ABSTRACT
Breast cancer is the most prevalent cancer and the second leading cause of cancer death in women. Because of side effects of current treatments, researchers are looking for methods with less possible side effects and highest rate of destruction of cancer cells without influencing healthy cells. Based on this, cold atmospheric plasma [CAP], is used on MCF-7 breast cancer cells. In this method, electromagnetic waves are used for destruction and death of cells. The aim of this study was to evaluate the treatment of breast cancer using CAP. In this study, cold atmospheric plasma [CAP] with helium gas and oxygen was used for treatment of breast cancer cells [MCF-7] in different times and with using MTT assay to determine viability percentage of treated cells. Data were analyzed by one way ANOVA using SPSS software. Viability percentage of cancer cells treated with CAP was significantly reduced compared to cancer cells not treated with plasma. Optimal treatment time of CAP for cancer cells was 45s. Cold atmospheric plasma can be considered as useful method for breast cancer cells treatment
ABSTRACT
The ability to reducing death due to apoptosis and maintaining extensive levels on cell viability under serum free media in cell culture are important subjects in production of recombinant proteins. Insulin-like growth factor-I [IGF-I], is the growth factor of choice for mammalian cell proliferation in serum-free culture. In addition to its mitogenic activity, it has antiapoptotic activity protecting cultures from diverse death inducing stimuli. In this study, the effect of different concentrations of IGF-I examined on CHO-K1 [Chinese hamster ovary K1 cells] cell line for 24 and 48 hours. In this experimental study, the cell line was cultivated in DMEM supplemented with 10% fetal bovine serum [FBS]. Apoptosis process was induced in cells by methotrexate, serum was removed and then 10-50 ng/ml concentrations of IGF-I were added. Apoptosis was assessed by caspase 3 detection kit and cell proliferation and viability determined by MTT assay. Caspase 3 activity decreased significantly by increasing concentrations of IGF-I. In the highest concentration of IGF-I [50 ng/ml], 1.7 and 1.4 equal decreases of caspase 3 activities, compared with negative control group, were noted after 24 and 48 hours, respectively. It confirmed antiapoptotic activity of growth factor to maintain viability and protect cultures from apoptotic inducing stimuli [methotrexate]. IGF-I, as antiapoptotic factor, decreased programmed death of CHO-K1 cells in apoptotic induced conditions