摘要
目的探讨H19等位基因在宫颈癌中特异性表达的模式,H19基因的基因组印记缺失与宫颈癌两者之间的关系。方法结合PCR和限制性片段长度多态性分析(RFLP)技术以及DNA甲基化检测技术分析我院收集的宫颈癌标本H19等位基因进行杂合子筛选,并进一步研究基因组印记缺失与宫颈癌两者之间的关系。结果在36例宫颈癌中筛选出16例杂合子现象的标本,在这16例杂合子标本中,有7例发生了基因组印记缺失;H19基因发生基因组缺失现象与其启动子区域的高度去甲基化正相关。结论H19基因的基因组印记缺失可能和宫颈癌的发生有着高度的相关性。
Objective To investigate status of H19 gene imprinting and methylation in H19's CBS6 region in uterine cervical cancer.Methods With PCR-RFLP and bisulfite treatment of genomic DNA,it was analyzed of H19 gene specific-ex-pressing panel and methylation at CpG sites in H19's CBS6 region in 36 uterine cervical cancer samples in our hospital.Results It was identified that LOI of H19 gene in 7 uterine cervical cancer samples among 36 uterine cervical cancer samples,and that LOI of H19 gene could be linked to hypomethylation but not hypermethylation.Conclusion The frequent LOI of H19 gene might play an important role in the development of uterine cervical cancer.
出处
《中国现代医药杂志》
2008年第11期31-33,共3页
Modern Medicine Journal of China