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荷载白介素24的溶瘤腺病毒联合达卡巴嗪对裸鼠黑素瘤的抑制作用 被引量:1

Inhibitory effect of dacarbazine and an oncolytic adenovirus carrying interleukin.24 on transplanted melanoma in nude mice
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摘要 目的研究荷载白介素24(IL-24)的溶瘤腺病毒ZD55-IL-24联合达卡巴嗪抑制裸鼠黑素瘤的作用。方法建立裸鼠恶性黑素瘤A375细胞移植瘤模型后,分别给予ZD55-IL-24联合达卡巴嗪、ZD55-IL-24、达卡巴嗪、磷酸盐缓冲液(PBS)干预。Western印迹法检测A375细胞移植瘤组织IL-24、E1A蛋白表达。测量裸鼠肿瘤生长体积。结果Western印迹结果表明,ZD55-IL-24联合达卡巴嗪作用的裸鼠黑素瘤高效表达IL-24、E1A蛋白。接种30d后,ZD55-IL-24联合达卡巴嗪组肿瘤平均体积为(2346.5±576.0)mm3,ZD55-IL-24组为(4141.6±1348.2)mm3,达卡巴嗪组为(5230.1±922.8)mm3,PBS组为(7135.1±1002-3)mm3,ZD55-IL-24联合达卡巴嗪组与各组之间差异均有统计学意义(P〈0.05)。结论荷载IL-24基因的溶瘤腺病毒ZD55-IL-24联合达卡巴嗪有抑制黑素瘤增殖的作用。 Objective To investigate the inhibitory effect of dacarbazine and an oncolytic adenovirus carrying interlenkin-24 (IL-24) on transplanted melanoma in nude mice. Methods Nude mice were inoculated with human A375 melanoma cells to establish a model of malignant melanoma. Then, the mice were divided into 4 groups to be treated with an oncolytic adenovirus carrying interleukin-24 (ZD55-IL-24), dacarbazine, the combination of ZD55-IL-24 and dacarbazine, and phosphate buffer (PBS), respectively, for 3 days. Seven days after the end of the treatment, some mice were sacrificed followed by the determination of IL-24 and E1A protein levels in tumor tissue by Western blot. The tumor volume was measured on a daily basis for 30 days. Results IL-24 and EIA were highly expressed in melanoma cell-bearing nude mice treated with ZD55-IL=24 and dacarbazine. At 30 days after the inoculation, the average volume of transplanted melanoma was (2346.5 ± 576.0) mm3 in the combination group, significantly different from that in the ZD55-IL-24 group ((4141.6 ± 1348.2) mm3, P 〈 0.05), dacarbazine group ((5230.1± 922.8) mm3, P 〈 0.05), and the control group ((7135.1 ± 1002.3) mm3, P 〈 0.05). Conclusion The ZD55-IL-24 in combination with dacarbazine exhibits a remarkably inhibitory effect on the proliferation of melanoma transplanted into nude mice.
出处 《中华皮肤科杂志》 CAS CSCD 北大核心 2012年第4期282-283,共2页 Chinese Journal of Dermatology
基金 基金项目:国家自然科学基金(81141102) 徐州市科技发展基金(XF10C064)
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