BACKGROUND The epithelial-mesenchymal transition (EMT) has been shown to be involved in the process of invasion and
metastasis of
prostate cancer.
SIRT1 is the mammalian homologue of the silent information regulator 2 (Sir2) gene, and is abnormally expressed in
prostate cancer cells. Therefore, it is hypothesized that
SIRT1 mediates the invasion/metastatic ability of
prostate cancer via EMT regulation. This study thus investigated the effect of
SIRT1 gene on the invasion and migration of
prostate cancer cell line PC-3 via the small interference RNA (
siRNA) against
SIRT1. MATERIAL AND METHODS
SiRNA construct was transfected into PC-3 cells, which were tested for the cell migration and invasion ability by scratch assay and Transwell migration assay, respectively. Expression levels of
vimentin,
E-cadherin, and
N-cadherin were further quantified by Western blotting and RT-PCR. RESULTS Both
mRNA and
protein levels of
SIRT1 were depressed after
siRNA transfection, along with weakened migration and invasion ability of PC-3 cells. Elevated
E-cadherin and suppressed
N-cadherin and
vimentin were observed in those transfected cells. CONCLUSIONS The silencing of
SIRT1 gene in PC-3 cells can suppress the movement, migration, and invasion functions of
prostate cancer cells, possibly via the down-regulation of mesenchymal markers
vimentin and
N-cadherin accompanied with up-regulation of epithelial marker
N-cadherin, thus reversing the EMT process.