摘要
目的在细胞和动物水平评价强心苷药物吉妥辛对耐药性非小细胞肺癌的抑制作用,并对其抑癌的分子机制进行初步探索。方法吉妥辛和吉非替尼处理H1975细胞后,用MTS法检测细胞的存活率,流式细胞分析法检测细胞的凋亡率;吉妥辛处理移植瘤裸鼠,测量并计算移植瘤体积;吉妥辛处理H1975细胞后,用Western blot检测Erk1/2的磷酸化水平。结果吉妥辛比吉非替尼更有效地抑制H1975的生长(P<0.05),促进其凋亡(P<0.05),且能显著抑制裸鼠移植瘤的生长(P<0.05)。吉妥辛能计量和时间依赖地抑制Erk1/2的磷酸化(P<0.05)。结论吉妥辛可作为治疗耐药性非小细胞肺癌的潜在替代药物。
Objective To evaluate the inhibitory effect of gitoxin on non small cell lung cancer with drug-resistance in vitro and in vivo and to explore the underlying molecular mechanism. Methods Survival and apoptosis rates of H1975 were measured by MTS assay and flow cytometry respectively after gitoxin and gefitinib treatments. Tumor volumes of gitoxin treated xenograft nude mice were calculated by measuring the lengths and widths of these tumors. The phosphorylation of Erkl/2 was analyzed by Western blot. Results Gitoxin inhibited the growth of H1975 and induced its apoptosis more effectively than gefitinib. It also inhibited growth of transplanted tumors in nude mice. In addition, gitoxin inhibited the phosphorylation of Erkl/2 in a dosage and time dependent way. toxin may offer a potential treatment for drug resistant NSCLC.
出处
《基础医学与临床》
CSCD
北大核心
2013年第5期609-613,共5页
Basic and Clinical Medicine