摘要
目的:探讨IRESSA以不同次序联合化疗药(奈达铂、多西他赛和酒石酸长春瑞滨)对肺腺癌细胞系GLC-82 COX-2表达的不同作用。方法:流式细胞仪检测IRESSA不同次序联合化疗药奈达铂、多西他赛和酒石酸长春瑞滨时,GLC-82细胞表面COX-2表达情况,RT-PCR法检测COX-2的mRNA表达水平,Western blot检测COX-2蛋白的表达水平。结果:在化疗药之后使用IRESSA,将使GLC-82细胞有较低的COX-2表达率(酒石酸长春瑞滨为23.57%,奈达铂为12.1%,多西他赛为10.12%,P<0.05)、较低的COX-2 mRNA水平(酒石酸长春瑞滨为0.872±0.245,F=28.925,P=0.000;奈达铂为0.362±0.051,F=7.61,P=0.005;多西他赛为0.387±0.041,F=8.064,P=0.003)及较高的COX-2蛋白表达(酒石酸长春瑞滨为0.432±0.062,F=24.928,P=0.000;奈达铂为0.294±0.031,F=150.928,P=0.000;多西他赛为0.061±0.011,F=373.647,P=0.000)。结论:IRESSA和化疗药联合存在最佳方案,后用IRESSA效果优于先用IRESSA。
OBJECTIVE:To investigate the COX 2 contributions of gefitinib eombinated with chemotherapy drug (nedaplatin, docetaxel, vinorelbine) by diverse sequence on lung ear cinoma cell line GLC-82. METHODS:The GLC-82 cell COX-2 expression of nedaplatin, doeetaxel, and vinoreIbine combined with gefitinib of different sequences was measured by flow cytometry, COX-2 mRNA of the different combinations was detected by RT-PCR and COX-2 protein was analysed by Western blot. RESULTS: Applying gefitinib earlier or simultaneous created higher COX-2 expression (vinorelbine: 23.57 %; nedaplatin 12. 1%; docetaxel: 10. 12%. P〈0.05), mRNA level (vinorelbine: 0.872±0.245,F 28. 925 , P = 0. 000; nedaplatin 0.362±0.051, F= 7.61, P = 0.005; docetaxel: 0.387 ±0.041, F=8. 064, P= 0. 003 ) and more COX-2 protein (vinorelbine: 0. 432±0. 062, F= 24. 928, P = 0. 000; nedaplatin 0.294±0.031, F =150. 928, P =0. 000 ; docetaxel: 0.061±0.011,F 373.647,P=0.000). CONCLUSION: It is necessary to explore optimal schedule when gefitinib combined with chemotherapy drugs, to use gefitinib after chemotherapy drugs creats better curative effect than that before chemotherapy drugs.
出处
《中华肿瘤防治杂志》
CAS
2007年第5期345-348,共4页
Chinese Journal of Cancer Prevention and Treatment
关键词
肺肿瘤
抗肿瘤联合化疗方案
紫杉烷类
lung neoplasms
antineoplastic combined chemotherapy protocols
taxoids