Knockdown of CPEB4 expression suppresses cell migration and invasion via Akt pathway in non-small cell lung cancer

被引:15
|
作者
Hu, Jing [1 ]
Zhang, LiBin [1 ]
Chen, Qiang [1 ]
Lin, Jie [1 ]
Wang, ShaoBo [1 ]
Liu, Ri [1 ]
Zhang, WenJing [1 ]
Miao, Kun [1 ]
Shou, Tao [1 ]
机构
[1] First Peoples Hosp Yunnan Prov, Dept Med Oncol, 157 Jinbi Rd, Kunming, Yunnan, Peoples R China
关键词
CPEB4; invasion; migration; non-small cell lung cancer; COLORECTAL-CANCER; BREAST-CANCER; TRANSLATIONAL CONTROL; PROLIFERATION; PROGRESSION; ANGIOGENESIS; METAANALYSIS; METASTASIS; ACTIVATION; CARCINOMA;
D O I
10.1002/cbin.10930
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cytoplasmic polyadenylation element binding protein 4 (CPEB4) could be an important regulator in variety of cancers. However, the biological function and the underlying molecular mechanism of CPEB4 in non-small cell lung cancer (NSCLC) remains unknown. In this study, we investigated the metastasis role of CPEB4 in NSCLC cells, we knocked down CPEB4 using siRNA. Transwell migration assay and cell invasion assay on Matrigel were presented, and cell migration was also determined by scratch-healing assay. ROS generation were determined by fluorescence probe DCFH2-DA. The protein expression was assessed by ELISA and Western blot analysis. LY294002 were used to inhibit PI3K/Akt signaling. The data showed that knockdown of CPEB4 inhibited the migration and invasion of NSCLC. Moreover, silencing of CPEB4 reduced Snail and MMP-3 expression in vitro. We also indicated that CPEB4 knockdown increased the ROS expression. Furthermore, we found that silencing of CPEB4 decreased pAkt expression. Taken all together, our data demonstrated that silencing of CPEB4 induces ROS generation, thus suppressing the Akt expression, which finally prevents NSCLC cells invasion and migration. Therefore, CPEB4 may regard as a target to inhibit NSCLC invasion and metastasis through Akt pathway.
引用
收藏
页码:1484 / 1491
页数:8
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