摘要
AIM:To study the effects of cortactin on the tumor biology of SGC-7901 cells and identify the mechanism involved in the process.METHODS:Cell lines in which cortactin was stably overexpressed or knocked down as well as the respective control cell lines were established by standard molecular methods.The effects of cortactin on the proliferation,migration and invasion capacity of SGC-7901cells were assessed by the MTT assay,colony formation,flow cytometry,transwell migration and matrigel invasion.Nude mouse models were also used to assess the role of cortactin in the growth and metastasis of SGC-7901 cells in vivo.Western blotting analysis was performed to detect the expression of epidermal growth factor receptor(EGFR)and downstream molecules.RESULTS:Cell lines in which cortactin was stably overexpressed or knocked down as well as control cell lines were successfully established and designated as LV5-cortactin-SGC,LV5-SGC,LV3-shRNA-SGC and LV3-SGC.Cortactin overexpression promoted SGC-7901 cell migration(340.7±12.6 vs 229.1±23.2,P<0.01)and invasion(71.6±5.2 vs 48.4±3.6,P<0.01).Cortactin downregulation impaired SGC-7901 cell migration(136.2±19.8 vs 225±17)and invasion(29.2±5.2vs 49.6±3.8,P<0.01).The results from the MTT and colony formation assays results indicated increased LV5-cortactin-SGC cell proliferation and decreased LV3-shRNA-SGC cell proliferation compared to the control cells.Flow cytometry analysis demonstrated that cortactin overexpression promoted the proliferation index of SGC-7901 cells,and the results were reversed when cortactin was downregulated.Mouse tumor models confirmed that cortactin expression increased SGC-7901cell proliferation and metastasis in vivo.Western blotting analysis revealed that cortactin elevated EGFR expression and activated the downstream molecules.CONCLUSION:Cortactin expression promoted the migration,invasion and proliferation of SGC-7901 cells both in vivo and in vitro.The EGFR signaling pathway is mechanistically involved.
AIM: To study the effects of cortactin on the tumor biology of SGC-7901 cells and identify the mechanism involved in the process. METHODS: Cell lines in which cortactin was stably overexpressed or knocked down as well as the respective control cell lines were established by standard molecular methods. The effects of cortactin on the proliferation, migration and invasion capacity of SGC-7901 cells were assessed by the MTT assay, colony formation, flow cytometry, transwell migration and matrigel invasion. Nude mouse models were also used to assess the role of cortactin in the growth and metastasis of SGC-7901 cells in vivo. Western blotting analysis was performed to detect the expression of epidermal growth factor receptor (EGFR) and downstream molecules. RESULTS: Cell lines in which cortactin was stably overexpressed or knocked down as well as control cell lines were successfully established and designated as LV5-cortactin-SGC, LV5-SGC, LV3-shRNA-SGC and LV3SGC. Cortactin overexpression promoted SGC-7901 cell migration (340.7 +/- 12.6 vs 229.1 +/- 23.2, P < 0.01) and invasion (71.6 +/- 5.2 vs 48.4 +/- 3.6, P < 0.01). Cortactin downregulation impaired SGC-7901 cell migration (136.2 +/- 19.8 vs 225 +/- 17) and invasion (29.2 +/- 5.2 vs 49.6 +/- 3.8, P < 0.01). The results from the MTT and colony formation assays results indicated increased LV5-cortactin-SGC cell proliferation and decreased LV3shRNA-SGC cell proliferation compared to the control cells. Flow cytometry analysis demonstrated that cortactin overexpression promoted the proliferation index of SGC-7901 cells, and the results were reversed when cortactin was downregulated. Mouse tumor models confirmed that cortactin expression increased SGC-7901 cell proliferation and metastasis in vivo. Western blotting analysis revealed that cortactin elevated EGFR expression and activated the downstream molecules. CONCLUSION: Cortactin expression promoted the migration, invasion and proliferation of SGC-7901 cells both in vivo and in vitro. The EGFR signaling pathway is mechanistically involved. (c) 2014 Baishideng Publishing Group Co., Limited. All rights reserved.
基金
Supported by Grants from the Project of Shanghai Science and Technology Commission of China,No.10411968400
