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阿糖胞苷与顺铂联用对耐药鼻咽癌细胞的生长抑制作用增强且细胞凋亡增加

Combination of cytosine arabinoside and cisplatin enhances inhibition of cell proliferation and promotes apoptosis of resistant nasopharyngeal carcinoma cells

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【作者】 陈建军刘世喜李启军彭杰

【Author】 CHEN Jianjun;LIU Shixi;LI Qijun;PENG Jie;Neijiang First People’s Hospital,Medical Department;ENT Department,West China Hospital,Sichuan University;

【机构】 内江市第一人民医院医务科四川大学华西医院耳鼻喉科

【摘要】 目的研究抗肿瘤药物阿糖胞苷(Ara-C)与顺铂(DDP)联用,或单独使用抗肿瘤药物,作用于具有顺铂耐药性的TW03/DDP鼻咽癌细胞,探讨细胞生长抑制和凋亡的差异及可能机制。方法体外培养TW03/DDP细胞,运用实时定量PCR和Western blot法检测细胞中肺耐药相关蛋白(LRP)的表达;Ara-C与DDP联用或单独使用处理TW03/DDP细胞和不具耐药性的TW03鼻咽癌细胞后,运用CCK-8法检测其生长抑制率,流式细胞术检测其凋亡率。结果相对于TW03细胞,TW03/DDP细胞中LRP蛋白表达升高;Ara-C与DDP单独使用均能抑制TW03/DDP细胞和TW03细胞的生长并诱导凋亡,但DDP对TW03/DDP细胞作用弱;Ara-C与DDP联用可抑制以上两种细胞的生长,抑制率和凋亡率均大于二者单独应用的效果。结论Ara-C与DDP联用可以增强对耐药性鼻咽癌细胞的生长抑制作用和凋亡诱导作用。

【Abstract】 Objective To investigate the synergistic cytotoxicity of cisplatin and cytosine arabinoside( Ara-C) on nasopharyngeal carcinoma( NPC) cell lines TW03 and cisplatin-resistant TW03/ DDP which is cisplatin-induced drug-resistant cell line. Methods The TW03/ DDP cells was established by gradually increasing the dose of cisplatin,and then examined by real-time quantitative PCR( qRT-PCR) and semi-quantitative Western blotting for the expression level of lung resistancerelated protein( LRP). Effects of DDP and Ara-C combined treatment or alone on proliferation and apoptosis of TW03/ DDP cells and TW03 cells were detected by CCK-8 assay and flow cytometry,respectively. Results Compared with TW03 cells,TW03/ DDP cells expressedhigher level of LRP. After treatments for 24hours,both cisplatin and Ara-C inhibited proliferation and caused apoptosis of TW03/ DDP and TW03 cells,and DDP showedminor effect on the proliferation of TW03/ DDP cells.Compared with Ara-C or DDP treatment alone,combination of Ara-C and DDP showed a more remarkable inhibition of proliferation and promotion of apoptosis in both TW03 and TW03/ DDP cells. Conclusion Ara-C and DDPhave a synergistic killing effect on NPC cell lines with and without DDP-caused drug resistance,and show better effects on proliferation inhibition and apoptosis promotion than Ara-C or DDP treatment alone,which provides a novel and prospective strategy for NPC chemotherapy.

【基金】 四川省科技厅科技支撑计划(2012SZZ011)
  • 【文献出处】 细胞与分子免疫学杂志 ,Chinese Journal of Cellular and Molecular Immunology , 编辑部邮箱 ,2015年03期
  • 【分类号】R739.63
  • 【被引频次】5
  • 【下载频次】101
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