RUVBL1, a novel C-RAF-binding protein, activates the RAF/MEK/ERK pathway to promote lung cancer tumorigenesis

被引:19
|
作者
Guo, Hui [1 ,2 ]
Zhang, Xin-Yu [1 ]
Peng, Jun [2 ]
Huang, Ying [1 ]
Yang, Yang [1 ]
Liu, Ying [1 ]
Guo, Xiao-Xi [1 ]
Hao, Qian [1 ]
An, Su [1 ]
Xu, Tian-Rui [1 ]
机构
[1] Kunming Univ Sci & Technol, Fac Life Sci & Technol, Kunming 650500, Yunnan, Peoples R China
[2] First Peoples Hosp Yunnan Prov, Kunming, Yunnan, Peoples R China
关键词
RUVBL1; C-RAF kinase; Lung cancer; A549; cells; CYSTEINE-RICH DOMAIN; REGULATES RAF-1; KINASE ACTIVATION; PROGRESSION; REPTIN; ERK1/2;
D O I
10.1016/j.bbrc.2018.03.084
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
Lung cancer remains the leading cause of cancer-related deaths in the world. The RAF/MEK/ERK pathway controls many fundamental cellular functions and plays key roles in lung carcinogenesis. However, the proteins that regulate this pathway remain largely unknown. Here, we identified a novel C-RAF-binding protein, RUVBL1, which activates the RAF/MEK/ERK pathway by inhibiting phosphorylation of the C-RAF protein at serine 259. RUVBL1 expression was elevated in lung adenocarcinoma tissues. In addition, knocking out RUVBL1 effectively inhibited the proliferation and invasion of A549 cells. In vivo experiments, RUVBL1 deficiency significantly decreased the tumorigensis of lung cancer. In conclusion, we have shown that RUVBL1 could activate the RAF/MEK/ERK pathway by inhibiting phosphorylation of the C-RAF protein at serine 259, to promote lung cancer progression. Therefore, RUVBL1 could represent a novel therapeutic target for lung cancer treatment. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:932 / 939
页数:8
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