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胃癌患者血清中miR-106a的表达及其临床意义 被引量:2

Detection of miR-106a in serum of patients with gastric cancer using a real-time quantitative RT-PCR platform and its clinical significance
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摘要 目的探讨胃癌患者血清miR-106a表达及其与临床病理特征之间的关系。方法采用实时定量RT-PCR方法检测21例胃癌患者及10例健康人血清中miR-106a表达的水平。结果实时定量RT-PCR方法能够检测到血清样本中微量miRNA的表达。21例胃癌患者miR-106a表达水平的中位数为0.34(0.17~0.69),10例健康人为0.63(0.27~1.0),两者差异有统计学意义(P=0.002)。在21例胃癌患者中,血清miR-106a表达水平与肿瘤分化程度有关,在低分化胃癌中的表达水平明显高于中分化胃癌(P=0.01);血清miR-106a表达水平亦与血清CA724相关(P=0.03),而与分期、性别、年龄无关(P>0.05)。结论采用实时定量RT-PCR方法检测血清中miR-106a的表达敏感可靠。血清miR-106a作为新的生物学指标对于胃癌的诊断具有一定的价值。 Objective To investigate the expression level of miR-106a in serum of patients with gastric cancer and its clinical significance. Methods Real-time quantitative RT-PCR (qRT-PCR) was performed in serum of 21 gastric cancer patients and 10 normal controls. Results Small amount of miR-lO6a was detected in serum using a qRT-PCR platform. The median expression level of miR-106a was 0. 34(0. 17-0. 69)in 21 gastric cancer patients and 0. 63(0. 27-1.0)in 10 normal controls. Serum miR-106a expression level in 21 patients was significantly lower than that in normal controls (P = 0. 002). Serum miR-106a expression was significantly associated with tumor differentiation( P =0. 01 ) and serum CA724( P = 0. 03 ). No correlation was found between serum miR-106a expression level and tumor stage, sex or age ( P 〉 0.05 ). Conclusion The qRT-PCR assay is reliable and sensitive for detecting the expression of miR-106a. Our data confirm a role for serum miR-106a as a novel cancer biomarker in gastric cancer.
出处 《临床肿瘤学杂志》 CAS 2012年第6期485-489,共5页 Chinese Clinical Oncology
基金 苏州市科技发展基金(SZD09127) 南京医科大学科技发展基金面上项目(NMU069)
关键词 miR-106a 胃癌 实时定量RT-PCR 血清 MiR-106a Gastric cancer Real-time quantitative RT-PCR Serum
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  • 1屈涛.血清半胱氨酸、维生素B2水平与食管癌及胃贲门癌相关[J].中国医学论坛报,肿瘤专刊,2001,.
  • 2Duffy MJ. Clinical uses of tumor markers: a critical review. Crit Rev Clin Lab Sci 2001; 38:225-262.
  • 3Thomas CM, Sweep CG. Serum tumor markers: past, state of the art, and future, lnt J Biol Markers 2001; 16:73-86.
  • 4Duffy MJ. Role of tumor markers in patients with solid cancers: a critical review. Eur J lntern Med 2007; 18:175-184.
  • 5Roulston JE. Limitations of tumour markers in screening. Br J Surg 1990; 77:961-962.
  • 6Esquela-Kerscher A, Slack FJ. Oncomirs - microRNAs with a role in cancer. Nat Rev Cancer 2006; 6:259-269.
  • 7Calin GA, Croce CM. MicroRNA signatures in human cancers. Nat Rev Cancer 2006; 6:857-866.
  • 8Chen C, Ridzon DA, Broomer A J, et al. Real-time quantification of microRNAs by stem-loop RT-PCR. Nucleic Acids Res 2005; 33:e179.
  • 9Tang F, Hajkova P, Barton SC, Lao K, Surani MA. MicroRNA expression profiling of single whole embryonic stem cells. Nucleic Acids Res 2006; 34:e9.
  • 10Hafner M, Landgraf P, Ludwig J, et al. Identification of microRNAs and other small regulatory RNAs using cDNA library sequencing. Methods 2008; 44:3-12.

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  • 1Sochor M, Basova P, Pesta M, Dusilkova N, Bartos J, Burda P, Pospisil V, Stopka T. Oncogenic mi- croRNAs: miR-155, miR-19a, miR-181b, and miR-24 enable monitoring of early breast cancer in serum. BMC Cancer 2014; 14:448 [PMID: 24938880 DOI- 10.1186/1471-2407-14-448].
  • 2Wang J, Huang SK, Zhao M, Yang M, Zhong JL, Gu YY, Peng H, Che YQ, Huang CZ. Identification of a circulating microRNA signature for colorectal cancer detection. PLoS One 2014; 9:e87451 [PMID: 24709885 DOI: 10.1371/journal.pone.0087451].
  • 3Wu C, Wang C, Guan X, Liu Y, Li D, Zhou X, Zhang Y, Chen X, Wang J, Zen K, Zhang CY, Zhang C. Diagnostic and prognostic implications of a serum miRNA panel in oesophageal squamous cell carci- noma. PLoS One 2014; 9:e92292 [PMID: 24651474 DOI: 10.1371/journal.pone.0092292].
  • 4Tsujiura M, Ichikawa D, Komatsu S, Shiozaki A, Takeshita H, Kosuga T, Konishi H, Morimura R, Deguchi K, Fujiwara H, Okamoto K, Otsuji E. Cir- culating microRNAs in plasma of patients with gas- tric cancers. Br J Cancer 2010; 102:1174-1179 [PMID: 20234369 DOI: 10.1038/sj.bjc.6605608].
  • 5Zhu C, Ren C, Han J, Ding Y, Du J, Dai N, Dai J, Ma H, Hu Z, Shen H, Xu Y, Jin G. A five-microRNA panel in plasma was identified as potential bio- marker for early detection of gastric cancer. Br J Cancer 2014; 110:2291-2299 [PMID: 24595006 DOI: 10.1038/bjc.2014.119].
  • 6Liu R, Zhang C, Hu Z, Li G, Wang C, Yang C, Huang D, Chen X, Zhang H, Zhuang R, Deng T, Liu H, Yin J, Wang S, Zen K, Ba Y, Zhang CY. A five- microRNA signature identified from genome-wideserum microRNA expression profiling serves as a fingerprint for gastric cancer diagnosis. Eur J Cancer 2011; 47:784-791 [PMID: 21112772 DOI: 10.1016/ j.ejca.2010.10.025].
  • 7Chen ZL, Zhao XH, Wang JW, Li BZ, Wang Z, Sun J, Tan FW, Ding DP, Xu XH, Zhou F, Tan XG, Hang J, Shi SS, Feng XL, He J. microRNA-92a promotes lymph node metastasis of human esophageal squamous cell carcinoma via E-cadherin. J Biol Chem 2011; 286:10725-10734 [PMID: 21148309 DOI: 10.1074/jbc.M110.165654].
  • 8Zhou T, Zhang G, Liu Z, Xia S, Tian H. Overexpres- sion of miR-92a correlates with tumor metastasis and poor prognosis in patients with colorectal cancer. Int J Colorectal Dis 2013; 28:19-24 [PMID: 22772712 DOI: 10.1007/s00384-012-1528-1].
  • 9Ferlay J,Shin HR,Bray F,et al.Estimates of worldwide burden of cancer in 2008:GLOBO-CAN 2008[J].Int J Cancer,2010,127(12):2893-2917.
  • 10Wang J,Wang Q,Liu H,et al.Micro RNA expression and its implication for the diagnosis and therapeutic strategies of gastric cancer[J].Cancer Lett,2010,297(2):137-143.

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