辐射促进多药耐药反义寡脱氧核苷酸体内逆转耐药的实验研究The Ionic Radiation Promoted Improvement of Multidrug Resistance Reversal in vivo by mdr1 Antisense Oligodeoxynucletides
潘耀振,孙诚谊,王玉芝
PAN Yao-zhen; SUN Cheng-yi; WANG Yu-zhi
;
摘要(Abstract):
目的:探讨辐射促转染的多药耐药(MDR)基因mdr;反义寡核苷酸(ASON)体内逆转肿瘤耐药的效果。方法:采用耐药细胞株KBv_(200)移植于裸鼠皮下,建立肿瘤耐药模型,肿瘤局部2Gy~(60)Co-γ辐射后1h,瘤内注射脂质体介导的mdr_1 ASON,经长春新碱联合化疗。结果:对照组与联合辐射组、未联合辐射组肿瘤生长曲线差异有显著性(P<0.01),联合辐射组与未联合辐射组肿瘤生长曲线差异有显著性(P<0.01)。对照组与联合辐射组、未联合辐射组肿瘤体积和肿瘤重量差异有显著性(P<0.01),联合辐射组与未联合辐射组肿瘤体积和肿瘤重量差异有显著性(P<0.01)。联合辐射组肿瘤重量抑制率为(80.78±1.9)%,肿瘤体积抑制率为(84.91±2.1)%。结论:辐射促转染的mdr_1 ASON对肿瘤细胞具有较强的耐药逆转作用。
Objective:To investigate the reversal of tumor multidrug resistance (MDR) in vivo by MDR gene mdr, antisense oligodeoxynucletides (ASON) in combination with ionic radiation. Methods: A nude mice model transplanted with resistant cell line KBv200 was established. Mdr1 ASON was injected into tumor in 1 hour after local 2Gy 60Co-γ radiation. The tumor-suppressing rates and tumor-suppressing curves were observed in experimental groups and control group after treatment by vincrstine (VCR). Results: The results showed that the significant differences of tumor growth curves occurred between control group and treated groups (P < 0. 01) , and between treated groups that accepted combined radiation or not (P <0.01) . Significant differences of tumor weight and tumor volume were also observed between the two different treated groups (P <0. 01). The suppressing rates of tumor volume and weight were 84.91±2. 1% and 80.78±1.9% respectively in group accepted combined radiation. Conclusion: The reversal effect of mdr, ASON on the resistance cell line could be strengthened when combined with ionic radiation.
关键词(KeyWords):
辐射;电离;抗药性;多药;寡核苷酸类;反义;大鼠;裸
radiation, ionizing; drug resistance, multiple; oligodeoxynucletides, antisense; mice, nude
基金项目(Foundation): 贵州省科学技术基金资助项目(黔基合计字20023106)
作者(Authors):
潘耀振,孙诚谊,王玉芝
PAN Yao-zhen; SUN Cheng-yi; WANG Yu-zhi
;
DOI: 10.19367/j.cnki.1000-2707.2003.04.001
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文章评论(Comment):
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- 辐射
- 电离
- 抗药性
- 多药
- 寡核苷酸类
- 反义
- 大鼠
- 裸
radiation, ionizing - drug resistance, multiple
- oligodeoxynucletides, antisense
- mice, nude