期刊文献+

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

Sensitivity to the melanoma cell line MV3 radiotherapy enhanced by oncolytic adenovirus mediated interleukin-24
下载PDF
导出
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。 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.
出处 《中国麻风皮肤病杂志》 2014年第7期394-396,共3页 China Journal of Leprosy and Skin Diseases
基金 国家自然科学基金资助项目(编号:81372916 81141102)
关键词 腺病毒科 放疗 黑素瘤 凋亡 adenoviridae melanoma radiotherapy apoptosis
  • 相关文献

参考文献2

二级参考文献11

  • 1Xin Yuan Liu~(1,2) ~1Institute of Biochemistry and Cell Biology,Shanghai Institutes for Biological Sciences,Chinese Academy of Sciences,320 Yue Yang Road,Shanghai 200031,China,~2Xinyuan Institute of Medicine and Biotechnology,School of Life Science,Zhejiang Sci-Tech University,Hangzhou 310018,China.Targeting Gene-Virotherapy of Cancer and its prosperity[J].Cell Research,2006,16(11):879-886. 被引量:32
  • 2Caudell EG, Mumm JB, Poindexter N, et al. The protein product of the tumor suppressor gene, melanoma differentiation-associated gene 7, exhibits immunostimulatory activeity and is designated Ⅱ.24. J Immunol, 2002,168:6041-6046.
  • 3Cunningham CC ,Chada S,Merritt JA,et al. Clinical and local biological effects of an intratumoral injection of mda-7 ( IL24 ;INGN 241 ) in patients with advanced carcinoma:a phase Ⅰ study. Mol Ther, 2005, 11 : 149-159.
  • 4Nishikawa T, Ramesh R, Munshi A, et al. Adenovirus-mediated mda-7 (IL24) gene therapy suppresses angiogenesis and sensitizes NSCLC xenograft tumors to radiation. Mol Ther,2004,9:818-828.
  • 5Cunningham CC, Chada S, Merritt JA, et al. Intratumoral injection of INGN 241, a nonreplicating adeno-vector expressing the melanoma-differentiation associated gene-7 (mda-7/IL24) :biologic outcome in advanced cancer patients. Mol Ther,2005,11 : 160-172.
  • 6Chada S, Mhashilkar AM, Ramesh R, et al. Bystander activity of Admda7 : human MDA27 protein kills melanoma cells via an IL-20 receptor-dependent but STAT32 independent mecha-nism. Mol Ther,2004, 10 : 1085-1095.
  • 7Kirn D. Oncolytic virotherapy for cancer with the adenovirus dll520 ( Onyx-015 ) : results of phase Ⅰ and Ⅱ trials. Expert Opin Biol Ther, 2001,1:525-538.
  • 8Melquist JJ, Kacka M, Li Y, et al. Conditionally replicating adenovirusmediated gene therapy in bladder cancer:An orthotopic in vivo model. Urologic Oncology,2005 ,24 :362-371.
  • 9Jacob D, Bahra M, humacher G. Gene therapy in colon cancer cells with a fiber- modified adenovector expressing the TRAIL gene driven by the hTERT promoter. Anticaneer Res 2004;24(5A) :3075 - 3079.
  • 10孙方浩,郑骏年,徐为,刘晓昀,张宝福,宋文哲,刘俊杰,章龙珍,顾玉明,高超,李望,裴冬生.Ki-67启动子的克隆及其转录活性[J].中华实验外科杂志,2009,26(1):87-88. 被引量:8

共引文献4

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部