TRAF5蛋白在乳腺癌中的表达  

Expression of TRAF5 Protein in Breast Carcinoma

在线阅读下载全文

作  者:代文博[1] 米小轶[2] 刘楠[2] 林红[1] 王岩岩[1] 曾亮[3] 

机构地区:[1]沈阳市第一人民医院病理科,辽宁沈阳110041 [2]中国医科大学病理学教研室 [3]沈阳医学院基础医学院解剖学教研室

出  处:《沈阳医学院学报》2014年第1期10-12,共3页Journal of Shenyang Medical College

摘  要:目的:探讨肿瘤坏死因子受体相关因子5(tumor necrosis factor receptor-associated factor 5,TRAF5)在正常乳腺组织、乳腺癌组织及不同侵袭能力乳腺癌细胞系中的表达情况,并分析其与微血管密度的关系。方法:应用免疫组化方法分别检测TRAF5和CD34在70例乳腺癌组织和14例正常乳腺组织中的表达,并计数微血管密度。应用Western blot方法检测TRAF5在乳腺癌细胞系MDA-MB-231(高侵袭)和MCF-7(低侵袭)中的表达。结果:TRAF5表达于正常乳腺导管上皮细胞和乳腺癌肿瘤细胞胞浆内。其在正常乳腺组织、非浸润性导管癌、浸润性导管癌中的阳性表达率逐渐升高,但差异无统计学意义(P>0.05)。TRAF5在乳腺癌高侵袭细胞系中的表达量高于低侵袭细胞系,但差异无统计学意义(P>0.05)。乳腺浸润性导管癌中,TRAF5阳性表达的微血管密度明显高于阴性表达组(P<0.05)。结论:在浸润性导管癌中,TRAF5表达与微血管密度有关。Objective: To investigate the expression of tumor necrosis factor receptor-associated factor 5 (TRAF5) in normal breast, breast carcinoma tissue, and cell lines with different invasive ability and the relations between TRAF5 and microvessel density (MVD). Methods: The expression of TRAF5 and CD34 in 70 specimens of breast carcinoma and 14 specimens of normal breast tis- sues was detected by SP immunohistochemistry separately, and MVI) was counted. The expression of TRAF5 in breast cancer cell lines, MDA-MB-231 with high invasive ability and MCF-7 with low invasive ability, was detected by Western blot. Results: TRAF5 was detected in cytoplasm of normal breast ductal epithelial ceils and breast carcinoma cells. The positive rates of TRAF5 were gradu- ally increased in normal breast tissues , in non-invasive ductal carcinoma and in invasive ductal carcinoma. But there was not signifi- cant difference (P 〉 O. 05 ). The protein level of TRAF5 was slightly higher in MDA-MB-231 cells than that in MCF-7 cells, but there was not significant difference (P 〉 0. 05). MVD of TRAF5 positive expression was more concentrated than negative expression in inva- sive ductal carcinoma ( P 〈 O. 05 ). Conclusion: The expression of TRAF5 is correlated to MVD in invasive ductal carcinoma.

关 键 词:肿瘤坏死因子受体相关因子5 乳腺肿瘤 免疫组化 

分 类 号:R730.21[医药卫生—肿瘤]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象