期刊文献+

微小RNA在结肠癌组织中的表达及其临床意义 被引量:4

Down-regulative expression of microRNAs cluster in human colon tumorigenesis
原文传递
导出
摘要 目的研究结肠癌组织与对应正常结肠组织微小RNA(miRNA)的表达特征及其在结肠癌诊断中的意义。方法取天津市肿瘤医院2004至2007年手术切除的15例晚期结肠癌组织标本及其癌旁正常组织标本。通过定量PCR(qRT-PCR)法检测6例结肠癌及其癌旁正常结肠组织的手术标本中200种miRNA的表达情况,应用问题分析(PAM)法对其他9例结肠癌组织及其癌旁正常结肠组织进行定性判断(癌和非癌)。结果6例结肠癌及其癌旁正常结肠组织中存在132种miRNA,其中47种miRNA在结肠癌发生过程中表达量显著下降(〈0.66)。应用PAM法对9对结肠癌组织/远端正常结肠组织进行定性判断的结果与病理切片诊断结果基本一致(吻合度准确率11/12)。结论miRNA与结肠癌的发生发展有密切的联系,有可能成为一个有效的肿瘤标志物以进行结肠癌的早期预测和诊断。 Objective To investigate the features of expression of miRNAs in colon cancer and corresponding normal tissues and the significance thereof in the diagnosis of colon cancer. Methods Fifteen pair samples of colon cancer and matched adjacent normal tissue were collected during operation. A high-throughput real-time quantitative RT-PCR method designed to detect mature miRNA sequences was adapted to screen miRNA expression patterns in 6 pairs of matched colon cancer and normal adjacent tissue samples. Northern blotting was conducted to verify the accuracy of the real-time qRT-PCR assay. Moreover, a thermostable reverse transcriptase based real-time qRT-PCR assay designed to quantify the miRNA precursors was performed. Problem analysis method was used to quantitatively determine the characteristics (cancer or non-cancer) of the other 9 pair samples. Results Among the more than 200 miRNAs exam-ined, 132 were found to be expressed in both the colon cancer and normal adjacent tissue samples. Compared with normal tissue, 47 kinds of miRNA in cancer were down-regnlated (less than 0.66 ). The results of qualitative determination on the 9 samples of cancer tissue/normal tissue were con-sistent with the results of pathological examination. Conclusion Closely linked with the pathogenesis and development of colon cancer, miRNA may be a promising diagnostic biomarker in diagnosis of colon cancer.
出处 《中华医学杂志》 CAS CSCD 北大核心 2008年第24期1683-1686,共4页 National Medical Journal of China
基金 国家自然科学基金资助项目(30772484)
关键词 微RNAS 结肠肿瘤 聚合酶链反应 肿瘤标记 生物学 MiroRNAs Colonic neoplasms Polymerase chain reaction Tumor markers,biological
  • 相关文献

参考文献10

  • 1He L, Hannon GJ. Micromas : small RNAs with a big role in gene regulation. Nat Rev Gene, 2004, 5:522-531.
  • 2Esquela-Kerscher A, Slack FJ. Oncomirs-microRNAs with a role in cancer. Nat Rev Cancer, 2006, 6:259-269.
  • 3Calin GA, Croce CM. MicroRNA signatures in human cancers. Nat Rev Cancer, 2006, 6:857-866.
  • 4Chen CF, Ridzon DA, Broomer A J, et al. Real-time quantification of microRNAs by stem-loop RT-PCR. Nucleic Acids Res, 2005, 33 :e179.
  • 5Schmittgen TD, Jiang J, Liu Q, et al. A high-throughput method to monitor the expression of microRNA precursors. Nucleic Acids Res, 2004, 32 :e43.
  • 6Jemal A, Siegel R, Ward E. Cancer statistics 2007. CA Cancer J Clin, 2007, 57:43- 66.
  • 7王振军,黄莚庭.应进一步加强我国结肠癌的基础研究[J].中华医学杂志,2004,84(9):705-707. 被引量:22
  • 8Tibshirani R, Hastie T, Narasimhan B, et al. Diagnosis of multiple cancer types by shrunken centroids of gene expression. Proc Natl Acad Sci U S A, 2002, 99: 6567-6572.
  • 9Jay C, NemunatitisJ, Chen P, et al. miRNA profiling for diagnosis and prognosis of human cancer. DNA Cell Biol, 2007, 26 : 293 -270.
  • 10Gartel AL, Kandel ES. miRNAs: Little known mediators of oncogenesis. Semin Cancer Biol, 2008, 18 : 103-110.

二级参考文献16

  • 1Jemal A, Tiwari RC, Marray T, et al. Cancer statistics 2004 CA Cancer J Clin ,2004, 54:8-29.
  • 2Maroun J, Ng E, Berthelot JM, et al. Lifetime costs of colon and rectal cancer management in Canada. Chronic Dis Can, 2003,24:91-101.
  • 3Fearon ER, Vogelstein B. A genetic model for colorectal tumourigenesis. Cell,1990,61:759-765.
  • 4Lynch HT, Smyrk TC, Watson P,et al. Genetics,natural history, tumour spectrum, and pathology of hereditary nonpolyposis colorectal cancer:an updated review. Gastroenterology,1993,104:1535-1549.
  • 5Ionov Y,Peinado MA, Malkhosyan S, et al. Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis. Nature, 1993,363:558-561.
  • 6Papadopoulos N, Nicolaides NC, Wei YF, et al. Mutation of a mutL homolog in hereditary colon cancer. Science, 1994,263:1625-1629.
  • 7Markowitz S, Wang J, Myeroff L, et al.Inactivation of the type TGF-β receptor in colon cancer cells with microsatellite instability. Science, 1995,268:1336-1337.
  • 8Kane MF, Loda M, Gaida GM, et al. Methylation of the hMLH1 promoter correlates with lack of expression of hMLH1 in sporadic colon tumors and mismatch repair-defective human tumor cell line. Cancer Res, 1997,57:808-811.
  • 9Ahuja N, Mohan AL, Li Q, et al. Association between CpG island and microsatellite instability in colorectal cancer. Cancer Res, 1997,57:3370-3374.
  • 10Toyota M. CpG island methylator phenotype in colorectal cancer. Proc Natl Acad Sci USA,1999,96:8681-8686.

共引文献21

同被引文献41

引证文献4

二级引证文献22

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