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安体优I抑制肿瘤淋巴管生成的实验研究
引用本文:高文仓,杨平,谢长生,吴良村,冯媛,苗迎秋,郑丛龙. 安体优I抑制肿瘤淋巴管生成的实验研究[J]. 陕西肿瘤医学, 2009, 17(12): 2256-2259
作者姓名:高文仓  杨平  谢长生  吴良村  冯媛  苗迎秋  郑丛龙
作者单位:[1]大连大学附属新华医院,辽宁大连116021 [2]浙江省中医院,浙江杭州310000 [3]大连大学医学院,辽宁大连116000
基金项目:【基金项目】辽宁省自然科学基金资助项目(编号:20070036)
摘    要:目的:观察安体优I对615小鼠HCa—F肝癌淋巴道转移的影响,探讨其作用机理。方法:生理盐水、干扰素和安体优1分别作用于动物模型,3周后检测转移淋巴结计数及转移率;免疫组化检测VEGF—C和Flt-4,5’-Nase—ALP双重组织化学法检测淋巴管微密度。结果:模型组、0l—IFN组和中药组转移淋巴结计数分别为5.88±2.30、4.13zl:1.64和3.50±1.91个;淋巴结转移率分别为78.6%、61.1%和57.4%;微淋巴管密度分别为25.25±4.59、22.384-4.41和21.75±4.71;VEGF—c的阳性率分别为87.5%、25.0%和25.0%,Fit-4阳性率分别为100.O%、37.5%和50.0%,中药组与模型组比较有显著性差异(P〈0.05);结论:安体优I具有抑制615小鼠HCa—F肝癌淋巴道转移作用,其机制可能与下调淋巴管生成信号通路VEGF—c及其受体Fit-4的表达,抑制肿瘤淋巴管生成相关。

关 键 词:中医药疗法  淋巴道转移  淋巴管生成  血管内皮生长因子-C  血管内皮生长因子受体-3

The experiment research of inhibitory effect of ATU - I on lymphangiogenesis of HCa - F liver cancer in 615 mice
Affiliation:GAO Wen - cang , YANG Ping , XIE Chang - sheng, WU Liang -cun, FENG Yuan, MIAO Ying - qiu , ZHENG Cong - long( 1Xinhua Hospital Affdiated to Dalian University, Dalian 116021, China; 2 Zhejiang Province TCM Hospital, Hangzhou 310000, China ; 3 Medical School Dalian University , Dalian 116000, China.)
Abstract:Objective: To observe the inhibitory effect of ATU - I on lymphatic metastasis of HCa - F liver cancer in 615 mice. Methods: To treat the mice model with NS,α -IFN and ATU - I ,count the number of metastasized lymph node and rate of metastasis 3 weeks later; detect the expression of VEGF - C and Fh - 4 with immunohisto- chemical method; detect the micro - lymph duct density (MLD) with 5' - Nase - ALP double staining method. Re- suits : In Model group, α - IFN group and ATU - I group, the number of metastasized lymph node were 5.88 + 2.30, 4.13 ± 1.64 and 3.50 ± 1.91, the rates of metastasis of lymph node were 78.6% ,61.1% and 57.4% ;MLD were 25.25±4.59,22.38±4.41 and 21.75±4.71 ,the positive rates of VEGF - C were 87.5% ,25.0% and 25.0% ,the positive rates of Fit -4 were 100.0% ,37.5% and 50.0% ,comparing with Model group,there was a significance different in ATU - I group(P 〈0.05). Conclusion: There is the effect of inhibition to the metastasis of lymphdute of HCa - F liver cancer in 615 mice treated with ATU - I,and the mechanism relates with down regulate of VEGF - C/ Flt- 4 and inhibition of lymphangiogenesis of liver cancer.
Keywords:TCM - therapy  lymphatic metastasis  lymphangiogenesis  VEGF - C  Flt - 4
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