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作 者:王红芳[1] 宋爱琴[1] 孙立荣[1] 叶俊丽[2] 邢晓明[3] 杨堃[4] 张敏[1]
机构地区:[1]青岛大学附属医院血液儿科,山东青岛266003 [2]青岛大学医学院病理生理学教研室,山东青岛266021 [3]青岛大学附属医院病理科,山东青岛266003 [4]青岛大学附属医院中心实验室,山东青岛266003
出 处:《现代生物医学进展》2014年第12期2242-2246,共5页Progress in Modern Biomedicine
基 金:The Natural Science Foundation of China(31100824);The Natural Science Foundation of Shandong(Y2008c170);The Natural Science Foundation of Qingdao(2012-1-3-2-(5)-nsh)~~
摘 要:目的:探讨CHFR基因在B细胞淋巴瘤Raji细胞中的表达,以及CHFR基因甲基化对Raji细胞增殖和凋亡中所产生的影响。方法:体外培养人B细胞淋巴瘤细胞株Raji细胞,用不同浓度的去甲基化试剂5-氮杂-2脱氧胞苷处理Raji细胞株,通过RT-PCR检测CHFR基因表达水平的变化,通过MS-PCR检测CHFR基因甲基化变化,CCK法及流式细胞术检测Raji细胞增殖及凋亡变化。结果:CHFR基因在Raji细胞中出现弱表达,经去甲基化试剂处理后CHFR基因表达水平增高,随药物浓度增加Raji细胞的抑制率及凋亡率增高。结论:5-氮杂-2脱氧胞苷可以恢复CHFR基因表达水平,抑制Raji细胞的增殖,促进凋亡。CHFR基因在细胞增殖起负向调控的作用。Objective:To investigate mRNA expression level of CHFR gene in lymphoma cells,the effect of CHFR gene mathylation and methylation inhibition on Raji cells proliferation and apoptosis.Methods:The human Burkitt's Raji lymphoma cells were cultivated in vitro.Raji cells were treated in different concentration of methylation inhibitor 5- Aza-2'-deoxycytidine(5-Aza-dC),then the expression level change of CHFR gene was detected by RT-PCR and methylation of CHFR gene was analyzed by MS-PCR.The cells proliferation of Raji cells treated with different concentrations of 5-Aza-dC were analyzed by CCK assay.The apoptosis of Raji cells was analyzed by flow cytometry.Results:CHFR gene had low-expression in Raji cells.5-Aza-dC can up-regulate the expression of CHFR mRNA by demethylation.The growth of Raji cells was inhibited and the apoptosis was promoted by 5-Aza-dC.Conclusion:The expression of CHFR can be recovered by the methylation inhibition.CHFR gene can inhibit growth in Raji cells,and it may play a negative role during the growth and proliferation.
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