Guo Hui, Zhang Xin-Yu, Peng Jun, Huang Ying, Yang Yang, Liu Ying, Guo Xiao-Xi, Hao Qian, An Su, Xu Tian-Rui
Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, Yunnan, 650500, China; The First People's Hospital of Yunnan Province, Kunming, Yunnan, China.
Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, Yunnan, 650500, China.
Biochem Biophys Res Commun. 2018 Apr 15;498(4):932-939. doi: 10.1016/j.bbrc.2018.03.084. Epub 2018 Mar 15.
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.
肺癌仍然是全球癌症相关死亡的主要原因。RAF/MEK/ERK信号通路控制着许多基本的细胞功能,在肺癌发生过程中起关键作用。然而,调节该信号通路的蛋白质在很大程度上仍不为人知。在此,我们鉴定出一种新型的C-RAF结合蛋白RUVBL1,它通过抑制C-RAF蛋白丝氨酸259位点的磷酸化来激活RAF/MEK/ERK信号通路。RUVBL1在肺腺癌组织中的表达升高。此外,敲除RUVBL1可有效抑制A549细胞的增殖和侵袭。在体内实验中,RUVBL1缺陷显著降低了肺癌的肿瘤发生。总之,我们已经表明,RUVBL1可通过抑制C-RAF蛋白丝氨酸259位点的磷酸化来激活RAF/MEK/ERK信号通路,从而促进肺癌进展。因此,RUVBL1可能是肺癌治疗的一个新的治疗靶点。