建立鼻咽癌中泛素羧基末端水解酶1基因启动子甲基化检测方案

T. Hue, Huynh Thi Mong Tuyen, N. Truong, Dao Duy Tin, T. Khoa, L. Thuy, L. D. Thuan
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引用次数: 0

摘要

背景:泛素羧基末端水解酶1 (Ubiquitin Carboxyl Terminal Hydrolase 1, UCHL1)基因启动子甲基化已被报道为鼻咽肿瘤发生的病因。目的:本研究旨在建立一种检测越南人群鼻咽癌(NPC)中UCHL1基因启动子甲基化的方案。材料与方法:收集当地医院鼻咽癌活检组织10份,非癌性拭子10份。建立了氯仿/苯酚法和巢式msp法检测目标基因的甲基化。结果:分离得到的DNA在260nm和280nm处的吸光度测定方法证实其纯度和浓度较高。此外,在琼脂糖凝胶中,对甲基化或非甲基化的巢状msp产物进行了分析和可视化,条带分别为169bps和210bps。通过测序证实,这两组引物可以区分UCHL1基因启动子的甲基化和非甲基化状态。结论:我们的数据表明,目前的方案可以成功地识别UCHL1基因启动子的甲基化和/或非甲基化状态。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Establishing protocol for detecting methylation of Ubiquitin carboxyl terminal hydrolase 1 gene’s promoter in nasopharyngeal carcinoma
Background: The methylation of Ubiquitin Carboxyl Terminal Hydrolase 1 (UCHL1) gene’s promoter has been reported as the etiological factor of nasopharyngeal tumorigenesis. Purpose: This study is designed to establish a protocol for detecting methylation of UCHL1 gene’s promoter in nasopharyngeal carcinoma (NPC) in a Vietnamese population. Materials and methods: 10 samples of NPC biopsy tissues and 10 samples of non-cancerous swabs were collected from the local hospital. Chloroform/Phenol method and Nested-MSP assays were established to detect methylation of a target gene. Results: The isolated DNA reached purity and high concentration which were confirmed by the method of absorbance measurement at 260nm and 280nm. Additionally, the Nested-MSP products of methylation or unmethylation were analyzed and visualized in the agarose gel with the band of 169bps and 210bps, respectively. By sequencing, it was confirmed that the two sets of primer could distinguish the status of methylation and unmethylation of UCHL1 gene’s promoter. Conclusion: Our data suggested that the current protocol could successfully identify the status of methylation and/or unmethylation of UCHL1 gene’s promoter.
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