Gao Zhen-Nan, Wei Yu-Quan, Yang Pi-Shan, Xu Xin, Zhao Hua-Qiang, Huan Xin, Kang Bing
State Key Laboratory of Biotherapy, Sichuan University, Chengdu City 610041, PR China.
Oral Oncol. 2007 May;43(5):477-83. doi: 10.1016/j.oraloncology.2006.05.009. Epub 2006 Sep 25.
The aim of the present study was to assess the anti-tumor effect of a defective adenovirus that expresses soluble vascular endothelial growth factor (VEGF) receptor FLT-1 (AdsFLT-1) in combination with cisplatin (cis-diamminedichloroplatinum, DDP) on human tongue carcinoma Tca8113 cell xenografts that had been pre-established in nude mice. In vitro, Tca8113 cells secreted soluble FLT-1 (sFLT-1) after infection with AdsFLT-1, and the conditioned medium from AdsFLT-1-treated Tca8113 cells seemed to inhibit VEGF-induced proliferation of human umbilical vein endothelial cells. The combined effects of sFLT-1 gene therapy and DDP chemotherapy was then studied in well-established Tca8113 xenografts. The concentration of sFLT-1 in serum reached a peak 8 days after intratumoral injection of AdsFLT-1. In these tumors, AdsFLT-1 intratumoral injections had only a small effect. Interestingly, when the cells were also exposed to DDP chemotherapy, significantly higher (P<0.05), and possibly synergistic, anti-tumoral effects were observed that were highly correlated to a marked reduction in intratumoral vascularization and an increase in tumor-cell apoptosis. Together, these data emphasize the potential of combining an anti-angiogenic gene therapy strategy with a destructive approach directed against the tumor cells to fight human tongue carcinoma.
本研究旨在评估表达可溶性血管内皮生长因子(VEGF)受体FLT-1的缺陷型腺病毒(AdsFLT-1)联合顺铂(顺二氯二氨铂,DDP)对已在裸鼠体内预先建立的人舌癌Tca8113细胞异种移植瘤的抗肿瘤作用。在体外,Tca8113细胞感染AdsFLT-1后分泌可溶性FLT-1(sFLT-1),且来自经AdsFLT-1处理的Tca8113细胞的条件培养基似乎能抑制VEGF诱导的人脐静脉内皮细胞增殖。随后在已建立的Tca8113异种移植瘤中研究了sFLT-1基因治疗与DDP化疗的联合效果。瘤内注射AdsFLT-1后8天血清中sFLT-1浓度达到峰值。在这些肿瘤中,瘤内注射AdsFLT-1仅有轻微作用。有趣的是,当细胞同时接受DDP化疗时,观察到显著更高(P<0.05)且可能具有协同作用的抗肿瘤效果,这与瘤内血管化显著减少和肿瘤细胞凋亡增加高度相关。总之,这些数据强调了将抗血管生成基因治疗策略与针对肿瘤细胞的破坏性方法相结合来对抗人舌癌的潜力。