SKA3 promotes lung adenocarcinoma metastasis through the EGFR PI3K-Akt axis

被引:34
|
作者
Hu, Dan-dan [1 ]
Chen, Hai-ling [2 ]
Lou, Li-ming [1 ]
Zhang, Hong [1 ]
Yang, Guo-liang [3 ]
机构
[1] Zhejiang Chinese Med Univ, Zhejiang Prov Zhongshan Hosp, Dept Resp Med, Affiliated Hosp 3, Hangzhou 310000, Zhejiang, Peoples R China
[2] Zhejiang Chinese Med Univ, Guangxing Hosp, Dept Resp Med, Affiliated Hosp, Hangzhou 310000, Zhejiang, Peoples R China
[3] Zhejiang Integrated Trat & Western Med Hosp, Intern Med Oncol, Hangzhou 310000, Zhejiang, Peoples R China
基金
浙江省自然科学基金;
关键词
CANCER STATISTICS; COMPLEX; EMT; LOCALIZATION; SNAIL; AKT;
D O I
10.1042/BSR20194335
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The processes that lead to lung adenocarcinoma (LUAD) metastasis are poorly characterized. Spindle and kinetochore associated complex subunit 3 (SKA3) plays a key role in cervical cancer development, but its contribution to LUAD is unknown. Here, we found that SKA3 is overexpressed in LUAD and its expression correlates with lymph node metastasis and poor prognosis. SKA3 silencing experiments identified SKA3 as an oncogene that promotes the metastasis of LUAD cell lines and tissues. SKA3 was found to induce the expression of matrix metalloproteinase (MMP)-2, -7, and -9, which activate PI3K-AKT. SKA3 was also found to bind and activate EGFR to activate PI3K-AKT. In summary, we identify a role for SKA3 in LUAD metastasis through its ability to bind EFGR and activate PI3K-AKT signaling.
引用
收藏
页数:9
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