gene over-expression on apoptosis of gastric cancer cell lines SGC-7901.
Methods
The stable
let-7a
gene over-expressing SGC-7901 cells
SGC-7901/
let-7a
cells
were established using shRNA lentiviral vector methods. Real-time RT-PCR analysis was used to evaluate the expression level of let-7a mRNA. Cells apoptosis was assessed by flow cytometry.
Results
RT-PCR analysis revealed
let-7a
expression in SGC-7901/
let-7a
cells was significantly increased. Cellular apoptosis assay showed that over-expression of
let-7a
could increase apoptosis of SGC-7901 cells (
P=
0.002).
Conclusion
Up-regulating
let-7a
expression promoted apoptosis in SGC-7901 cells.
关键词
Keywords
references
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