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MiR-650 represses high-risk non-metastatic colorectal cancer progression via inhibition of AKT2/GSK3 beta/E-cadherin pathway  期刊论文  

  • 编号:
    f2aad972-a9cc-401b-8e9d-c02a0de679e9
  • 作者:
    Zhou, Chunxian(周春仙)#[1,2]Cui, Fengyun#[1]Li, Jiali#[1]Wang, Diyi[1];Wei, Yingze[1];Wu, Ying[1];Wang, Jiping[3];Zhu, Hongguang*[1]Wang, Shuyang*[1]
  • 语种:
    英文
  • 期刊:
    ONCOTARGET ISSN:1949-2553 2017 年 8 卷 30 期 (49534 - 49547) ; JUL 25
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  • 摘要:

    Although 5-year survival rate of non-metastatic colorectal cancer (CRC) is high, about 10% of patients in stage I and II still develop into metastatic CRC and eventually die after resection. Currently, there is no effective biomarker for predicting the prognosis of non-metastatic CRC in clinical practice. In this study, we identified miR-650 as a biomarker for prognosis prediction. We observed that the expression of miR-650 in tumor tissues had a positive association with overall survival. MiR-650 inhibited cell growth and invasion in vitro and in vivo. Furthermore, miR-650 targeted AKT2 and repressed the activation of the AKT pathway (AKT2/GSK3 beta/E-cadherin). Thus it induced the translocation of E-cadherin and beta-catenin in cancer cells. Our results highlight the potential of miR-650 as a prognostic prediction biomarker and therapeutic target in non-metastatic CRC via inhibition of the AKT2/GSK3 beta/E-cadherin pathway.

  • 推荐引用方式
    GB/T 7714:
    Zhou Chunxian,Cui Fengyun,Li Jiali, et al. MiR-650 represses high-risk non-metastatic colorectal cancer progression via inhibition of AKT2/GSK3 beta/E-cadherin pathway [J].ONCOTARGET,2017,8(30):49534-49547.
  • APA:
    Zhou Chunxian,Cui Fengyun,Li Jiali,Wang Diyi,&Wang Shuyang.(2017).MiR-650 represses high-risk non-metastatic colorectal cancer progression via inhibition of AKT2/GSK3 beta/E-cadherin pathway .ONCOTARGET,8(30):49534-49547.
  • MLA:
    Zhou Chunxian, et al. "MiR-650 represses high-risk non-metastatic colorectal cancer progression via inhibition of AKT2/GSK3 beta/E-cadherin pathway" .ONCOTARGET 8,30(2017):49534-49547.
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