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鼻咽癌中候选抑癌基因DLC-1的遗传和表观遗传改变

Genetic and epigenetic alterations of DLC-1, a candidate tumor suppressor gene, in nasopharyngeal carcinoma.

作者信息

Peng Dan, Ren Cai-Ping, Yi Hong-Mei, Zhou Liang, Yang Xu-Yu, Li Hui, Yao Kai-Tai

机构信息

Cancer Research Institute, Xiangya School of Medicine, Central South University, Changsha 410078, China.

出版信息

Acta Biochim Biophys Sin (Shanghai). 2006 May;38(5):349-55. doi: 10.1111/j.1745-7270.2006.00164.x.

Abstract

The DLC-1 gene, located at the human chromosome region 8p22, behaves like a tumor suppressor gene and is frequently deleted in diverse tumors. The deletion of 8p22 is not an uncommon event in nasopharyngeal carcinoma (NPC), therefore we explored the expression levels of the DLC-1 gene in NPCs and NPC cell lines by reverse transcription-polymerase chain reaction. The results showed the mRNA level of DLC-1 was downregulated. To identify the mechanism of DLC-1 downregulation in NPC, we investigated the methylation status of the DLC-1 gene using methylation-specific PCR, and found that 79% (31 of 39) of the NPC tissues and two DLC-1 nonexpressing NPC cell lines, 6-10B and 5-8F, were methylated in the DLC-1 CpG island. Microsatellite PCR was also carried out, and loss of heterozygosity was found at four microsatellite sites (D8S552, D8S1754, D8S1790 and D8S549) covering the whole DLC-1 gene with ratios of 33% (4 of 12 informative cases), 18% (2 of 11), 5% (1 of 18), and 25% (3 of 12), respectively. Taken together, our results suggest that DLC-1 might be an NPC-related tumor suppressor gene affected by aberrant promoter methylation and gene deletion.

摘要

DLC-1基因位于人类染色体8p22区域,具有肿瘤抑制基因的功能,在多种肿瘤中常发生缺失。8p22缺失在鼻咽癌(NPC)中并非罕见事件,因此我们通过逆转录-聚合酶链反应探讨了DLC-1基因在NPC组织和NPC细胞系中的表达水平。结果显示DLC-1的mRNA水平下调。为了确定NPC中DLC-1下调的机制,我们使用甲基化特异性PCR研究了DLC-1基因的甲基化状态,发现79%(39例中的31例)的NPC组织以及两个不表达DLC-1的NPC细胞系6-10B和5-8F,其DLC-1 CpG岛发生了甲基化。我们还进行了微卫星PCR,发现在覆盖整个DLC-1基因的四个微卫星位点(D8S552、D8S1754、D8S1790和D8S549)存在杂合性缺失,比例分别为33%(12例信息性病例中的4例)、18%(11例中的2例)、5%(18例中的1例)和25%(12例中的3例)。综上所述,我们的结果表明DLC-1可能是一个与NPC相关的肿瘤抑制基因,受启动子异常甲基化和基因缺失影响。

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