检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:付洁[1] 刘曼[2] 宿颖[2] 张辛燕[2] FU fie LIU Man SU Ying ZHANG Xin-yan(Department of Oral Medicine, Capital Medical University School of Stomatology, Beijing 100050, China)
机构地区:[1]首都医科大学口腔医学院黏膜科,北京100050 [2]首都医科大学口腔医学研究所,北京100050
出 处:《北京口腔医学》2016年第5期241-245,共5页Beijing Journal of Stomatology
基 金:国家自然科学基金(81272982);北京市自然科学基金(7162073)
摘 要:目的探讨人口腔鳞癌中DNA甲基化和组蛋白乙酰化对KLF4基因的调控作用。方法体外培养人口腔鳞癌细胞系SCC-6,分别用DNA甲基化抑制剂5-氮-2’-脱氧胞苷(DAC)、组蛋白去乙酰化酶抑制剂曲古抑菌素A(TSA)处理SCC-6细胞,并据此将SCC-6分为4组,阴性对照组(不做处理)、DAC处理组、TSA处理组、DAC+TSA联合处理组,采用荧光定量PCR方法检测SCC-6细胞经DAC或/和TSA处理前后KLF4 RNA水平的变化;用免疫细胞化学方法检测SCC-6细胞经DAC或/和TSA处理前后KLF4蛋白的变化。结果 SCC-6细胞DAC处理组、TSA处理组、DAC+TSA组的KLF4 RNA水平与阴性对照组相比均有显著升高(P<0.01)。另外,DAC处理组KLF4 RNA水平均高于其他3组(P<0.01)。SCC-6细胞DAC处理组中KLF4蛋白表达明显升高,均高于其他3组(P<0.01)。TSA处理组与DAC+TSA联合组KLF4蛋白表达也都高于阴性对照组(P<0.01);TSA处理组与DAC+TSA处理组间无显著差异(P>0.05)。结论在口腔鳞状细胞癌SCC-6细胞中导致KLF4基因沉默的主要原因可能为DNA甲基化,此外组蛋白乙酰化可能也参与了KLF4表达的调控,但组蛋白乙酰化在提高KLF4表达方面与去甲基化无明显协同作用。Objective To investigate the regulation of DNA methylation and histone acetylation in oral squamous cell carcinoma(OSCC) cells on KLF4 gene. Methods SCC-6 ceils were divided into four groups, negative group (without any treatment), DAC group ( treated with DAC- DNA methylation inhibitor), TSA group (treated with TSA- histone deacetylase inhibitors) and DAC + TSA group( treated with DAC + TSA). Quantitative PCR was used to examine the RNA expression of KLF4 in SCC-6 before and after the treatment of DAC or/and TSA. Immuneeytochemistry was used to detect KLF4 protein expression before and after the treatment of DAC or / and TSA in SCC-6 cells. Results KLF4 RNA expression in DAC group, TSA group, and DAC + TSA group was significantly higher than that in the negative control ( P 〈 0.01 ). There was no significant difference between TSA group and DAC + TSA group ( P 〉 0.05 ). The KLF4 RNA expression in DAC group was higher than that in other three groups (P 〈0.01 ). The protein expression of KLF4 in DAC group was significantly higher than that in other three groups. (P 〈 0.01 ). KLF4 expression was not significantly different between the TSA group and DAC + TSA group (P 〉 0. 05 ), but was significantly higher in TSA and DAC + TSA groups than that in the negative control (P 〈0.01 ). Conclusion DNA methylation may be the main reason for KLF4 silence in SCC-6 ceils ,and histone acetylation may also participate in the regulation of KLF4 expression, but DNA methylation and histone acetylation has no synergistic effect on improving the expression of KLF4.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.222