期刊文献+

喉癌组织中微小RNA-129-2基因甲基化程度的研究 被引量:1

Methylation of MicroRNA-129-2 in Laryngeal Cancer
下载PDF
导出
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 微小RNA 甲基化 Laryngeal neoplasms, cancer MicroRNA Methylation
  • 相关文献

参考文献17

  • 1Chen CZ,MicroRNAs as oncogenes and tumor suppressors[J].New England Journal of Medicine,2005,353(17):1768-1771.
  • 2Huang YW,Liu JC,Deatherage DE,et al.Epigenetic Re-pression of microRNA-129-2Leads to Overexpression ofSOX 4Oncogene in Endometrial Cancer[J].Cancer Res,2009,69(23):9038-9046.
  • 3Dyrskjot L,Ostenfeld MS,Bramsen JB,et al.GenomicProfiling of MicroRNAs in Bladder Cancer:miR-129Is As-sociated with Poor Outcome and Promotes Cell Death In vitro[J].Cancer Res,2009,69(11):4851-4860.
  • 4Shen R,Pan S,Qi S,et al.Epigenetic repression of mi-croRNA-129-2leads to overexpression of SOX 4in gastriccancer[J].Biochemical and Biophysical Research Communi-cations,2010,394(4):1047-1052.
  • 5Díaz Prado S,Medina Villaamil V,Aparicio Gallego G,etal.Expression of Wnt gene family and frizzled receptors inhead and neck squamous cell carcinomas[J].Virchows Ar-chiv,2009,455(1):67-75.
  • 6Goldberg AD,Allis CD,Bernstein E,Epigenetics:a land-scape takes shape[J].Cell,2007,128(4):635-638.
  • 7Jones PA,Baylin SB,The epigenomics of cancer[J].Cell,2007,128(4):683-692.
  • 8Baylin SB,Ohm JE,Epigenetic gene silencing in cancer-amechanism for early oncogenic pathway addiction[J].NatureReviews,2006,Cancer,6(2):107-116.
  • 9Sinner D,Kordich JJ,Spence JR,et al.Sox17and Sox4Differentially Regulate{beta}-Catenin/T-Cell Factor Activi-ty and Proliferation of Colon Carcinoma Cells[J].Mol CellBiol,2007,27(22):7802-7815.
  • 10Scharer CD,McCabe CD,Ali-Seyed M,et al.Genome-Wide Promoter Analysis of the SOX 4Transcriptional Networkin Prostate Cancer Cells[J].Cancer Res,2009,69(2):709-717.

同被引文献2

引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部