Liao Xiao-Feng, Yi Ji-Lin, Li Xing-Rui, Deng Wei, Yang Zhi-Fang, Tian Geng
Department of General Surgery, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, Hubei Province, China.
World J Gastroenterol. 2004 Jul 1;10(13):1885-9. doi: 10.3748/wjg.v10.i13.1885.
To investigate the effect of transcatheter arterial embolization (TAE) on angiogenesis of hepatic tumor.
Twenty New Zealand White rabbits were randomly divided into two groups of 10 each and VX2 carcinoma was implanted in the left medial lobes of the livers. Fourteen days later, a silicon catheter was inserted into the left hepatic artery of rabbit with VX2 hepatic tumor and infusion was performed via the hepatic artery using Lipiodol (the TAE group) or saline (the control group). Rabbits were sacrificed 7 d after treatment and tumor tissues were excised. Expression of vascular endothelial growth factor (VEGF) protein and microvessel density (MVD) of tumors were examined using immunohistochemistry. The staining intensity of VEGF was evaluated with a computer-assisted image-analyzer. Reverse transcription-polymerase chain reaction (RT-PCR) was used to detect the VEGF mRNA expression of tumors.
MVD was higher in the TAE group compared with the control group (28.6+/-10.6 vs 16.3+/-6.9, P<0.01). Expression of VEGF protein was enhanced after TAE. The staining intensity of VEGF in the TAE group was 0.162+/-0.018, significantly higher than in the control group (0.142+/-0.01, P<0.01). At mRNA level, VEGF165 mRNA was significantly higher in the TAE group compared with the control group (2.58+/-0.42 vs 1.99+/-0.21, P<0.001). MVD was well correlated to VEGF expression in both the TAE group (r=0.69, P<0.05) and the control group (r=0.72, P<0.05).
TAE promotes the development of neovascularization of residual tumors through up-regulation of VEGF expression, possibly due to hypoxic insult.
探讨经导管动脉栓塞术(TAE)对肝肿瘤血管生成的影响。
将20只新西兰白兔随机分为两组,每组10只,在肝脏左内侧叶植入VX2癌。14天后,将硅胶导管插入患有VX2肝肿瘤的兔的肝左动脉,并通过肝动脉注入碘油(TAE组)或生理盐水(对照组)。治疗7天后处死兔子,切除肿瘤组织。采用免疫组织化学法检测肿瘤组织中血管内皮生长因子(VEGF)蛋白表达及微血管密度(MVD)。用计算机辅助图像分析仪评估VEGF的染色强度。采用逆转录聚合酶链反应(RT-PCR)检测肿瘤组织中VEGF mRNA表达。
TAE组MVD高于对照组(28.6±10.6 vs 16.3±6.9,P<0.01)。TAE后VEGF蛋白表达增强。TAE组VEGF染色强度为0.162±0.018,显著高于对照组(0.142±0.01,P<0.01)。在mRNA水平,TAE组VEGF165 mRNA显著高于对照组(2.58±0.42 vs 1.99±0.21,P<0.001)。TAE组和对照组MVD与VEGF表达均呈良好相关性(TAE组r=0.69,P<0.05;对照组r=0.72,P<0.05)。
TAE可能通过缺氧损伤上调VEGF表达,促进残留肿瘤新生血管形成。