| Literature DB >> 29545175 |
Hui Guo1, Xin-Yu Zhang2, Jun Peng3, Ying Huang2, Yang Yang2, Ying Liu2, Xiao-Xi Guo2, Qian Hao2, Su An4, Tian-Rui Xu5.
Abstract
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.Entities:
Keywords: A549 cells; C-RAF kinase; Lung cancer; RUVBL1
Mesh:
Substances:
Year: 2018 PMID: 29545175 DOI: 10.1016/j.bbrc.2018.03.084
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575