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Anti-tumor effect of thalidomide and paclitaxel on hepatocellular carcinoma in nude mice

机译:沙利度胺和紫杉醇对裸鼠肝细胞癌的抗肿瘤作用

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Background Thalidomide is reviving for its antiangiogenic effect on corneal neovascularization models. Recently, it has been employed in tumor research in several types of solid carcinomas. However, its effect on hepatocellular carcinoma ( HCC) has not yet been clarified. Methods A total of 48 nude mice bearing human HCC with a high metastatic potential were randomly divided into 4 groups. Thalidomide (200 mg/kg), paclitaxel (13 mg/kg) , or their combination, which was dissolved in 0. 5% sodium carboxyl methyl cellulose (CMC) suspension, was intraperitoneally injected in each group since the second day of the establishment of animal model. The group simply administered with 0. 5% CMC was set as placebo-control. The mice were sacrificed on the 30th day, for the measurement of tumor size, weight and metastasis in the lungs. The levels of CD_(34) and endothelial growth factor (VEGF) mRNA in tumor tissues were detected by immunohistochemistry and semiquantitative RT-PCR, respectively, and microvessel density (MVD) was evaluated. Results No statistical difference was found in tumor weight and volume between the thalidomide group and control ( P > 0. 05 ). Paclitaxel showed a growth-inhibiting effect on tumors ( P < 0. 05 ). The value of MVD and VEGF mRNA and metastases to the lungs in each group were lower than those in the placebo-control group ( P < 0. 05 ) ; such difference in the combination group was statistically significant ( P < 0. 05 ). Conclusions Paclitaxel, but not thalidomide, has significant growth inhibitory effect on tumors, but both significantly inhibit angiogenesis and metastasis of human HCC in nude mice, such effects of paclitaxel can be amplified by thalidomide.
机译:背景沙利度胺因其对角膜新生血管模型的抗血管生成作用而得以复兴。近来,它已被用于几种类型的实体癌的肿瘤研究中。但是,其对肝细胞癌(HCC)的作用尚未阐明。方法将48只具有高转移潜能的人肝癌裸鼠随机分为4组。自成立第二天起,将沙利度胺(200 mg / kg),紫杉醇(13 mg / kg)或它们的组合溶于0. 5%羧甲基纤维素钠(CMC)悬浮液中,每组腹膜内注射。动物模型。单纯用0. 5%CMC给药的组设为安慰剂对照。在第30天处死小鼠,以测量肿瘤大小,重量和在肺中的转移。分别通过免疫组织化学和半定量RT-PCR检测肿瘤组织中CD_(34)和内皮生长因子(VEGF)mRNA的水平,并评估微血管密度(MVD)。结果沙利度胺组与对照组的肿瘤重量和体积无统计学差异(P> 0. 05)。紫杉醇显示出对肿瘤的生长抑制作用(P <0. 05)。各组MVD和VEGF mRNA表达及肺转移均低于安慰剂对照组(P <0. 05);组合组的这种差异具有统计学意义(P <0. 05)。结论紫杉醇对沙丁胺醇具有明显的生长抑制作用,但对沙丁胺醇没有明显的抑制作用,但两者均能显着抑制人肝癌的血管生成和转移,沙利度胺可以增强紫杉醇的作用。

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