›› 2011, Vol. 42 ›› Issue (4): 494-497.doi: 10.3969/j.issn.0529-1356.2011.04.013

• 细胞分子生物学 • 上一篇    下一篇

表没食子儿茶素-3-没食子酸酯抑制乳腺癌裸鼠移植瘤淋巴管生成

刘春玲;邓思浩;张雅芳*   

  1. 哈尔滨医科大学解剖学教研室,哈尔滨 150081
  • 收稿日期:2010-11-08 修回日期:2010-12-13 出版日期:2011-08-06
  • 通讯作者: 张雅芳

Epigallocatechin-3-gallate inhibits the lymphangiogenesis of breast carcinoma in xenograft nude mice

  1. Department of Anatomy,Harbin Medical University,Harbin 150081,China
  • Received:2010-11-08 Revised:2010-12-13 Online:2011-08-06
  • Contact: ZHANG Ya-fang

关键词: 表没食子儿茶素-3-没食子酸酯, 异位移植瘤, 血管内皮生长因子C, 淋巴管生成, 免疫组织化学, 裸鼠

Abstract: Objective To investigate effects of epigallocatechin-3-gallate(EGCG) on the lymphangiogenesis of transplanted breast carcinoma in mice. Methods First, to establish the models of transplanted tumors in nude mice, a total of 30 nude mice were randomly divided into 5 groups: Saline group,5-FU control group,20mg/kg EGCG group,10mg/kg EGCG group,5mg/kg EGCG group. Immunohistochemical staining method was used to detect the expression of VEGF-C and lymphatic vessel endothelium in transplanted breast carcinoma, and the lymphatic vessel endothelial hyaluronan receptor-1 (LYVE-1) was used as the specific lymphatic endothelial marker for detecting microvessel density and area of lymphatic vessels. The expression of VEGF-C protein level in transplanted breast carcinoma was observed by using Western blotting in the different groups. Results The immunohistochemical staining revealed that the expression of VEGF-C was significantly reduced in EGCG 10mg/kg, 20mg/kg in dose-dependant manner compared with saline group(EM>P/EM>0.05),the density and area of lymphatic vessels in 20mg/kg EGCG group was lower and less than that of the other groups(EM>P/EM>0.05). Western blotting showed that the expression of VEGF-C protein also was significantly reduced in 20mg/kg group compared with the saline group(EM>P/EM>0.05). Conclusion GCG can inhibit significantly the expression of VEGF-C and the lymphangiogensis of breas

Key words: Epigallocatechin-3-gallate, Xenograft, Vascular endothelial growth factor C, Lymphangiogensis, Immunohistochemistry, Nude mouse

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