期刊文献+

结直肠癌肝脏转移相关微小RNA224的研究 被引量:1

Study on miRNA-224 in Colorectal Cancer with Hepatic Metastasis
原文传递
导出
摘要 目的研究结直肠癌肝脏转移微小RNA(microRNA,miRNA)表达的差异以及相关特性。方法收集2009年4月至2010年11月期间首都医科大学附属复兴医院的10例伴或不伴肝脏转移的结直肠癌患者的肿瘤组织标本,应用miRNA芯片方法对2组样本的miRNA表达差异情况进行研究,并通过实时定量PCR对miRNA的芯片表达差异进行验证。结果芯片结果筛选出6种结直肠癌肝脏转移组较非转移组表达失调的miRNA(上调的miR-224、miR-1236和miR-622,下调的miR-155、miR-342-5p和miR-363),选取显著上调(即差异信号值大于500)的miR-224进行实时定量PCR验证,结果与芯片实验结果相一致。结论 miR-224可能通过调节其靶基因而在结直肠癌肝脏转移中起重要作用,miR-224可能成为未来结直肠癌生物标记或治疗方法的一个研究方向。 Objective To explore the microRNA(miRNA) expression changes and related miRNA characteristics of colorectal cancer(CRC) with hepatic metastasis by miRNA microarray.Methods The fresh specimens of primary CRC were collected in 10 patients during operation,which with hepatic metastasis or not.miRNA microarray analysis was performed to compare the miRNA expression levels in two groups.The different expression levels of miRNA were validated by quantitative real-time PCR analysis.Results A total of six dysregulated miRNAs were identified in the CRC patients with hepatic metastasis comparing with CRC patients without hepatic metastasis,including 3 up-regulated miRNAs(miR-224,miR-1236,and miR-622) and 3 down-regulated miRNAs(miR-155,miR-342-5p,and miR-363),and the quantitative real-time PCR result of miR-224 consisted with the microarray finding.Conclusions miR-224 may be involved in the process of CRC with hepatic metastasis pathogenesis.miR-224 would be a research direction on a new biomarker or therapic method in CRC with hepatic metastasis.
出处 《中国普外基础与临床杂志》 CAS 2013年第5期499-502,共4页 Chinese Journal of Bases and Clinics In General Surgery
基金 北京市教育委员会科技发展计划面上项目(项目编号:KM200910025022)~~
关键词 结直肠癌 微小RNA224 肝脏转移 基因芯片技术 Colorectal neoplasm microRNA-224 Hepatic metastasis miRNA microarray
  • 相关文献

参考文献26

  • 1Manfredi S, Lepage C, Hatem C, et al. Epidemiology and man- agement of liver metastases from colorectal cancer [ J]. Ann Surg, 2006, 244(2): 254-259.
  • 2Bolstad BM, Irizarry RA, Astrand M, et al. A comparison of normalization methods for high density oligonucleotide array data based on variance and bias [J]. Bioinformatics, 2003, 19(2): 185-193.
  • 3Livak K J, Schmittgen TD. Analysis of relative gene expre- ssion data using real-time quantitative PCR and the 2 6ACT method [J]. Methods, 2001,25(4): 402-408.
  • 4Cho WC. OncomiRs : the discovery and progress of microRNAs in cancers[J]. Mol Cancer, 2007, 6: 60.
  • 5Gregory PA, Bert AG, Paterson EL, et al. The miR-200 family and miR-205 regulate epithelial to mesenchymal trallsition by targe- ting ZEB1 and SIP1 [J] Nat Cell Biol, 2008, 10(5): 593-601.
  • 6Zhang YJ, He XJ, Liu YL, et al. microRNA-320a inhibits tumor invasion by targeting neuropilin 1 and is associated with liver metas- tasis in colorectal cancer [J] Oneol Rep, 2012, 27(3): 685-694.
  • 7Asangani IA, Rasheed SA, Nikolova DA, et al. MicroRNA-21 (miR-21) post-transcriptionally downregulates tumor suppressorPdcd4 and stimulates invasion, intravasation and metastasis in colorectal cancer [J]. Oncogene, 2008, 27(15): 2128-2136.
  • 8Wellner U, Schubert J, Burk UC, et al. The EMT-activator ZEB1 promotes tumorigenicity by repressing sternness-inhibiting microRNAs [J]. Nat Cell Biol, 2009, 11(12): 1487-1495.
  • 9张璐.在结肠腺癌中MicroRNA的表达方式与其预后和治疗效果的相关性[J].中国普外基础与临床杂志,2008,15(9):698-698. 被引量:1
  • 10张明,刘卫辉,尤楠,张福琴,窦科峰.7种microRNAs在原发性肝癌组织和癌旁组织间的差异表达及与血清肿瘤标志物水平的相关性研究[J].中国普外基础与临床杂志,2010,17(6):562-566. 被引量:8

二级参考文献49

共引文献15

同被引文献8

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