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©2014 Baishideng Publishing Group Co.
World J Gastroenterol. Apr 21, 2014; 20(15): 4316-4328
Published online Apr 21, 2014. doi: 10.3748/wjg.v20.i15.4316
Published online Apr 21, 2014. doi: 10.3748/wjg.v20.i15.4316
Figure 3 High efficiency of Sendai virus/dF/green fluorescent protein vectors to HeLa cells and Sendai virus/dF/green fluorescent protein vectors indicates significant cell growth inhibition with apoptosis.
A: HeLa cells were infected with a 10 MOI of SeV/dF/FIR virus vector and cultured in DMEM for 3 d (72 h). The same amount of 10 MOI SeV/dF/GFP was also used to infect the control. As shown in the left lower panel, SeV/dF/GFP infected almost 100% cells (green). Under these conditions, SeV/dF/FIR significantly inhibited cell growth as shown in the left upper panel. Mock and 10 MOI SeV/dF/GFP showed no cell growth inhibition as seen in the right upper and lower panels; B: HeLa cells infected by 10 MOI SeV/dF/FIR for 3 d showed significant cell damage revealed by the APO Percentage apoptosis assay™, compared to mock or the same conditions of SeV/dF/GFP virus infected HeLa cells. 5 mmol/L H2O2 was used as a positive control. FIR: FBP Interacting Repressor; FBP: FUSE-Binding protein; FUSE: Far Upstream Element; SeV: Sendai virus; GFP: Green fluorescent protein; MOI: Multiplicity of infection.
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Citation: Matsushita K, Shimada H, Ueda Y, Inoue M, Hasegawa M, Tomonaga T, Matsubara H, Nomura F. Non-transmissible Sendai virus vector encoding
c-myc suppressor FBP-interacting repressor for cancer therapy. World J Gastroenterol 2014; 20(15): 4316-4328 - URL: https://www.wjgnet.com/1007-9327/full/v20/i15/4316.htm
- DOI: https://dx.doi.org/10.3748/wjg.v20.i15.4316