高级搜索

miR-106a和miR-24-1在结肠癌中的表达及意义

李秋娴, 王晓华, 魏亚明, 黄颖烽

李秋娴, 王晓华, 魏亚明, 黄颖烽. miR-106a和miR-24-1在结肠癌中的表达及意义[J]. 肿瘤防治研究, 2012, 39(03): 303-306. DOI: 10.3971/j.issn.1000-8578.2012.03.015
引用本文: 李秋娴, 王晓华, 魏亚明, 黄颖烽. miR-106a和miR-24-1在结肠癌中的表达及意义[J]. 肿瘤防治研究, 2012, 39(03): 303-306. DOI: 10.3971/j.issn.1000-8578.2012.03.015
Li Qiuxian, Wang Xiaohua, Wei Yaming, Huang Yingfeng. Expression and Significance of miR-106a and miR-24-1 in Colon Cancer[J]. Cancer Research on Prevention and Treatment, 2012, 39(03): 303-306. DOI: 10.3971/j.issn.1000-8578.2012.03.015
Citation: Li Qiuxian, Wang Xiaohua, Wei Yaming, Huang Yingfeng. Expression and Significance of miR-106a and miR-24-1 in Colon Cancer[J]. Cancer Research on Prevention and Treatment, 2012, 39(03): 303-306. DOI: 10.3971/j.issn.1000-8578.2012.03.015

miR-106a和miR-24-1在结肠癌中的表达及意义

基金项目: 广东省医学科研基金资助项目(A2008517);广州市科技计划项目(2008J1-C171)
详细信息
    作者简介:

    李秋娴(1983-),女,硕士在读,主要从事结肠癌相关基因的研究

    通讯作者:

    王晓华,E-mail: xiaoh_wang@126.com

    魏亚明,E-mail: weiyaming@163.com

  • 中图分类号: R322.4;R735.3+5

Expression and Significance of miR-106a and miR-24-1 in Colon Cancer

  • 摘要: 目的 检测结肠癌与癌旁组织miR-106a和miR-24-1的表达差异及其与c-myc的表达是否具有关联性。方法选临床病理诊断明确的结肠癌患者,手术后取癌组织标本提取RNA,RT-PCR检测原癌基因c-myc在结肠癌组织与癌旁组织中的表达。TaqMan荧光定量PCR检测结肠癌与癌旁组织miR-106a和miR-24-1的表达差异。结果c-myc表达阳性的癌组织表达miR-106a要明显高于癌旁组织,其差异具有统计学意义(P<0.05);c-myc表达阴性的癌组织表达miR-106a要高于癌旁组织(P<0.05),结肠癌组织与癌旁组织miR-24-1的表达无差异。结论结肠癌组织c-myc阳性组和c-myc阴性组表达miR-106a均高于癌旁组织,miR-106a有可能作为结肠癌的筛查目标之一;结肠癌组织c-myc阳性组和c-myc阴性组表达miR-24-1与癌旁组织无差异,还需更多研究证实其与结肠癌的关系。

     

    Abstract: Objective To investigate the expression of miR-106a and miR-24-1 in both colon cancer and adjacent tissues,and analyze the relationship between the expression of miR-106a,miR-24-1 and c-myc gene. Methods To extract RNA from colon cancer tissues and their adjacent ones,detected the mRNA expression of c-myc by RT-PCR.The TaqMan fluorescence quantitative PCR was used to analyze the expression of the miR-106a and miR-24-1 in both colon cancer and adjacent tissues. Results The results showed that the expression of miR-106a in cancer tissues was higher than that in the adjacent tissues in the c-myc positive group(P<0.05),and the expression of miR-106a in cancer tissues was also higher than that in the adjacent tissues in the c-myc negative ones(P<0.05).The expression of miR-24-1 showed no difference either between cancer and adjacent tissues,or between positive and negative c-myc control. Conclusion The expression of miR-106a in both c-myc positive group cancer tissues and the c-myc negative ones were higher than that in adjacent tissues.miR-106a might be a blood screening target of colon cancer.There was no difference of the expression of miR-24-1 in both the c-myc positive group ones and the c-myc negative ones,which need more research to prove the relation between miR-24-1 and colon cancer.

     

  • [1] Zhou H,Guo JM,Lou YR,et al.Detection of circulating tumor cells in peripheral blood from patients with gastric cancer using microRNA as a marker [J].J Mol Med,2010,88(7):709-717.
    [2] He L,Hannon GJ.MicroRNAs: small RNAs with a big role in gene regulation [J].Nat Rev Genet,2004,5(7):522-531.
    [3] Kloosterman WP,Plasterk RH.The diverse functions of microRNAs in animal development and disease[J].Dev Cell,2006,11(4):441-450.
    [4] Perera RJ,Ray A.MicroRNAs in the search for understanding human diseases[J].Bio Drugs,2007,21(2):97-104.
    [5] Li QX,Huang YF,Wei YM,et al.Expression of stem cell-associated genes in colorectal cancer and SW620 cell line[J].Zhongguo Zu Zhi Gong Cheng Yan Jiu Yu Lin Chuang Kang Fu,2011,15(6):1015-1019.[李秋娴,黄颖烽,魏亚明,等.干细胞相关因子在大肠癌组织及SW620细胞株的表达[J].中国组织工程研究与临床康复,2011,15(6):1015-1019.]
    [6] Habib T,Park H,Tsang M,et al.Myc stimulates B lymphocyte differentiation and amplifies calcium signaling[J].J Cell Biol,2007,179(4):717-731.
    [7] Wang Z,Liu M,Zhu H,et al.Suppression of p21 by c-myc through members of miR-17 family at the post-transcriptional level[J].Int J Oncol,2010,37(5):1315-1321.
    [8] Schetter AJ,Leung SY,Sohn JJ,et al.MicroRNA expression profiles associated with prognosis and therapeutic outcome in colon adenocarcinoma[J].JAMA,2008,299(4): 425-436.
    [9] Sun F,Wang J,Pan Q,et al.Characterization of function and regulation of miR-24-1 and miR-31[J].Biochem Biophys Res Commun,2009,380(3): 660-665.
    [10] Zhao WY,Wang DD,Song MQ,et al.Role of microRNA-223 and its target gene oncogene c-myc in hepatocellular carcinoma pathogenesis[J].Zhonghua Gan Zang Bing Za Zhi,2011,19(2): 114-117.[赵文月,王冬冬,宋孟锜,等.微小RNA-223及其标靶基因c-myc在肝脏发病中的作用[J].中华肝脏病杂志,2011,19(2):114-117.]
    [11] Kuppers DA,Hwang HC,Jackson AL,et al.Effect of Xpcl1 Activation and p27 Loss on Gene Expression in Murine Lymphoma[J].PLoS One,2011,6(3): e14758.
    [12] Lal A,Navarro F,Maher CA,et al.miR-24 Inhibits cell proliferation by targeting E2F2,MYC,and other cell-cycle genes via binding to “seedless” 3′UTR microRNA recognition elements[J].Mol Cell,2009,35(5): 610-625.
    [13] Xiao B,Guo J,Miao Y,et al.Detection of miR-106a in gastric carcinoma and its clinical significance[J].Clin Chim Acta,2009,400(1-2):97-102
    [14] Tong AW,Nemunaitis J.Modulation of miRNA activity in human cancer: a new paradigm for cancer gene therapy[J].Cancer Gene Ther,2008,15(6): 341-355.
    [15] Diaz R,Silva J,Garcia JM,et al.Deregulated expression of miR-106a predicts survival in human colon cancer patients[J].Genes Chromosomes Cancer,2008,47(9): 794-802.
计量
  • 文章访问数:  2590
  • HTML全文浏览量:  25
  • PDF下载量:  637
  • 被引次数: 0
出版历程
  • 收稿日期:  2011-06-02
  • 修回日期:  2011-08-18
  • 刊出日期:  2012-03-24

目录

    /

    返回文章
    返回
    x 关闭 永久关闭