期刊文献+

结肠癌血清microRNA表达谱的检测及临床应用价值 被引量:27

Detection of serum microRNA profile in colon cancer and its clinical application value
下载PDF
导出
摘要 目的找寻潜在的新型的结肠癌血清micro RNA(miRNA)表达谱,探讨其临床应用价值。方法 miRNA微阵列芯片技术检测结肠癌患者和正常人血清中miRNA表达的差异,并对有差异表达的miRNA在60例结肠癌患者血清和60例正常对照组血清中的表达进行实时荧光定量聚合酶链反应(qRT-PCR)验证。结果(1)芯片杂交结果中共有87种miRNAs在结肠癌患者血清和正常人血清标本中有差异表达,其中上调表达有39个,下调表达有48个。(2)qRT-PCR对miRNAs进行验证,其中miR-31、miR-141、miR-224-3p、miR-576-5p和miR-4669这5个miR分子在结肠癌症患者中的表达相对于正常对照组差异具有统计学意义(P<0.05)。(3)miR-31、miR-141、miR-224-3p、miR-576-5p和miR-4669这5个miR分子组成的miR-表达谱诊断结肠癌的效率较高(ROC曲线下面积为0.992)。结论临床检测结肠癌患者miR-31、miR-141、miR-224-3p、miR-576-5p和miR-4669循环分子标志物表达谱有助于诊断结肠癌,有望成为结肠癌患者临床诊疗评估的重要指标。 Objective To explore the potential novel serum microRNA(miRNA)profile in colon cancer and discuss its clinical application value.Methods The difference of serum miRNA expression between colon cancer patients and healthy people was detected by miRNA microarray chip technology.The differential expression of miRNAs in serum of60cases of colon cancer and60normal people were validated by qRT-PCR.Results A total of87miRNAs were differentially expressed in the serum of the colon cancer patients compared to the normal people,among which39miRNAs were upregulated and48miRNAs were down-regulated.miR-31,miR-141,miR-224-3p,miR-576-5p and miR-4669expressions in the colon cancer patients were significantly different from those in the normal control group(P<0.05).MicroRNA profile(including miR-31,miR-141,miR-224-3p,miR-576-5p and miR-4669)has a higher efficiency in diagnosis of colon cancer(area under the ROC curve was0.992).Conclusions Clinical detection of expression profile of circulating molecular markers miR-31,miR-141,miR-224-3p,miR-576-5p and miR-4669in colon cancer patients is useful for the diagnosis of colon cancer.It is expected to be an important index for evaluation of clinical diagnosis and treatment in patients with colon cancer.
作者 王亚南 陈昭华 陈卫昌 Ya-nan Wang;Zhao-hua Chen;Wei-chang Chen(The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu 215006, China;Suzhou Municipal Hospital (Suzhou Hospital Affiliated to Nanjing Medical University), Suzhou, Jiangsu 215002, China)
出处 《中国现代医学杂志》 CAS 2018年第1期37-43,共7页 China Journal of Modern Medicine
基金 苏州市"科教兴卫"青年科技项目(No:KJXW2014017)
关键词 结肠癌 血清microRNA MIRNA colon cancer serum microRNA expression profile
  • 相关文献

参考文献2

二级参考文献33

  • 1Lee R, Feinbaum R, Ambros V. A short history of a short RNA. Cell, 2004, S116(2): s89-s92.
  • 2Ruvkun G, Wightman B, Ha I. The 20 years it took to recognize the importance oftinyRNAs. Ceil, 2004, Sl16(2): s93 -s96.
  • 3Nelson P, Kiriakidou M, Sharma A, et al. The microRNA world: small is mighty. Trends in Biochemical Sciences, 2003, 28(10): 534-540.
  • 4Carrington J C, Ambros V. Role of microRNAs in plant and animal development. Science, 2003, 301(5631): 336-338.
  • 5Barrel D P. MicroRNAs: Genomics, biogenesis, mechanism, and fimction. Cell, 2004,116(2): 281-297.
  • 6Murchison E P, Harmon G J. MiRNAs on the move: miRNA biogenesis and the RNAi machinery. Curt {)pin Cell Biol, 2004, 16(3): 223-229.
  • 7Xie X H, Lu J, Kulbokas E J, et al. Systematic discovery of regulatory motifs in human promoters and 3' UTRs by comparison of several mammals. Nature, 2005, 434(703 1): 338-345.
  • 8Du C S, Liu C, Kang J H, et ol. MicroRNA miR-326 regulates T-H-17 differentiation and is associated with the pathogenesis of multiple sclerosis. Nature Immunology, 2009, 10(12): 1252-1254.
  • 9Zhao Y, Ransom J F, Li A, et 01. Dysregulation of cardiogenesis,cardiac conduction, and cell cycle in mice lacking miRNA-1-2. Cell, 2007, 129(2): 303-317.
  • 10Rosenfeld N, Aharonov R, Meiri E, et al. MicroRNAs accurately identify cancer tissue origin. Nat Biotech, 2008, 26(4): 462-469.

同被引文献266

引证文献27

二级引证文献89

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