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反义ATM在体外对喉鳞状细胞癌ATM蛋白表达影响的研究 被引量:3

Study on the Protein Expression of Laryngeal Squamous Cell Carcinoma ATM by ATM Antisense Oligodeoxynucleotides in Vitro
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摘要 目的:用ATM反义多核苷酸作用于喉鳞状细胞癌以研究其对ATM蛋白表达的影响,进而推测其对放射治疗的敏感性。方法:用Western blot对AS、Sen、Misl、ipo与hep-2组的ATM蛋白进行分析。结果:AS、Sen、Misl、ipo与hep-2组(对照组)的ATM蛋白相对表达量以AS-lipo组最低,为48.14±5.53%,AS组与Sen、Misl、ipo、hep-2组比较有显著性差异。结论:ATM反义多核苷酸降低了喉鳞状细胞癌细胞中ATM蛋白的表达,其可能使喉鳞状细胞癌细胞对放射治疗的敏感性增强。 Objective:We used antisense oligodeoxynucleotides(AS-ODNs) to hep2(Human epidermoid laryngeal carcinoma) cells to study protein expression of ATM,and to analyze the sensitivity of hep-2 cells to radiation in vitro.Methods: In groups of AS、Sen、Mis、lipo and hep-2,the expression of ATM protein were examined by western blotting respectively.Results: The relative ATM protein expression in hep-2 cells treated with ATM AS-ODNs were decreased to 48.14±5.53% of that in untreated cells respectively(p0.05).There are no significant differences among liposome-treated group(Lipo),Sen-ODNs(Sen-Lipo) treated group and Mis-ODNs(Mis-Lipo) treated group(p0.05),while the group treated with ATM AS-ODNs notably different compared with other groups(p0.05).Conclusion: AS-ODNs of ATM canreduce ATM expression and may enhance hep-2 cells sensitive to radiation in vitro.
出处 《川北医学院学报》 CAS 2011年第5期394-396,共3页 Journal of North Sichuan Medical College
基金 国家自然科学基金(30872850) 四川省教育厅自然科学项目基金资助(2003A069)
关键词 ATM 反义ATM 喉鳞状细胞癌 ATM ATM Antisense oligodeoxynucleotides Squamous cell carcinoma
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参考文献7

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同被引文献22

  • 1Lei L, Michael S, Randy JL. Cellular responses to ionizing radiation damage [ J ]. Int J Radiat Oncol Biol Phys, 2001,49 ( 4 ) : 1157 - 1162.
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  • 7Zou J, Qiao XM,Ye HP, et al. Antisense inhibition of ATM gene enhances the radiosensitivity of head and neck squamous cell car- cinoma in mice [ J ]. Journal of Experimental & Clinical Cancer Re- search ,2008,27:56.
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  • 10Lin CS, Wang YC, Huang JL, et al. Autophagy and reactive oxy- gen species modulate cytotoxicity induced by suppression of ATM kinase activity in head and neck cancer cells [ J ]. Oral Oncol, 2012,48 ( 11 ) : 1152 - 1158.

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