Effect of AS_2O_3 on Gene Expression of VEGF and bFGF in ACC-2 Cells Line
Bin Zhang
Abstract
Bin Zhang
Abstract
Objective:To investigate the effect of As_2O_3 on salivary adenoid cystic carcinoma-2(ACC-2)ceils proliferation in vitro and expression of VEGF and bFGF of the cells.Methods:ACC-2 cells were cultured with As_2O_3 in different concentrations(0、2、4、6μmol/L)for different time(24h、48h、72h).Cytomorphology was observed by phasecontrast microscopy.As_2O_3 cytotoxity was deter-mined by MTr assay.Gene and protein expression of VEGF and bFGF were investigated by RT-PCR and Western blotting analysis respectively.Results:Proliferation of ACC-2 cells were markedly promoted 24h after As_2O_3 administration.However,As_2O_3 induced a dose-and time-dependent tumor cell proliferation. The results of RT-PCR revealed no significant difference between gene expression of VEGF and bFGF.A negative relationship between As_2O_3 concentration and protein product of these two cytokines were observed.Conclusion:(1)ACC- 2 ceils might be markedly depressed after 48 h by As_2O_3 administration in a time-and dose-dependenty reliable pattern. In contrast,the cells' proliferation could be promoted within 48 h.(2)As_2O_3 toxicity can decrease protein product of VEGF and bFGF apparently.So might depress vessel formation of ACC-2 cells.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective:To investigate the effect of As_2O_3 on salivary adenoid cystic carcinoma-2(ACC-2)ceils proliferation in vitro and expression of VEGF and bFGF of the cells.Methods:ACC-2 cells were cultured with As_2O_3 in different concentrations(0、2、4、6μmol/L)for different time(24h、48h、72h).Cytomorphology was observed by phasecontrast microscopy.As_2O_3 cytotoxity was deter-mined by MTr assay.Gene and protein expression of VEGF and bFGF were investigated by RT-PCR and Western blotting analysis respectively.Results:Proliferation of ACC-2 cells were markedly promoted 24h after As_2O_3 administration.However,As_2O_3 induced a dose-and time-dependent tumor cell proliferation. The results of RT-PCR revealed no significant difference between gene expression of VEGF and bFGF.A negative relationship between As_2O_3 concentration and protein product of these two cytokines were observed.Conclusion:(1)ACC- 2 ceils might be markedly depressed after 48 h by As_2O_3 administration in a time-and dose-dependenty reliable pattern. In contrast,the cells' proliferation could be promoted within 48 h.(2)As_2O_3 toxicity can decrease protein product of VEGF and bFGF apparently.So might depress vessel formation of ACC-2 cells.
Key concepts: Medicine, Molecular biology, In vitro, Cell culture, Gene expression, Blot, Vascular endothelial growth factor, Cell growth