Methods: To identify the best condition, the cells were firstly electroporated without siRNA and cell viability

was determined by trypan blue and MTT assays. Then siRNA transfection in the best condition was performed. Western blot analysis was used for monitoring successful siRNA transfection. Results: The best condition for electroporation of this cell line was 220 volt and 975 µF in exponential decay using the Gene Pulser X cell electroporation system. Our data click this demonstrated that by using proper electroporation condition, DNA methyl Inhibitors,research,lifescience,medical transferase mRNA was silenced by 10 nmol DNMT1 siRNA in MDA-MB 468 cells when compared with negative control siRNA electroporation. Analysis of cell viability demonstrated that optimal electroporation condition resulted in 74% and 78% cell viability by trypan blue staining and MTT assay, respectively. Conclusion: Transfection of the MDA-MB-468 breast cancer cell line with siRNA in the obtained electroporation condition Inhibitors,research,lifescience,medical was successful and resulted

in effective gene silencing and high cellular viability. Key Words: Small interfering RNA, electroporation, breast cancer Introduction Small interfering RNA (siRNA) transfection is a valuable tool for evaluation Inhibitors,research,lifescience,medical of expression of many proteins and analysis of many pathways in the cells, and medical application.1 In mammalian cells, upon transfection of gene-specific siRNA, specific messages are destroyed resulting in a decrease in the corresponding protein Inhibitors,research,lifescience,medical level. This knockdown facilitates functional analysis of a gene product in the corresponding cells. Small interfering RNAs are short pieces of double stranded RNA (ds RNA) that exist naturally Inhibitors,research,lifescience,medical in the cells. They initiate the specific degradation of specific mRNAs,

and knockdown the expression of specific proteins. In this process, the antisense strand of the siRNA becomes a part of a multiprotein complex named RNA-induced silencing complex (RISC). The RISC identifies the corresponding mRNA, and cleaves it at a specific site. After degradation of mRNA, the expression of corresponding protein reduces.2 Transfection methods are used for delivery of RNA or DNA to the cells. They can be divided into chemical and physical methods. Chemical method includes liposoms or polycationic AV-951 polymers for introducing exogenous nucleic acid into the cultured cells.3,4 Transfection with this process has low efficiency in many experiments.5 Electroporation is a frequently-used physical method for nucleic acid transfer. In this method, the cells and nucleic acid suspended in a special buffer are subjected to high voltage pulses of electricity which generates a selleck chem potential difference across the membrane and induces temporary pores in the cell membrane.