C225对人鼻咽癌细胞株CNE的生长抑制作用

徐寒子

徐寒子. C225对人鼻咽癌细胞株CNE的生长抑制作用[J]. 实用临床医药杂志, 2010, (7): 30-33. DOI: 10.3969/j.issn.1672-2353.2010.07.010
引用本文: 徐寒子. C225对人鼻咽癌细胞株CNE的生长抑制作用[J]. 实用临床医药杂志, 2010, (7): 30-33. DOI: 10.3969/j.issn.1672-2353.2010.07.010
XU Han-zi. Growth inhibition effect of C225 on human nasopharyngeal carcinoma CNE cell line[J]. Journal of Clinical Medicine in Practice, 2010, (7): 30-33. DOI: 10.3969/j.issn.1672-2353.2010.07.010
Citation: XU Han-zi. Growth inhibition effect of C225 on human nasopharyngeal carcinoma CNE cell line[J]. Journal of Clinical Medicine in Practice, 2010, (7): 30-33. DOI: 10.3969/j.issn.1672-2353.2010.07.010

C225对人鼻咽癌细胞株CNE的生长抑制作用

详细信息
  • 中图分类号: R739.63 R730.53

Growth inhibition effect of C225 on human nasopharyngeal carcinoma CNE cell line

  • 摘要: 目的 探讨EGFR单抗C225对人鼻咽癌细胞株CNE的生长抑制作用及可能机制.方法 以MTT比色法、倒置相差显微镜观察C225对CNE的生长抑制作用,以透射电镜、流式细胞术观察C225对CNE的凋亡诱导效应.结果 MTT法显示,C225对CNE具有明显的生长抑制作用,并随药物浓度的增加而逐渐增强,48 h IC20~30为10 μg/mL;以此浓度C225处理CNE,倒置相差显微镜观察发现,细胞变圆、脱壁,部分死亡、漂浮;透射电镜可见典型的凋亡超微结构改变;流式细胞术检测显示其24、48 h凋亡率分别为(14.30±0.78)%、(15.30±0.95)%,显著高于对照组的(2.90±0.95)%和(4.70±0.60)% (P<0.05).结论 C225对CNE细胞有明显的生长抑制作用,这可能其与诱导CNE凋亡有关.
  • Langer C J. Targeted therapy in head and neck cancer:state of the art 2007 and review of clinical applications [J]. Cancer, 2008, (12):2635.doi: 10.1002/cncr.23521.
    Zureikat A H, McKee M D. Targeted therapy for solid tumors:current status [J]. Surgical Oncology Clinics of North America, 2008(2):279.
    Ma B B, Poon T C, To K F. Prognostic significance of tumor angiogenesis, Ki 67, p53 oncoprotein, epidermal growth factor receptor and HER2 receptor protein expression in undifferentiated nasopharyngeal carcinoma--a prospective study [J]. Head & Neck, 2003, (10):864.
    Chua D T, Nicholls J M, Sham J S. Prognostic value of epidermal growth factor receptor expression in patients with advanced stage nasopharyngeal carcinoma treated with induction chemotherapy and radiotherapy [J]. International Journal of Radiation Oncology, Biology, Physics, 2004(1):11.doi: 10.1016/j.ijrobp.2003.10.038.
    Burgess A W. EGFR family:structure physiology signalling and therapeutic targets [J]. Growth Factors, 2008(5):263.
    Huether A, Hpfner M, Baradari V. EGFR blockade by cetuximab alone or as combination therapy for growth control of hepatocellular cancer [J]. Biochemical Pharmacology, 2005, (11):1568.doi: 10.1016/j.bcp.2005.09.007.
    Rivera F, Vega-Villegas M E, López-Brea MF. Cetuximab, its clinical use and future perspectives [J]. Anti-Cancer Drug Design, 2008(2):99.
    韦玮, 郭荣平, 李锦清. 西妥昔单抗联合厄洛替尼对人肝癌细胞的体外抑制作用 [J]. 癌症, 2008(4):386.doi: 10.3321/j.issn:1000-467X.2008.04.010.
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  • 发布日期:  2010-07-05

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