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川芎嗪抗大肠癌sw620裸鼠移植瘤血管生成及抑瘤机制的实验研究
作者:李雷宇 张俊华 张银旭 李伟  
单位:辽宁医学院
关键词:川芎嗪 大肠癌 移植瘤 血管生成  
分类号:
出版年·卷·期(页码):2010·29·第五期(519-523)
摘要:

目的 探讨川芎嗪对人大肠癌实体瘤及其血管生成的抑制作用与机制。方法 建立大肠癌sw620裸鼠移植瘤模型,随机分成5组:生理盐水组、川芎嗪低、中、高剂量组、恩度组。给药后检测移植瘤的体积和重量,观察移植瘤的病理形态学改变,并分别用免疫组化法和Western blot法检测移植瘤组织中CD34、VEGF、HIF-1α蛋白表达。结果 与生理盐水组相比,川芎嗪中、高剂量组大肠癌sw620移植瘤的体积和重量明显减少,其瘤体内CD34、VEGF、HIF-1α的表达明显降低。结论 川芎嗪能抑制大肠癌sw620裸鼠移植瘤的生长,其作用机制可能与改善肿瘤组织的乏氧状况,抑制肿瘤血管生成有关。

Objective To Investigate the Inhibition affects and the mechanism of tetramethylpyrazine on angiogenesis of solid tumor in mice. Methods Established the model of colorectal cancer sw620 xenograft in nude mice,they were randomly divided into five groups: NS group,the low, middle and high dose of tetramethylpyrazine group,Endostar group. Measuring tumor volume and weight after administration.Observed pathological changes in tumors .Immunohistochemistry and Western blot was used to detect tumor tissue expression of CD34, VEGF, HIF-1α. Results Compared with the NS group,colorectal cancer sw620 xenografts in the middle and high dose of tetramethylpyrazine grope significantly reduced the size and weight. CD34, VEGF, HIF-1α expression was significantly lower in the tumor.Conclusion Tetramethylpyrazine can inhibit colorectal cancer sw620 xenografts growth in nude mice,the mechanism of affect may be related to to improve the status of tumor tissue hypoxia and Inhibit tumor angiogenesis.

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