摘要
目的研究喉癌肿瘤组织中微小RNA-129-2基因(MiR-129-2)的甲基化程度及其与患者临床分级和癌组织病理分化程度的关系。方法应用Methyl-ProfilerTM DNA甲基化PCR系统对12例喉癌肿瘤组织和6例癌旁组织进行甲基化分析。结果喉癌组织中MiR-129-2高甲基化率为66.7%(8/12),癌旁组织中MiR-129-2高甲基化率为0(0/6),两组比较差异有统计学意义(P<0.05)。喉癌患者临床分级与MiR-129-2高甲基化率差异无统计学意义(P>0.0 5)。病理分化程度与MiR-1 2 9-2高甲基化率差异无统计学意义(P>0.0 5)。结论 MiR-1 2 9-2基因在喉癌组织中甲基化水平升高,MiR-1 2 9-2高甲基化水平可能与喉癌发生的病理机制有关。
Objective To assess the methylation level of MicroRNA- 129-2 (MiR- 129-2 ) in laryngeal cancer. Methods We applied Methyl-ProfilerTM DNA PCR Array System ( SABiosciences Company ) to analysis of 12 laryngeal cancer and 6 paracancer tissues. Results Hypermethylation was detected in 66. 7 % of the cancer tissue ( 8 / 12 ) and none in paracancer tissue ( 0 / 6 ) ( P 〈 0. 05 ) ; the difference was significant. Among the clinical cancer tissue of each clinical stage , there was no significant difference of MiR-129-2 hypermethylation rate ( P 〉 0. 05 ) . There was no significant difference of MiR- 129 - 2 hypermethylation rate between two pathologic grades ( P 〉 0.05 ). Conclusion The methylation level of MiR- 129 - 2 is higher in laryngeal cancer tissue than in paracancer tissue, indicating that it may play a role in laryngeal cancer. The methylation level of MiR-129-2 may not be related with the clinical stage of laryngeal cancer. The methylation level of MiR: 129-2 may not be related with the pathologic grade of laryngeal cancer.
出处
《中国耳鼻咽喉颅底外科杂志》
CAS
2011年第6期406-411,418,共7页
Chinese Journal of Otorhinolaryngology-skull Base Surgery
基金
<鼻咽癌纯瘤组织中分子标记物筛选及其临床应用研究>(北京市首都发展基金重点项目
编号No.SF07-11-01)项目资助
关键词
喉肿瘤
癌
微小RNA
甲基化
Laryngeal neoplasms, cancer
MicroRNA
Methylation