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

被引:28
作者
Huang, Jun [1 ,2 ]
Lo, U-Ging [3 ]
Wu, Shiqi [1 ]
Wang, Bin [1 ]
Pong, Rey-Chen [3 ]
Lai, Chih-Ho [4 ]
Lin, Ho [5 ]
He, Dalin [1 ]
Hsieh, Jer-Tsong [3 ,6 ]
Wu, Kaijie [1 ]
机构
[1] Xi An Jiao Tong Univ, Affiliated Hosp 1, Dept Urol, Xian, Shaanxi, Peoples R China
[2] Cent South Univ, Xiangya Hosp 2, Dept Urol, Changsha, Hunan, Peoples R China
[3] Univ Texas Southwestern Med Ctr Dallas, Dept Urol, Dallas, TX 75390 USA
[4] Chang Gung Univ, Coll Med, Grad Inst Biomed Sci, Dept Microbiol & Immunol, Taoyuan, Taiwan
[5] Natl Chung Hsing Univ, Dept Life Sci, Taichung, Taiwan
[6] Kaohsiung Med Univ, Dept Biotechnol, Kaohsiung, Taiwan
基金
中国国家自然科学基金;
关键词
INTERCELLULAR-ADHESION MOLECULE-1; POTENTIAL VALUE; CELL INVASION; METASTASIS; CARCINOMA; MIGRATION; RECOGNITION; EXPRESSION; PROTEIN; GROWTH;
D O I
10.1038/s41419-019-1669-z
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页数:12
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