4.7 Article

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

Journal

CELL DEATH & DISEASE
Volume 10, Issue -, Pages -

Publisher

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

Keywords

-

Categories

Funding

  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]

Ask authors/readers for more resources

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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available