Role of PI3K/Akt signaling pathway in propofol-induced inhibition of migration and invasion ability of human non-small cell lung cancer H1975 cells / 中华麻醉学杂志

ABSTRACT

Objective To evaluate the role of phosphatidylinositol 3-kinase/serine-threonine kinase (PI3K/Akt) signaling pathway in propofol-induced inhibition of migration and invasion ability of human nonsmall cell lung cancer H1975 cells.Methods H1975 cells were divided into 4 groups (n=36 each) using a random number table method:control group (group C),20 μg/ml propofol group (group P),0.5 ng/ml PI3K/Akt signaling pathway activator insulin-like growth factor 1 (IGF-1) group (group IGF-1),and 20 μg/ml propofol plus 0.5 ng/ml IGF-I group (group P+IGF-1).The migration and invasion ability of H1975 cells was determined by wound healing assay and Transwell invasion assay,respectively.The expression of phosphorylated Akt (p-Akt) and matrix metalloproteinase-9 (MMP-9) was assessed by Western blot.Results Compared with group C,and the ability of migration and invasion was significantly reduced,and the expression of p-Akt and MMP-9 was down-regulated in group P,and the ability of migration and invasion was significantly enhanced,and the expression of p-Akt and MMP-9 was up-regulated in group IGF-1 (P＜0.05).Compared with group P,the ability of migration and invasion was significantly enhanced,and the expression of p-Akt and MMP-9 was up-regulated in group P+IGF-1 (P＜0.05).Compared with group IGF-1,the ability of migration and invasion was significantly reduced,and the expression of p-Akt and MMP-9 was down-regulated in group P+IGF-1 (P＜0.05).Conclusion The mechanism by which propofol inhibits migration and invasion ability of human non-small cell lung cancer H1975 cells is related to blocking PI3K/Akt signaling pathway.