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溶瘤腺病毒介导IL-24增强黑素瘤细胞MV3放疗敏感性的研究
引用本文:孙超,;蒋冠,;魏志平,;郑骏年,;刘彦群.溶瘤腺病毒介导IL-24增强黑素瘤细胞MV3放疗敏感性的研究[J].中国麻风皮肤病杂志,2014(7):394-396.
作者姓名:孙超  ;蒋冠  ;魏志平  ;郑骏年  ;刘彦群
作者单位:[1]徐州医学院附属医院皮肤科,江苏徐州221002; [2]徐州医学院肿瘤生物治疗重点实验室,江苏徐州221002
基金项目:国家自然科学基金资助项目(编号:81372916,81141102)
摘    要:目的:研究溶瘤腺病毒介导IL-24(ZD55-IL-24)对黑素瘤细胞MV3放疗敏感性的影响。方法:将对数生长的MV3细胞分为ZD55-IL-24联合放疗组、ZD55-IL-24组、放疗组、PBS对照组。应用免疫细胞化学法检测黑素瘤MV3细胞中Bax和Bcl-2凋亡相关蛋白的表达:应用Western blot法检测E1A蛋白及Bax、Bcl-2、Caspase-3凋亡相关蛋白的表达。结果:免疫细胞化学法检测联合治疗组Bax染色强度最大,Bcl-2染色强度最小。ZD55-IL-24联合放疗作用的MV3细胞高效表达E1A,较其它组Bax的表达量增加,Bcl-2的表达量降低,Caspase-3活化更明显。结论:ZD55-IL-24联合放疗有明显的协同杀伤黑素瘤细胞的作用。

关 键 词:腺病毒科  放疗  黑素瘤  凋亡

Sensitivity to the melanoma cell line MV3 radiotherapy enhanced by oncolytic adenovirus mediated in terleukin-24
Institution:SUN Chao , JIANG Guan , WEI Zhi-ping , et al. (Department of Dermatology,Affiliated Hospital of Xuzhou Medical College, Xuzhou , 251002)
Abstract:To investigate the sensitivity to the melanoma cell line MV3 radiotherapy enhanced by oncolytic adenovirus mediated interleukin-24 (ZD55-IL-24). Methods: The logarithmic phase cells of melanoma cell line MV3 were divided into ZD55-IL-24 + radiotherapy group, ZD55-IL-24 group, radiotherapy group and PBS control group. Bax and Bcl-2 apoptosis related proteins of MV3 cells were measured by immunocytochemical staining. The expression of E1A proteins,Bax, Bcl-2 and Caspase-3 apoptosis related proteins were detected by Western blotting analysis. Results: The staining intensity of Bax was the strongest and the staining of Bcl-2 was weakest in ZD55-IL-24 plus radiotherapy group, when measured by immunocytochemical staining. Western blotting analysis showed that the expression of EIA was highest and the expression of Bax was also increased in ZD55-IL-24 plus radiotherapy group than other groups. The expression of Bcl-2 was decreased and the activation of Caspase-3 was more significant. Conclusion: ZD55-IL-24 conjugated with radiotherapy has a synergic effect in the killing of melanoma cells.
Keywords:adenoviridae  melanoma  radiotherapy  apoptosis
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