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肿瘤坏死因子样凋亡微弱诱导剂在乳腺癌中的表达及其与微血管密度的关系
引用本文:郑英伟,米小轶,方长青,刘树立,刘楠,魏敏杰. 肿瘤坏死因子样凋亡微弱诱导剂在乳腺癌中的表达及其与微血管密度的关系[J]. 癌症, 2008, 27(11): 1177-1181
作者姓名:郑英伟  米小轶  方长青  刘树立  刘楠  魏敏杰
作者单位:中国医科大学基础医学院,病理学教研室,辽宁,沈阳,110001;中国医科大学基础医学院,药理教研室,辽宁,沈阳,110001
摘    要:背景与目的:目前,对于肿瘤坏死因子样凋亡微弱诱导剂(TNF-likeweak inducer of apoptosis,TWEAK)在乳腺癌中的表达存在争议,本研究探讨TWEAK在乳腺癌组织及不同侵袭能力乳腺癌细胞系中表达情况及其与微血管密度(microvessel density,MVD)的关系.方法:应用免疫组化SP法检测TWEAK在70例乳腺癌组织和30例癌旁非癌乳腺组织中的表达.应用Western blot法检测TWEAK在乳腺癌细胞系MCF-7(低转移)和MDA-MB-231(高转移)中的表达.应用ELISA方法检测TWEAK在乳腺癌细胞系MCF-7和MDA-MB-231中的分泌情况.结果:TWEAK在乳腺癌组织中表达(60%)明显高于癌旁非癌组织(6.67%),且在浸润性导管癌组织(76.67%)中表达明显高于导管内癌组织(42.85%,P=0.003).浸润性导管癌组织中MVD高于导管内癌(P<0.05).浸润性导管癌组织中TWEAK表达与MVD明显相关(r=0.611),导管内癌中不显著(r=0.015).MDA-MB-231细胞系表达TWEAK明显高于MCF-7细胞系(t=4.259,P=0.007).MDA-MB-231细胞系分泌可溶性TWEAK高于MCF-7细胞系(t=3.6504,P=0.006).结论:TWEAK的表达与乳腺癌侵袭能力相关.

关 键 词:TWEAK  乳腺肿瘤  微血管密度

Expression of TNF-like Weak Inducer of Apoptosis(TWEAK) and Its Relationship to Microvessel Density in Breast Cancer
ZHENG Ying-Wei,MI Xiao-Yi,FANG Chang-Qing,LIU Shu-Li,LIU Nan,WEI Min-Jie. Expression of TNF-like Weak Inducer of Apoptosis(TWEAK) and Its Relationship to Microvessel Density in Breast Cancer[J]. Chinese journal of cancer, 2008, 27(11): 1177-1181
Authors:ZHENG Ying-Wei  MI Xiao-Yi  FANG Chang-Qing  LIU Shu-Li  LIU Nan  WEI Min-Jie
Affiliation:ZHENG Ying-Wei1,MI Xiao-Yi1,FANG Chang-Qing1,LIU Shu-Li1,LIU Nan1,WEI Min-Jie21.Department of Pathology,Chinese Medical University,Shenyang,Liaoning,110001,P.R.China 2.Department of Pharmacology,P.R.China
Abstract:BACKGROUND & OBJECTIVE:The expression of TNF-like weak inducer of apoptosis(TWEAK) in breast cancer remains disputable.This study was to investigate the expression of TWEAK in breast cancer tissues and breast cancer cell lines with different invasive abilities,and the relationship of TWEAK with microvessel density(MVD).METHODS:Immunohistochemical S-P method was adopted to detect the expression of TWEAK in 70 specimens of breast cancer and 30 specimens of adjacent normal breast tissues.The protein expression...
Keywords:TWEAK
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