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作 者:邓婷婷[1,2] 谢妮[3] 黄艳华[2] 黄海燕[2] 李子刚[4] 胡章立[1] 袁建辉[1,2]
机构地区:[1]深圳大学生命科学学院,广东深圳518060 [2]深圳市疾病预防控制中心,广东深圳518055 [3]深圳大学第一附属医院深圳市第二人民医院,广东深圳518035 [4]北京大学深圳研究生院,广东深圳518055
出 处:《癌变.畸变.突变》2014年第2期108-112,共5页Carcinogenesis,Teratogenesis & Mutagenesis
基 金:国家自然科学基金(30500599);广东省自然科学基金(915150310 2000019);深圳市科技计划重点项目(201201028);深圳市科技研发资金项目(JCYJ20120615085512920;JCYJ20120613171430264;ZYC201006180477A);深圳市孔雀计划(KQTD201103)
摘 要:目的:建立对米托蒽醌(Mit)耐药的乳腺癌MCF-7细胞系,并探讨乳腺癌细胞产生耐药与其基因组甲基化水平之间的关系。方法:用0.005、0.010和0.020μmol/L浓度的米托蒽醌染毒乳腺癌MCF-7细胞,建立对米托蒽醌不同耐药程度的MCF-7耐药细胞系,采用流式细胞术检测各染毒组MCF-7细胞内药物荧光强度D(755)值,确定Mit耐药细胞系的建立;提取各组细胞的DNA,利用毛细管电泳法检测野生型对照组及各染毒组细胞全基因组DNA甲基化水平。结果:野生型对照组、0.005、0.010和0.020μmol/L米托蒽醌染毒组的(755)值依次为16.1±0.04、14.3±0.12、13.3±0.07和9.7±0.08,与野生型对照组相比,随着药物染毒浓度的增加,MCF-7细胞内药物的D(755)值逐渐减少,其中0.020μmol/L染毒组较对照组显著减少,差异有统计学意义(P<0.05),表明细胞耐药性增强;而上述各组DNA甲基化水平依次为42.25%±0.64%、37.97%±1.18%、34.27%±0.14%、31.16%±0.80%,与野生型对照组相比,各染毒组细胞基因组DNA甲基化水平逐渐降低(P<0.05),且各染毒组间两两比较差异均具有统计学意义(P均<0.05)。结论:成功建立了对Mit耐药的MCF-7细胞系;确定了毛细管电泳法检测基因组DNA甲基化水平的电泳分离条件。【ABSTRACT】 OBJECTIVE: To establish a mitoxantrone-resistant MCF-7 breast cancer cell line,and toexplore the relationship between breast cancer cells developing drug resistance and their genomic methylation levels.METHODS:Using cells infected with 0,0.005,0.010 and 0.020 μmol/L mitoxantrone,different levels of drugresistance of MCF-7/Mit cell line was established. Flow cytometer was used to detect the accumulation of mitoxantrone inMCF-7 cells to confirm drug resistant cell lines. Then,we used capillary electrophoresis to evaluate genomic DNAmethylation levels of wide type and cells with different degrees of resistance. RESULTS:Compared with the controlgroup,with increasing mitoxantrone concentration,drug accumulation gradually decreased in MCF-7 cells. In the wildtypecontrol group,0.005,0.010 and 0.020 μmol/L -treated groups the drug D(755) values were 16.1±0.04, 14.3±0.12,13.3±0.07 and 9.7±0.08,respectively. The 0.02 μmol/L exposure group was significantly reduced comparedwith the control group,indicating that drug resistance was significantly increased (P〈0.05). In the wild-type controlgroup,0.005,0.010 and 0.020 μmol/L -treated groups,the DNA methylation levels were 42.25%± 0.64%,37.97%±1.18%,34.27%±0.14% and 31.16%±0.80%, respectively. Compared with the control group, genomic DNAmethylation levels in each group of treated cells gradually decreased (P〈0.05),with significant differences between eachtwo groups (P〈0.05). CONCLUSION:Mit drug-resistant MCF-7 cell line was successfully set up. The separationcondition of capillary electrophoresis when measuring genomic DNA methylation levels was determined.
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