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作 者:许诺[1] 姜军梅[1] 冯珊珊[1] 王冠华[1] 孟玫[1] 尹晓燕[1]
机构地区:[1]山东大学附属省立医院消化内科,济南250021
出 处:《山东大学学报(医学版)》2011年第8期48-51,共4页Journal of Shandong University:Health Sciences
基 金:山东省优秀青年科学家奖励基金资助项目(2000BB2DBA);山东省科技攻关基金资助项目(2005GG4402049)
摘 要:目的观察内源性一氧化氮(nitric ox ide,NO)对裸鼠肝癌模型中组蛋白去乙酰化酶4(histone deacety lase4,HDAC4)表达的影响,从而探讨新的抗肿瘤思路。方法免疫组化方法检测已经建立好的裸鼠肝癌模型中对照组、5-氟尿嘧啶组(5-FU)、5-氟尿嘧啶+L-精氨酸组(5-FU+L-A rg)诱导型一氧化氮合酶(inducib le nitric ox idesynthase,iNO S)与HDAC4的表达情况。结果 iNO S在对照组、5-FU组、5-FU+L-A rg组中表达呈平行递增关系,而HDAC4则表达为下降关系,每两组间比较差异均有统计学意义(P<0.05),iNO S和HDAC4在5-FU组、5-FU+L-A rg组的表达有显著相关性(P<0.05)。结论内源性NO下调HDAC4的表达,是HDAC功能作用的重要调节者,为抗肿瘤研究提供新的思路。Objective To investigate the effect of endogenous NO on expression of histone deacetylase 4 (HDAC4) in a hepatocellular carcinoma model of nude mice, and to explore a new antitumor idea. Methods Expressions of inducible nitric oxide synthase(iNOS) and HDAC4 were detected by immunohistochemistry in the control group, the 5-FU group and the 5-FU + L-Arg group in the established hepatocellular carcinoma model of nude mice. Results Expression of iNOS in the control group, the 5-FU group and the 5-FU + L-Arg group was increased, while expression of HDAC4 was depressed. Differences between the two groups were significant( P 〈 0.05 ). Expressions of iNOS and HDAC4 in the 5-FU group and 5-FU + L-Arg group had a significant correlation. ( P 〈 0.05 ). Conclusion Endogenous NO down-regulates expression of HDAC4, which is a key regulator of multiple HDAC functions. The relationship between endogenous NO and HDAC4 provides a new idea for antitumor study.
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