期刊文献+

MS-HRM在遗传性非息肉性大肠癌筛查中的应用 被引量:1

Methylation-specific high-resolution melting analysis for screening hereditary nonpolyposis colorectal cancer
下载PDF
导出
摘要 目的探讨甲基化敏感性高分辨率熔解曲线分析(MS-HRM)在遗传性非息肉性大肠癌(HNPCC)筛查中的应用价值。方法采用实时荧光定量PCR技术检测miR-195在41例散发性大肠癌(SCRC)和9例HNPCC患者癌组织及对应癌旁正常组织(距离癌组织>5 cm)中的表达水平,随后使用MS-HRM检测miR-195启动子区域CpG岛甲基化情况。结果 miR-195在HNPCC癌组织中的表达量为1.20±1.48,甲基化比例为55.56%(5/9);miR-195在SCRC组织中的表达量为0.76±1.06,甲基化比例为58.54%(24/41),差异无统计学意义(P>0.05);miR-195在肠癌组织及癌旁正常组织中的平均表达水平分别为0.837±1.145和2.236±2.468,差异具有统计学意义(P<0.05)。结论 miR-195在SCRC和HNPCC癌组织中的表达有无差异尚待进一步研究。miR-195可能有助于抑制肠癌发展,并且因其甲基化而参于大肠癌的发病机制。 Objective To investigate the application value of methylation-specific high-resolution melting analysis (MS-HRM) for screening hereditary non-polyposis colorectal cancer (HNPCC).Methods The expression of miR-195 in 41cases of SCRC and 9 cases of HNPCC and adjacent non-tumor mucosa tissues (5 cm away from the cancer tissue)were detected by Real-time PCR.Then MS-HRM was used to detect the methylation of miR-195 promoter regions CpG island.Results The expression of miR-195 in HNPCC and SCRC cancer tissue were 1.20 ± 1.48,0.76 ± 1.06,respectively.MS-HRM showed that the methylation rates of miR-195 in HNPCC cancer tissue and SCRC cancer tiscues were 55.56% (5/9),58.54% (24/41),respectively.There was no statistically significant difference (P > 0.05).However,the average expression of miR-195 in human colon carcinoma and adjacent normal mucosa were 0.837 ± 1.145 and 2.236 ± 2.468,there was significant difference (P < 0.05).Conclusion The differential expression of miR-195 between HNPCC and SCRC needs further research.miR-19 may inhibit the development of colorectal cancer,and participate in the pathogenesis of colorectal cancer for methylation.
出处 《胃肠病学和肝病学杂志》 CAS 2014年第9期1047-1049,共3页 Chinese Journal of Gastroenterology and Hepatology
基金 广东省自然科学基金资助项目(No:S2011010005494) 广东省惠州市科技计划项目(No:2011Y091)
关键词 遗传性非息肉性大肠癌 甲基化敏感性高分辨率熔解曲线分析 miR-195 Hereditary non-polyposis colorectal cancer Methylation-specific high-resolution melting analysis miR-195
  • 相关文献

参考文献10

  • 1Yu Z,Zhi J,Peng X,et al.Clinical signifcance of HSP27 expression in colorectal cancer[J].Mol Med Rep,2010,3(6):953-958.
  • 2Lin AY,Kouzminova NB,Pollack J,et al.Prognostic role of microRNA-34a expression in colorectal cancer[J].J Clin Oncol,2014,32(3 Suppl):472.
  • 3Hur K,Toiyama Y,Takahashi M,et al.MicroRNA-200c modulates epithelial-to-mesenchymal transition (EMT) in human colorectal cancer metastasis[J].Gut,2013,62(9):1315-1326.
  • 4Stintzing S,Lenz HJ.MicroRNA-21 in Colorectal Cancer:" Just another brick in the wall"?[J].J Natl Cancer Inst,2013,105(12):840-841.
  • 5Wang X,Wang J,Ma H,et al.Downregulation of miR-195 correlates with lymph node metastasis and poor prognosis in colorectal cancer[J].Med Oncol,2012,29(2):919-927.
  • 6Vasen HF,Blanco I,Aktan-Collan K,et al.Revised guidelines for the clinical management of Lynch syndrome (HNPCC):recommendations by a group of European experts[J].Gut,2013,62 (6):812-823.
  • 7Eckardt NA.The plant cell reviews aspects of microRNA and PhasiRNA regulatory function[J].Plant Cell,2013,25(7):2382.
  • 8Gregersen LH,Jacobsen A,Frankel LB,et al.MicroRNA-143 downregulates Hexokinase 2 in colon cancer cells[J].BMC Cancer,2012,12:232.
  • 9Wojdacz TK,Moller TH,Thestrup BB,et al.Limitations and advantages of MS-HRM and bisulfite sequencing for single locus methylation studies[J].Expert Rev Mol Diagn,2010,10(5):575-580.
  • 10Menigatti M,Staiano T,Manser CN,et al.Epigenetic silencing of monoallelically methylated miRNA loci in precancerous colorectal lesions[J].Oncogenesis,2013,2:e56.

同被引文献18

引证文献1

二级引证文献5

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