Gu Wei-Guang, Huang Yan, Yuan Zhong-Yu, Peng Rou-Jun, Luo Hai-Tao, He Zhi-Ren, Wang Shu-Sen
Department of Medical Oncology, Sun Yat-Sen University Cancer Center, Guangzhou, China.
Asian Pac J Cancer Prev. 2013;14(3):1787-90. doi: 10.7314/apjcp.2013.14.3.1787.
This study evaluated the effects of ZD1839, an orally active, selective epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor, on nasopharyngeal carcinoma (NPC) both in vitro and in vivo. Influence of ZD1839 alone or combined with cisplatin on the NPC cell line CNE2 was detected by MTT assay with flow cytometry assessment of cell cycle distribution and apoptosis rates. Nude mice NPC xenografts were also used to evaluate the effects of ZD1839 alone or combined with cisplatin. The Student's t test evaluated statistical significance. ZD1839 alone or combined with cisplatin inhibited CNE2 cell line proliferation. ZD1839 induced CNE2 cell cycle arrest in the G1 phase, and higher concentrations induced apoptosis. Xenograft tumors were significantly smaller when treated with 200 mg/kg ZD1839, cisplatin, or cisplatin combined with 100 mg/kg ZD1839 than untreated controls. ZD1839 (200 mg/kg) alone showed good tumor inhibition effects, reduction of tumor weights, and smaller tumor volume without loss of body weight. ZD1839 (200 mg/kg) might provide a good and effective therapeutic reagent for NPC.
本研究评估了口服活性、选择性表皮生长因子受体(EGFR)酪氨酸激酶抑制剂ZD1839对鼻咽癌(NPC)的体内外作用。通过MTT法检测ZD1839单独或与顺铂联合对NPC细胞系CNE2的影响,并采用流式细胞术评估细胞周期分布和凋亡率。还利用裸鼠NPC异种移植模型评估ZD1839单独或与顺铂联合的作用。采用Student's t检验评估统计学意义。ZD1839单独或与顺铂联合均抑制CNE2细胞系增殖。ZD1839诱导CNE2细胞周期阻滞于G1期,较高浓度时诱导凋亡。与未治疗的对照组相比,用200 mg/kg ZD1839、顺铂或顺铂联合100 mg/kg ZD1839治疗时,异种移植瘤明显更小。单独使用ZD1839(200 mg/kg)显示出良好的肿瘤抑制作用,可减轻肿瘤重量、减小肿瘤体积,且不伴有体重减轻。ZD1839(200 mg/kg)可能为NPC提供一种良好且有效的治疗药物。