Yue Guangxing,Zhang Mingzhi,Zhang Xudong,Xu Weipeng,Chen Xinfeng,Chen Yucheng,Cao Ling,Yang Li,Sheng Yuqiao.Effect of shRNA interference targeting myeloid leukemia-1 gene on proliferation in lymphoma cell line[J].J Amry Med Univ (J Third Mil Med Univ),2012,34(12):1210-1213.
Yue Guangxing,Zhang Mingzhi,Zhang Xudong,Xu Weipeng,Chen Xinfeng,Chen Yucheng,Cao Ling,Yang Li,Sheng Yuqiao.Effect of shRNA interference targeting myeloid leukemia-1 gene on proliferation in lymphoma cell line[J].J Amry Med Univ (J Third Mil Med Univ),2012,34(12):1210-1213.DOI:
Effect of shRNA interference targeting myeloid leukemia-1 gene on proliferation in lymphoma cell line
Objective To explore the effect of lentivirus-mediated short hairpin RNA (shRNA) interference targeting myeloid leukemia-1 (Mcl-1) gene on the proliferation and apoptosis of lymphoma cell line SNK-6. Methods The shRNA targeting Mcl-1 gene was designed and the lentiviral vector carrying the shRNA was constructed. Lymphoma SNK-6 cells were transfected with the recombinant lentiviral vectors (shRNA group) and the blank lentiviral vectors (control group)
respectively. Real-time PCR and Western blotting were used to analyze the mRNA and protein expression of Mcl-1 gene in SNK-6 cells before and after transfection. MTT assay and flow cytometry were applied to detect the proliferation and apoptosis of the transfected SNK-6 cells
respectively. Results The shRNA targeting Mcl-1 gene was successfully inserted into the lentiviral vectors
which could effectively infect lymphoma SNK-6 cells. The mRNA and protein expression of Mcl-1 gene in the shRNA group significantly decreased as compared with those in the control group. The MTT assay results suggested that the proliferation of SNK-6 cells was significantly inhibited in the shRNA group as compared with that in the control group [(31.6±3.3)% vs (5.8±2.7)%
P0.01]. The flow cytometry showed that the apoptosis rate of the shRNA group was significantly higher than that of the control group [(28.9±2.1)% vs (5.3±1.5)%
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