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 |
本文献已被 维普 等数据库收录! |
|