Cui Zhengjun, Cen Ying, Zhang Jie
Department of Plastic and Burn Surgery, West China Hospital, Sichuan University, Chengdu Sichuan, 610041, P.R. China.
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2006 May;20(5):499-503.
To investigate the effect of Adenovirus-mediated averse vascular endothelial growth factor165(Ad-aVEGF165)on the growth of human melanoma cells(A375) in vivo and in vitro.
In vitro, the 100 multiplicity of infection of Adenovirus- mediated green fluorescent protein(Ad-GFP)and Ad-aVEGF165 were transfected into human endothelium cell of vessel304(ECV304) and A375. ECV304 cells were divided into 3 groups: A375 group, Ad-GFP group and Ad-aVEGF165 group. A375 cells were also divided into 3 groups: 1640 group, Ad-GFP group and Ad-aVEGF165 group. Their effects were analyzed by proliferation assay, cell cycle, and VEGF expression. In vivo, A375 cells were injected into the axilla of the nude mouse. When the tumor formed, they were transplanted into another 15 mice. After treatment, the tumor was excised for naked eye observation, HE observation and micro-vascular density (MVD) counting.
The cell supernatant fluid of A375 group and Ad-GFP group could stimulate ECV304 cell growth, but that of Ad-aVEGF165 group could inhibit the growth of ECV304 cell. All the A375 cells in 3 groups had the proliferation trend, showing no statistically significant difference (P>0.05). ECV304 cell proliferation index (PI) in Ad-aVEGF165 group reduced (P<0.05). There was no statistically significant difference (P>0.05) in the PI of A375 cell. The A375 cell integral optical densities were 234.41 +/- 13.8 in 1640 group, 222.73 +/- 3.67 in Ad-GFP group and 180.84 +/- 6.34 in Ad-aVEGF165 group. The tumor volume in Ad-aVEGF165 group was smaller than that in Ad-GFP group and PBS group at 2 weeks after operation, the trend became much obvious with the time delay. Ad-aVEGF165 brought to much tissue necrosis under HE stain. The MVD of PBS group, Ad-GFP group and Ad-aVEGF165 group were 65 +/- 10/view, 52 +/- 11/view and 30 +/- 6/ view, respectively.
In Vitro, Ad-VEGF165 gene could inhibited ECV304 cells' growth by weakening VEGF expression of A375 cells. In vivo, Ad-aVEGF165 could inhibit the growth of human melanoma from blocking micro-vascular.
探讨腺病毒介导的反义血管内皮生长因子165(Ad-aVEGF165)对人黑色素瘤细胞(A375)体内外生长的影响。
体外实验中,将腺病毒介导的绿色荧光蛋白(Ad-GFP)和Ad-aVEGF165以100感染复数转染到人血管内皮细胞304(ECV304)和A375细胞中。ECV304细胞分为3组:A375组、Ad-GFP组和Ad-aVEGF165组。A375细胞也分为3组:1640组、Ad-GFP组和Ad-aVEGF165组。通过增殖实验、细胞周期分析及VEGF表达分析其作用。体内实验中,将A375细胞接种于裸鼠腋窝。待肿瘤形成后,再移植到另外15只小鼠体内。处理后,切除肿瘤进行肉眼观察、HE观察及微血管密度(MVD)计数。
A375组和Ad-GFP组细胞培养上清液可刺激ECV304细胞生长,而Ad-aVEGF165组可抑制ECV304细胞生长。3组A375细胞均有增殖趋势,差异无统计学意义(P>0.05)。Ad-aVEGF165组ECV304细胞增殖指数(PI)降低(P<0.05)。A375细胞PI差异无统计学意义(P>0.05)。1640组A375细胞积分光密度为2 +/ 13.8,Ad-GFP组为222.73 +/ 3.67,Ad-aVEGF165组为180.84 +/ 6.34。术后2周,Ad-aVEGF165组肿瘤体积小于Ad-GFP组和PBS组,且随时间延长该趋势更明显。HE染色显示Ad-aVEGF165导致较多组织坏死。PBS组、Ad-GFP组和Ad-aVEGF165组的MVD分别为65 +/ 10/视野、52 +/ 11/视野和30 +/ 6/视野。
体外实验中,Ad-VEGF165基因可通过减弱A375细胞VEGF表达抑制ECV304细胞生长。体内实验中,Ad-aVEGF165可通过阻断微血管抑制人黑色素瘤生长。