期刊文献+

氢醌对DNA甲基转移酶表达的影响 被引量:2

Effects of Hydroquinone on the Expression of DNA Methyltransferase
原文传递
导出
摘要 目的探索氢醌(hydroquinone,HQ)致DNA整体低甲基化的分子机制。方法以磷酸盐缓冲液(PBS)溶解HQ,以PBS处理组为对照组,分别以2.5、5.0、10.0和20.0μmo/lL HQ染毒TK6细胞为处理组。应用实时荧光定量-聚合酶链反应检测DNA甲基转移酶DNMT1、DNMT3a和DNMT3b的表达水平。结果与对照组相比,DNMT1、DNMT3a和DNMT3b的mRNA表达量在各HQ处理组细胞中均下降,其中以20.0μmo/lL组细胞的下降最为明显,分别下降46%(P<0.05)、83%(P<0.05)和48%(P<0.05),且DNMT1和DNMT3a的表达量随着HQ剂量的增加而下降。结论 HQ致DNA整体低甲基化下调机制可能与DNMT1、DNMT3a和DNMT3b表达异常有关。 Objective To explore the molecular mechanisms of global DNA hypomethylation induced by hydroquinone(HQ).Methods TK6 cells were exposed to 2.5,5.0,10.0 and 20.0 μmol/L HQ prepared by PBS buffer,and TK6 cells treated with PBS served as the control.Expressions of DNA methyltransferase(DNMT),DNMT1,DNMT3a and DNMT3b,were tested by real-time fluorescence quantitive PCR.Results Expressions of DNMT1,DNMT3a and DNMT3b mRNA in the HQ-treated cells were severely inhibited as compared to those in the control cells,with the most remarkable inhibition at 20 μmol/L,showing a decrease by 46%,83% and 48% respectively(all P0.05).The expressions of DNMT1 and DNMT3a showed more decrease with the increase of HQ dose.Conclusions Global DNA hypomethylation induced by hydroquinone may be associated with the deregulated expressions of DNMT1,DNMT3a and DNMT3b.
出处 《实用预防医学》 CAS 2012年第7期961-963,共3页 Practical Preventive Medicine
基金 国家自然科学基金(30972500) 广东省自然科学基金(7301507) 东莞市科技计划项目(201010815206)
关键词 氢醌 DNA甲基转移酶 基因表达 Hydroquinone DNA methyltransferase Gene expression
  • 相关文献

参考文献11

  • 1Bollati V, Bacearelli A, Hou L, et al. Changes in DNA methylation patterns in subjects exposed to low- dose benzene[J]. Cancer Res, 2007, 67 : 876 - 880.
  • 2Jagetia GC, Aruna R. Hydroquinone increases the frequency of micro- nuclei in a dose- dependent manner in mouse bone marrow[J]. Toxicol Lett, 1997, 93:205-213.
  • 3Ji Z, Zhang L, Peng V, et al. A comparison of the cytogenetic alter- ations and global DNA hypomethylation induced by the benzene metabo- lite, hydroquinone, with those induced by melphalan and etoposide[J ]. Leukemia, 2010, 24:986-891.
  • 4刘林华,凌晓璇,梁海荣,翟璐,唐焕文.氢醌诱导TK6细胞miR-221表达异常致PARP-1基因下调的机制[J].环境与健康杂志,2011,28(6):485-487. 被引量:9
  • 5刘林华,蒋义国,纪卫东,杨巧媛.结晶型硫化镍对人支气管上皮细胞PTEN基因和miR-22表达的影响[J].环境与健康杂志,2010,27(5):393-395. 被引量:7
  • 6Liu Q, Yang L, Gong C, et al. Effects of long- term low - dose form- aldehyde exposure on global genomic hypomethylation in 16HBE cells [ J ]. Toxieol Lett, 2011, 205 : 235 - 240.
  • 7Eden A, Gaudet F, Waghmare A, et al. Chmmosomed instability and tttmors promoted by DNA hypomethylation [ J ]. Science, 2003, 300: 455.
  • 8Ley TJ, bing L, Waiter MJ, et al eloid leukemia [J]. N Engl J Med, DNMT3A mutations in acute my 2010, 363:2424 - 2433.
  • 9Thol F, Damrn F, Ludeking A, et al. Incidence and prognostic influ- ence of DNMT3A mutations in acute myeloid leukernia[J ]. J Clin On- col, 2011, 29:2889-2896.
  • 10Gao Q, Steine EJ, Barrasa MI, et al. Deletion of the de novo DNA methyltransferase Dnmt3a promotes lung tumor progression [ J ]. Proc Natl Acad Sci USA, 2011, 108:18061 - 18066.

二级参考文献11

共引文献13

同被引文献13

引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部