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宫颈癌中 TMS1/ASC 和 CASP8 基因的 CpG 岛甲基化。

CpG island methylation of TMS1/ASC and CASP8 genes in cervical cancer.

机构信息

Department of Biotechnology, Panjab University, Chandigrah, India.

出版信息

Eur J Med Res. 2009;14(2):71-5. doi: 10.1186/2047-783x-14-2-71.

Abstract

BACKGROUND

Gene silencing associated with aberrant methylation of promoter region CpG islands is an acquired epigenetic alteration that serves as an alternative to genetic defects in the inactivation of tumor suppressor and other genes in human cancers.

AIMS

This study describes the methylation status of TMS1/ASC and CASP8 genes in cervical cancer. We also examined the prevalence of TMS1/ASC and CASP8 genes methylation in cervical cancer tissue and none--neo plastic samples in an effort to correlate with smoking habit and clinicopathological features.

METHOD

Target DNA was modified by sodium bisulfite, converting all unmethylated, but not methylated, cytosines to uracil, and subsequently amplified by Methylation Specific (MS) PCR with primers specific for methylated versus unmethylated DNA. The PCR product was detected by gel electrophoresis and combined with the clinical records of patients.

RESULTS

The methylation pattern of the TMS1/ASC and CASP8 genes in specimens of cervical cancer and adjacent normal tissues were detected (5/80 (6.2%), 3/80 (3.75%)-2/80 (2.5%), 1/80 (1.2%) respectively). No statistical differences were seen in the extent of differentiation, invasion, pathological type and smoking habit between the methylated and unmethylated tissues (P > 0.05).

CONCLUSION

The present study conclude that the frequency of TMS1/ASC and CASP8 genes methylation in cervical cancer are rare (< 6%), and have no any critical role in development of cervical cancer.

摘要

背景

基因沉默与启动子区域 CpG 岛的异常甲基化有关,是一种获得性表观遗传改变,可替代人类癌症中肿瘤抑制基因和其他基因的遗传缺陷失活。

目的

本研究描述了宫颈癌中 TMS1/ASC 和 CASP8 基因的甲基化状态。我们还检查了宫颈癌组织和非肿瘤样本中 TMS1/ASC 和 CASP8 基因甲基化的发生率,以期与吸烟习惯和临床病理特征相关。

方法

采用亚硫酸氢钠修饰靶 DNA,将所有未甲基化但非甲基化的胞嘧啶转化为尿嘧啶,然后用针对甲基化和未甲基化 DNA 的特异性引物进行甲基化特异性 (MS) PCR 扩增。通过凝胶电泳检测 PCR 产物,并结合患者的临床记录。

结果

检测了宫颈癌和相邻正常组织标本中 TMS1/ASC 和 CASP8 基因的甲基化模式(分别为 5/80(6.2%)、3/80(3.75%)-2/80(2.5%)、1/80(1.2%))。在分化程度、浸润程度、病理类型和吸烟习惯方面,甲基化和非甲基化组织之间没有统计学差异(P > 0.05)。

结论

本研究表明宫颈癌中 TMS1/ASC 和 CASP8 基因甲基化的频率较低(<6%),并且在宫颈癌的发生发展中没有任何关键作用。

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