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吉非替尼联合顺铂对肺癌细胞增殖的协同抑制作用 被引量:1

Synergistic effect of gefitinib and cisplatin on proliferation of lung cancer cell line
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摘要 目的:观察表皮生长因子受体酪氨酸激酶抑制剂吉非替尼(Gefitinib,G)与顺铂(Cisplatin,DDP)联合对肺癌细胞株A549增殖抑制的协同效应。方法:采用四甲基偶氮唑蓝(MTT)法检测不同浓度吉非替尼单药、顺铂单药以及两药联用对肺癌细胞株A549的抑制程度,并应用两药相互作用指数评价药物的联合效应。结果:在药物作用时间足够时,两药联用相对单药组能显著地提高肿瘤细胞的抑制率,并且抑制效率随药物浓度的增加而提高。当作用时间≥48h时,联用组A值相对于单药组明显降低(P<0.05)。联用对肿瘤细胞增长的抑制作用在48h时较24h明显增高(P<0.05),并随着时间的延长呈现递增趋势,至72h后逐渐进入平台期(P>0.05)。两药协同效应在作用24h时表现不明显,在48h后才开始出现(CDI<1)。结论:在药物作用时间足够时,吉非替尼与顺铂联用对肺癌细胞的增殖具有协同抑制效应,可为临床应用提供参考。 Objevtive:To evaluate the synergistic effect of gefitinib and cisplatin on inhibition of proliferation of lung cancer cell line A549. Methods:The effect of gefitinib, cisplatin, and gefitinib in combination with cisplatin on lung cancer cell line A549 were detected by MTT assay, and the synergistic effect was analysed by the coefficient of drug interaction. Results:After 48h treatment, the combination of gefitinib and cisplatin inhibited the proliferation of A549 cells in a time - and dose - dependent manner. Conclusion: The single agent of gefitinib and cisplatin can inhibit the proliferation of A549 cells, and they have obvious synergistic activity. The combined EGFR - targeting thera py on lung cancer is worth of further exploration.
出处 《现代肿瘤医学》 CAS 2009年第11期2036-2039,共4页 Journal of Modern Oncology
基金 国家自然科学基金资助项目(编号:30600744)
关键词 吉非替尼 顺铂 肺癌细胞 增殖 gefitinib cisplatin lung cancer cell proliferation
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  • 1庄莉.吉非替尼对EGFR基因突变型晚期肺癌患者的影响[J].山东医药,2009,49(5):25-27. 被引量:2
  • 2牛怀印,穆海玉,王岩.肺癌分子靶向治疗进展[J].现代肿瘤医学,2008,16(12):2236-2239. 被引量:6
  • 3Degui Wang, Zhiping Wang, Binqiang Tian, et al. Two hour exposure to sodium butyrate sensitizes bladder cancer to antieaneer drugs [J]. Int J Urol,2008,15 (5) :435 -441.
  • 4雷亚丽,李代强.非小细胞肺癌表皮生长因子受体及其靶向治疗研究进展[J].国际病理科学与临床杂志,2009,29(1):59-63. 被引量:12
  • 5K Bencardino, M Manzoni, S Delfanti, et al. Epidermal growth factor receptor tyrosine kinase inhibitors for the treatment of non - small -cell lung cancer: results and open issues [ J]. Intern Emerg Med,2007,2( 1 ) :3 - 12.
  • 6Mendelsohn J, Baselga J. Status of epidermal growth factor receptor antagonists in the biology and treatment of cancer [J]. J Clin Oncol ,2003,21 (14) :2787 - 2799.
  • 7Srinivas Papaiahgari, Adinarayana Yerrapureddy, Paul M Hassoun, et al. EGFR - activated signaling and actin remodeling regulate cyclic stretch- induced NRF2 -ARE activation [ J]. Am J Respiratory Cell and Mol Biol,2007,36 (3) :304 -312.
  • 8Robert Mandic, Chantal J Rodgarkia - dara, Vanessa Krohn, et al. Cisplatin resistance of the HNSCC cell line UT - SCC - 26A can be overcome by stimulation of the EGF - Receptor [J].Anticaneer Res,2009,29:1181 - 1188.
  • 9Tiziana Servidei, Anna Riccardi, Simona Mozzetti, et al. Chemoresistant tumor cell lines display altered epidermal growth factor receptor and HER3 signaling and enhanced sensitivity to gefitinib [ J]. Int J Cancer,2008,123:2939 - 2949.
  • 10I-Iideyo Kurodaa, Mitsuhiro Takenoa, Shuji Murakamia, et al. Inhibition of heme oxygenase - 1 with an epidermal growth factor receptor inhibitor and cisplatin decreases proliferation of lung cancer A549 cells [J].Lung Cancer,2009,4 : 16.

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