کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2775210 | 1152315 | 2011 | 8 صفحه PDF | دانلود رایگان |

Clinical trials of suicide gene therapy have achieved limited success, which suggests a need for improvement. Angiogenesis plays a crucial role in the progression of cancers, which is greatly regulated by vascular endothelial growth factor (VEGF).The current study was designed to evaluate the anti-tumor effects of VEGF siRNA in combination with fusion suicide gene yCDglyTK. Introduction of a VEGF-targeted small hairpin RNA (shVEGF) to CDTK/5-FC system could induce cell apoptosis more effectively and decrease micro vessel density in xenograft tissue, thus resulted in a significant tumor growth delay in SGC7901 xenografts. These findings for the first time suggest the potential of combination gene therapy using suicide gene therapy and anti-angiogenesis gene therapy.
► A triple-gene vector expressing VEGF-shRNA and fusion suicide gene yCDglyTK was constructed and delivered it into SGC7901 cells by calcium phosphate nanoparticles.
► The VEGF-targeted RNAi had a synergistic effect with suicide gene therapies.
► The combination gene therapy system could kill SGC7901 cells effectively in vitro and significantly suppress the tumor growth of SGC7901 xenografts in mice.
Journal: Experimental and Molecular Pathology - Volume 91, Issue 3, December 2011, Pages 745–752