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Angiogenesis in rabbit hepatic tumor after transcatheter arterial embolization

机译:经导管动脉栓塞术后兔肝肿瘤血管生成

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AIM: To investigate the effect of transcatheter arterial embolization (TAE) on angiogenesis of hepatic tumor. METHODS: 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. RESULTS: 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). CONCLUSION: TAE promotes the development of neovascularization of residual tumors through up-regulation of VEGF expression, possibly due to hypoxic insult.
机译:目的:探讨经导管动脉栓塞术(TAE)对肝肿瘤血管生成的影响。方法:将20只新西兰白兔随机分为两组,每组10只,并将VX2癌植入肝左内侧叶。 14天后,将硅导管插入患有VX2肝肿瘤的兔子的左肝动脉中,并使用Lipiodol(TAE组)或生理盐水(对照组)通过肝动脉进行输注。处理后7天处死兔子,并切除肿瘤组织。使用免疫组织化学检查血管内皮生长因子(VEGF)蛋白的表达和肿瘤的微血管密度(MVD)。用计算机辅助图像分析仪评估VEGF的染色强度。用逆转录聚合酶链反应(RT-PCR)检测肿瘤的VEGF mRNA表达。结果:TAE组MVD高于对照组(28.6±-10.6 vs 16.3±6.9,P <0.01)。 TAE后VEGF蛋白的表达增强。 TAE组VEGF的染色强度为0.162 + -0.018,明显高于对照组(0.142 + -0.01,P <0.01)。在mRNA水平上,TAE组的VEGF165 mRNA显着高于对照组(2.58 + -0.42对1.99 + -0.21,P <0.001)。 MVD与TAE组(r = 0.69,P <0.05)和对照组(r = 0.72,P <0.05)均与VEGF表达高度相关。结论:TAE通过上调VEGF表达促进残余肿瘤的新生血管形成,这可能是由于低氧损伤引起的。

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