摘要
目的 探讨转录因子Twist、缺氧诱导因子(HIF)-1α在乳腺浸润性导管癌组织中的表达及其与上皮-间充质转化的关系.方法 采用免疫组织化学链霉菌抗生物素蛋白-过氧化物酶(SP)法检测90例乳腺浸润性导管癌组织及其对应癌旁组织标本中Twist、HIF-1α、E-钙黏蛋白(E-cadherin)及波形蛋白(Vimentin)的表达.结果 在乳腺癌组织中Twist、HIF-1α、E-cadherin和Vimentin的阳性率分别为73.3%、68.9%、15.6%和64.4%,癌旁组织中的阳性率分别为7.8%、8.9%、75.6%和34.4%.该4种蛋白在肿瘤组织中的表达率与癌旁组织之间差异均有统计学意义(P<0.05).Twist与HIF-1α的表达均与组织学分级和腋窝淋巴结转移有关(P<0.05).Twist与HIF-1α的表达呈正相关(P<0.05).Twist、HIF-1α的表达也均与E-cadherin的低表达和Vimentin的高表达密切相关(P<0.05).结论 Twist、HIF-1α和Vimentin在乳腺癌组织中呈高表达,而E-cadherin呈低表达.HIF-1α可能通过上调Twist表达,促进上皮-间充质转化发生,成为乳腺癌浸润转移的途径之一.
Objective To investigate the expression of Twist and hypoxia inducible factor-1α (HIF-1α) in invasive ductal carcinoma of breast and their relationships with epithelial-mesenchymal transition (EMT).Methods Expression levels of Twist,HIF-1α,E-cadherin and Vimentin in 90 cases of invasive ductal carcinoma tissues and corresponding adjacent tissues were detected by immunohistochemical staining of streptavid-in-peroxidase (SP) method.Results The positive expression rate of Twist,HIF-1 α,E-cadherin and Vimentin was 73.3%,68.9%,15.6% and 64.4% respectively in breast cancer tissues,and 7.8%,8.9%,75.6% and 34.4% respectively in adjacent tissues.The difference in positive rate between breast cancer tissues and adjacent tissues was statistically significant (P 〈 0.05).The expression levels of Twist and HIF-1α were correlated with histological grade and lymph node metastasis (P 〈 0.05).There was a positive correlation between expression levels of Twist and HIF-1α.The expression levels of Twist and HIF-1α were closely correlated with low expression of E-cadherin and high expression of Vimentin.Conclusion Twist,HIF-1α and Vimentin in breast cancer tissues showed higher expression,while E-cadherin lower expression.HIF-1α may promote the occurrence of EMT by up-regulating the expression of Twist,which makes it become one of the possible ways to promote the invasion and metastasis of breast cancer.
出处
《中华实验外科杂志》
CAS
CSCD
北大核心
2014年第10期2284-2286,共3页
Chinese Journal of Experimental Surgery
基金
河南省重点科技攻关计划资助项目(112102310088)