K-Ras-ERK1/2 accelerates lung cancer cell development via mediating H3K18ac through the MDM2-GCN5-SIRT7 axis

Context: H3(K18ac) is linked to gene expression and DNA damage. Nevertheless, whether H3(K18ac) participates in regulating Ras-ERK1/2-affected lung cancer cell phenotypes remains unclear. Objective: We explored the effects of H3(K18ac) on Ras-ERK1/2-affected lung cancer cell phenotypes. Material and methods: NCI-H2126 cells were transfected with, pEGFP-K-Ras(WT) and pEGFP-K-Ras(G12V/T35S) plasmids for 48?h, and transfection with pEGFP-N1 served as a blank control. Then H3(K18ac) and AKT and ERK1/2 pathways-associated factors were examined. Different amounts of the H3(K18Q) (0.5, 1, and 2??g) plasmids and Ras(G12V/T35S) were co-transfected into NCI-H2126 cells, cell viability, cell colonies and migration were analyzed for exploring the biological functions of H3(K18ac) in NCI-H2126 cells. The ERK1/2 pathway downstream factors were detected by RT-PCR and ChIP assays. The regulatory functions of SIRT7, GCN5 and MDM2 in Ras-ERK1/2-regulated H3(K18ac) expression were finally uncovered. Results: Ras(G12V/T35S) transfection decreased the expression of H3(K18ac) about 2.5 times compared with the pEGFP-N1 transfection group, and activated ERK1/2 and AKT pathways. Moreover, H3(K18ac) reduced cell viability, colonies, migration, and altered ERK1/2 downstream transcription in NCI-H2126 cells. Additionally, SIRT7 knockdown increased H3(K18ac) expression and repressed cell viability, migration and the percentage of cells in S phase by about 50% compared to the control group, as well as changed ERK1/2 downstream factor expression. Besides, Ras-ERK1/2 decreased H3(K18ac) was linked to MDM2-regulated GCN5 degradation. Conclusion: These observations disclosed that Ras-ERK1/2 promoted the development of lung cancer via decreasing H3(K18ac) through MDM2-mediated GCN5 degradation. These findings might provide a new therapeutic strategy for lung cancer.