4.7 Article

The roles and mechanism of IFIT5 in bladder cancer epithelial-mesenchymal transition and progression

期刊

CELL DEATH & DISEASE
卷 10, 期 -, 页码 -

出版社

SPRINGERNATURE
DOI: 10.1038/s41419-019-1669-z

关键词

-

资金

  1. National Natural Science Foundation of China [NSFC 81572516]
  2. International Science and Technology Cooperation and Exchange Program in Shaanxi Province [2016KW-021]
  3. First Affiliated Hospital of Xi'an Jiaotong University [15YB08]

向作者/读者索取更多资源

The prognosis of bladder cancer (BCa) depends on several key factors including anatomical site, tumor grade, and stage. In general, muscle-invasive bladder cancer (MIBC) is associated with higher incidence of distant metastasis compared with Non-muscle-invasive bladder cancer (NMIBC). Treatment outcome of the patients with metastatic BCa has been very poor with similar to 15% of overall survival rate. Thus, it is apparently important to understand the underlying biology for metastatic progression of BCa. Although epithelial-mesenchymal transition (EMT) has long been implicated in BCa metastasis and treatment resistance, the underlying mechanism is not fully understood. In this study, we have identified that the expression of interferon induced protein with tetratricopeptide repeats 5 (IFIT5) is positively correlated with pathological characteristics, and predicts a poor prognosis of BCa patients. Since the function of IFIT5 in BCa has not yet been characterized, we demonstrate that IFIT5 can induce EMT, promote cell migration and invasion, and increase the expression of ICAM1 in BCa via down-regulation of mature miR-99a. Moreover, ICAM1 is shown as a direct target of miR-99a. Overall, we conclude that IFIT5 is a new oncogene in BCa.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据