| Snail-1 known as one of the important transcription factor is a mediator of survival and cell migration,
and expression is raised in numerous cancer types. Snail-1 gene may show a role in recurrence of several
cancers including bladder cancer by down-regulating E-cadherin, inducing an epithelial to mesenchymal
transition (EMT) and its related microRNAs (miRNAs). The aim of this study was to investigate
the effect of a specific Snail-1 siRNA on apoptosis and alter EMT related miRNAs of EJ-138 (bladder cancer)
cells. The cells were transfected with siRNAs using transfection reagent. The cytotoxic effects of
Snail-1 siRNA, on bladder cancer cells were determined using MTT assay. Relative Snail-1 mRNA levels
were measured by QRT- PCR, respectively. Apoptosis was measured by TUNEL test based on labeling of
DNA strand breaks. We also evaluated miR-29b, miR-21, and miR-203 expression by QRT-PCR to determine
alteration in miRNAs expression involved in EMT. Snail-1 siRNA significantly reduced mRNA expression
levels in 48 h after transfection at the concentration of 60pmol in bladder cancer cells. We also
showed that the silencing of Snail-1 led to the induction of apoptosis. miR-21 and miR-29b depression
have been shown in Snail-1 suppressed group in EJ-138 cells in vitro. These results propose that Snail-1
might play an important role in the progression of bladder cancer, and be a potential therapeutic target
for trigger apoptosis and suppression of EMT-related miRNAs in bladder cancer. |