化患者的总生存期显著低于未甲基化患者(P = 0.005)。

结论

这些结果表明,肿瘤组织中启动子甲基化显著更高,且是GC的早期事件,因此,基因甲基化可能在胃癌发生的初始发展中起重要作用。因此,甲基化的GC可能不是抑制剂治疗的良好候选对象。此外,甲基化可能是一个重要的预后因素,当基因甲基化下调时对GC患者预后有良好影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac03/6073046/51af7a8baf09/astr-95-55-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac03/6073046/804845668462/astr-95-55-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac03/6073046/24dfcc14c1a7/astr-95-55-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac03/6073046/51af7a8baf09/astr-95-55-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac03/6073046/804845668462/astr-95-55-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac03/6073046/24dfcc14c1a7/astr-95-55-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac03/6073046/51af7a8baf09/astr-95-55-g003.jpg

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胃癌发生多步骤进程中异常CpG岛甲基化图谱
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Int J Oncol. 2003 May;22(5):1025-31.
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