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CH50多肽真核表达载体pCH510的构建、表达及体内趋化和抑瘤作用
引用本文:叶仕桥,冯作化,李东,张桂梅,张慧,黄波,肖徽. CH50多肽真核表达载体pCH510的构建、表达及体内趋化和抑瘤作用[J]. 中国肿瘤生物治疗杂志, 2001, 8(1): 23-26
作者姓名:叶仕桥  冯作化  李东  张桂梅  张慧  黄波  肖徽
作者单位:第四军医大学西京医院消化科西安710033
基金项目:本课题受国家自然科学基金(39870763)、教育部跨世纪人才培养计划基金资助
摘    要:目的:探讨血管内皮生长因子的表达与肿瘤血管生成的关系。方法:将VEGF165正、反义RNA表达载体导入人胃癌细胞,观察接种VEGF高表达和低表达胃癌细胞裸鼠移植瘤的生长情况,并对移植瘤进行组织学检查,检测其血管密度、组织增生及环死程度等变化。结果:VEGF正义转染细胞所致移植瘤的生长速度明显快于反义转染细胞所致的移植瘤;组织学检查发现,正义转染细胞移植瘤的血管密度显著高于的转染细胞所致的肿瘤。结论:血管皮生长因子通过启动血管生成而促进肿瘤的生长,阻断血管内皮生长因子的产生可以抑制肿瘤的生长。

关 键 词:血管内皮生长因子 血管生成 实体肿瘤 胃癌
收稿时间:2000-10-16
修稿时间:2000-10-08

Construction and Expression of Eukaryotic Expressing Vector pCH510 of Polypeptide CH50 and Its Chemotaxis and Antitumor Function by Transfection in vivo
YE Shiqiao,FENG Zuohu,LI Dong,ZHANG Guimei,ZHANG Hui,HUANG Bo and XIAO Hui. Construction and Expression of Eukaryotic Expressing Vector pCH510 of Polypeptide CH50 and Its Chemotaxis and Antitumor Function by Transfection in vivo[J]. Chinses Journal of Cancer Biotherapy, 2001, 8(1): 23-26
Authors:YE Shiqiao  FENG Zuohu  LI Dong  ZHANG Guimei  ZHANG Hui  HUANG Bo  XIAO Hui
Affiliation:Department of Medical Molecular Biology, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030;Department of Medical Molecular Biology, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030;Department of Medical Molecular Biology, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030;Department of Medical Molecular Biology, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030;Department of Medical Molecular Biology, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030;Department of Medical Molecular Biology, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030;Department of Medical Molecular Biology, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030
Abstract:Objective: To investigate the correlation between the expression of vascular endothelial growth factor(VEGF) and angiogenesis in tumor. Methods: VEGF 165 sense and antisense gene recombinants were introduced into human gastric cancer cells, respectively. Then the growth of transfected cells in nude mice and the microvascular density and histological change were examined. Results: The growth rate of tumor in nude mice inoculated with sense VEGF cells was markedly higher than that in nude mice inoculated with antisense-VEGF cells. In histological examination, the microvascular density in tumor caused by sense-VEGF cells was greatly higher than that in tumor caused by antisense VEGF cells. Conclusion: As starting angiogenesis, VEGF might promote the growth of tumor, and the inhibition of VEGF production might prevent solid tumor from growing.
Keywords:vascular endothelial growth factor   angiogenesis   solid tumor
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