乳腺浸润性导管癌中HIF-1α与Twist1蛋白的表达与分析  被引量:1

Expression and analysis of HIF - 1 α and Twistl Proteins in invasive ductai carcinoma of breast

在线阅读下载全文

作  者:吴狄[1] 李荣[1] 罗荣城[1] 

机构地区:[1]南方医科大学南方医院肿瘤中心,广州510515

出  处:《实用肿瘤学杂志》2013年第2期144-148,共5页Practical Oncology Journal

摘  要:目的探讨乳腺浸润性导管癌中HIF-1α、Twist2蛋白表达及其临床意义。方法采用免疫组织化学SP法检测41例乳腺浸润性导管癌患者的癌组织与配对癌旁正常乳腺组织中HIF-1α与Twistl蛋白的表达情况。结果癌组织中HIF—1α与Twistl的阳性表达率明显高于癌旁正常乳腺组织(HIF-1α:78.0%vs19.5%,P〈0.001;Twistl:63.4%vs.12.2%,P〈0.001)。在癌组织中,HIF-1α与Twistl的表达分别与TNM分期呈正相关(HIF-1α:r=0.322,P=0.04;Twist1:r=0.430,P=0.005),HIF-1α与Twist1蛋白的表达呈正相关(r=0.331,P=0.034)。结论乳腺浸润性导管癌中HIF-1α.与Twist1蛋白呈高表达,且两者具有相关性,两者在乳腺浸润性导管癌的发生发展过程中可能起着重要的作用。Objective The study investigated the expressions and significance of hypoxia - inducible factor- 1α( HIF- 1α )and Twist l in invasive ductal carcinoma of breast (IDC). Methods The expressions of HIF- lot and Twistl proteins were detected by immunohistochemistry streptavidin perotridase (SP)method in breast carcinoma tissue and paired para - carcinoma tissues of 41 patients with IDC. Results The positive ex- pression rates of HIF - 1α and Twistl proteins in breast carcinoma tissues were significantly higher than in paired para - carcinoma tissues ( HIF - 1α :78.0% vs. 19.5 %, P 〈 0.001 ; Twist1:63. 4% vs. 12.2%, P 〈 0. 001 ). In breast carcinoma tissues, the expressions of HIF - 1α and Twistl in breast carcinoma tissues were both positively correlated with the TNM stage(HIF - lot:r =0. 322,P =0.04;Twistl r =0.43 ,P =0. 005) ,and the expression of HIF - lot was positively correlated with the expression of Twistl ( ( r =0.336 ,P =0.019) ) in breast carcinoma tissues. Conclusion The overexpressions of HIF - lot and Twistl were found in IDC and their expressions were positively correlated. They might play an important role in the development of IDC.

关 键 词:乳腺癌 免疫组织化学 乏氧诱导因子-1 TWIST 

分 类 号:R737.9[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