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雌激素与贝伐单抗等因子对SKBR-3乳腺癌细胞VEGF表达影响观察
引用本文:郑斌,刘华,赵德重,刘若冰.雌激素与贝伐单抗等因子对SKBR-3乳腺癌细胞VEGF表达影响观察[J].齐鲁肿瘤杂志,2014(12):909-913.
作者姓名:郑斌  刘华  赵德重  刘若冰
作者单位:[1]昆明医科大学附属延安医院乳腺科,云南昆明650051 [2]昆明医科大学第一附属医院检验科,云南昆明650018
基金项目:云南省自然基金面上项目(2009CD204)
摘    要:目的:观察不同浓度雌激素对SKBR-3乳腺癌细胞血管内皮生长因子(vascularendothelialgrowthfactor,VEGF)表达的影响,并探讨不同浓度雌激素作用条件下,贝伐单抗(VEGF单抗)、曲妥珠单抗(HER-2单抗)、紫杉醇和胰岛素样生长因子1受体(insulin-likegrowthfactorreceptor,IGF-1R)抗体对SKBR-3乳腺癌细胞VEGF表达的影响。方法:利用RT-PCR方法检测SKBR-3乳腺癌细胞在不同浓度雌激素以及VEGF单抗(0.5μg/mL)、HER-2单抗(0.04μg/mL)、紫杉醇(1.5μg/mL)和IGF-1R抗体(2.5μg/mL)作用下,SKBR-3乳腺癌细胞VEGF的表达状况,利用ELISA方法检测培养液上清中VEGF蛋白浓度。结果:1)无雌激素组SKBR-3乳腺癌细胞VEGF表达为1.0618±0.0085(vEGF/GAPDH,下同),低浓度雌激素(0.05μg/mL,)组为1.0047±0.0061,差异有统计学意义,P=0.002,高浓度雌激素(O.2μg/mL)组为1.0868±0.0135,差异有统计学意义,P〈0.001。2)用与不用紫杉醇SKBR-3乳腺癌细胞VEGF表达分别为1.0496±0.0288和1.0618±0.0085,F=0.058;用与不用IGF=1R单抗为1.0884±0.0036和1.06184-0.0085,F=0.073;用与不用HER-2单抗分别为0.9887±0.0037和1.0618±0.0085,F=0.075;同时,在应用紫杉醇、IGF1R单抗、HER-2单抗基础上加用雌激素VEGF表达不受影响。3)用与不用VEGF单抗SKBR-3乳腺癌细胞VEGF表达分别为1.0057±0.0043、1.0618±0.0085,差异有统计学意义,F=0.132,P=0.04;但雌激素与VEGF单抗对VEGF表达影响没有协同作用。结论:不同雌激素浓度对SKBR-3乳腺癌细胞VEGF表达影响明显;紫杉醇、IGF-1R单抗和HER-2单抗不影响SKBR3乳腺癌细胞VEGF表达,与雌激素也无协同作用;VEGF单抗升高VEGF表达,也与雌激素没有协同作用。

关 键 词:乳腺肿瘤  雌激素  贝伐单抗  血管内皮生长因子  胰岛素样生长因子1受体抗体  曲妥珠单抗

Influence of estrogen,Bevacizumab on VEGF expression of SKBR-3 breast cancer cells
Authors:ZHENG Bin  LIU Hua  ZHAO De zhong  LIURuo-bing
Institution:1. Department of Breast ,Yanan Hospital of Kunming Medical University ,Kunmin 650051 ,P. R. China 2. Department of Lab, First Affiliated Hospital of Kunming Medical University, Kunming 650018, P. R. China)
Abstract:OBJECTIVE: To investigate expression of VEGF of SKBR-3 breast cancer cells in different estrogen and to investigate the expression of VEGF after Bevacizumab,Trastuzumab,Taxol and IGF-1R antibody treatment in different estrogen. METHODS: We examined VEGF-expression of the SKBR-3 breast cancer cells aftel: different cancentration of estrogen, Arastin, H erceptin, Taxoland IGF-1R antibody with RT-PCR. VEGF protein in supernate was detected by ELE- SA. RESULTS: The expression of VEGF in conto group was 1. 061 80. 008 5 (VEGF/GAPDH) ,the expression of VEGF in low concentration group(50 μg/L) was 1. 004 7 ± 0. 006 1 (P= 0. 002), the expression of VEGF in high concentration group (0.2 μg/mL) was 1. 086 8-1-0. 013 5(P〈0. 001). The expression of VEGF were 1. 049 6±0. 028 8 and 1. 061 8±0. 008 5 in Taxol group and contral group(F= 0. 058) ,the expression of VEGF were 1. 088 4 ± 0. 003 6,1. 061 8 ± 0. 008 5 in antibody of IGF-1R group and contral group( F= 0. 073), the expression of VEGF were 0. 988 7 ± 0. 003 7,1. 061 8 ± 0. 008 5 in Trastuzumab group and contral group(F=0. 075). There were no change of VEGF expression in Taxol group, antibody of IGF1R group and Trastuzumab group with estrogen. The expression of VEGF were 1. 005 7±0. 004 3 and 1. 061 8±0. 008 5 in Bevacizumab group and eontral group(F=0. 132, P= 0. 004) and estrogen had no influence on the action. CONCLUSIONS: The influence of different estrogen on VEGF expression in SKBR-3 breast cancer cells is remarkable. Taxol, antibody of IGF-1R and Trastuzumab do not change the expression of VEGF in SKBR-3 breast cancer cells and estrogen had no influence to this action. Bevacizumab increases the expression of VEGF and estrogen do not change the action.
Keywords:breast neoplasms  estrogen  bevacizumab  vascular endothelial growth factor  antibody of insulin likegrowth factor receptor  trastuzumab
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