摘要
目的:探讨IQGAP1(IQ motif containing GTPase activating protein 1)在乳腺癌组织中的表达及意义。方法:采用免疫组织化学链霉菌抗生物素蛋白-过氧化物酶(S-P法)染色法检测IQGAP1在乳腺癌组织及癌旁组织各110例中的蛋白表达水平。在正常乳腺上皮细胞系MCF-10A和乳腺癌细胞系MCF-7中开展IQGAP1表达调控实验。结果:IQGAP1在乳腺癌组织中的表达高于癌旁正常乳腺组织(P=4.23×10^(-6))。IQGAP1的表达与浸润性导管癌的肿瘤大小(P=0.006)相关,在肿瘤>2 cm组明显高于肿瘤≤2 cm组。未发现与淋巴结转移(P=0.870),临床分期(P=0.278),ER状态(P=0.412)和PR状态(P=0.248)相关。IQGAP1高表达与乳腺癌术后无病生存时间(p=0.008)和总生存时间(P=0.029)相关。在乳腺癌细胞系MCF-7中,IQGAP1降低导致细胞增殖活性显著下降。结论:IQGAP1可能在乳腺癌的发生发展过程中发挥重要作用。
Objective: To investigate the expression of IQGAPI in breast cancer tissues and their tumor-adjacent normal tissues and the effect of IQGAP 1 on the proliferation of breast cancer cells. Methods: A total of 110 breast invasive ductal cancer ( IDC ) and its adjacent normal tissues specimens were screened for the expression of IQGAP1 with streptavidin-perosidase ( S-P ) immunohisto-chemistry. IQGAP1 gene expression was regulated in MCF-7 and MCF-10A cell line. Results: The expression of IQGAP1 was higher in breast cancer tissues than in tumor-adjacent normal tissues ( P = 4.23 x 10 6 ). The expression of 1QGAP1 was correlated with tumor size, and was significantly higher in tumor 〉 2 cm than in tumor ≤ 2 cm ( P = 0.006 ), but was not correlated with lymphnode metastasis ( P = 0.870 ), clinical staging ( P = 0.278 ), expression of estrogen receptor ( ER ) ( P = 0.412 ) or progestogen receptor (PR) ( P = 0.248 ) in IDC. IQGAP1 high expression was associated with poor progression free time ( P = 0.008 ) and overall survival time ( P = 0.029 ) among breast cancer patients. The proliferation rate of MCF-7 cells was significantly decreased after knocking down IQGAP1 expression, Conclusion: IQGAP 1 may play important roles in the development of breast cancer.
出处
《中国肿瘤临床》
CAS
CSCD
北大核心
2012年第9期555-558,共4页
Chinese Journal of Clinical Oncology
基金
国家自然科学基金面上项目(编号:30872172)
天津市科委中瑞合作项目(编号:09ZCZDSF04700)
天津市科委国际合作项目(编号:08ZCGHHZ02000)
教育部长江学者和创新团队发展计划(编号:lRTl076)资助~~
关键词
IQGAP1基因
乳腺癌
癌旁组织
免疫组化
细胞增殖
IQGAP1 gene
Breast cancer
Tumor-adjacent normal tissue
Immunohistochemistry
Cell proliferation