期刊文献+

格列卫对K562细胞中miR-146a、miR-29b及3种甲基化酶表达的影响 被引量:1

Influence of Gleevec on expression of miR-146a,miR-29b and DNMT in K562 cells
下载PDF
导出
摘要 目的观察BCR/ABL抑制剂格列卫作用后K562细胞中microRNA(miR)-146a及miR-29b的表达水平变化及DNMT1、DNMT3a、DNMT3b3种甲基化酶水平的改变。方法 MTT法检测格列卫作用于K562细胞时的IC50浓度。通过茎环引物法及荧光定量PCR的方法检测miRNAs以及甲基化酶基因的水平。结果格列卫作用于K562细胞时的IC50浓度为40.85μmol/L。格列卫作用后miR-29b表达出现了上升的趋势而3种甲基化酶基因表达水平均有所降低,miR-146a的水平显著升高(P<0.05)。结论格列卫能影响K562细胞中miR-146a、miR-29b和3种甲基化酶的表达水平。 Objective To investigate the changes of microRNA (miR)-146a ,miR-29b expression levels and the 3 kinds of meth-ylase DNMT1 ,DNMT3a and DNMT3b levels in K562 cell lines after BCR/ABL inhibitor Gleevec treatment .Methods The half maximal inhibitory concentration(IC50 ) of Gleevec on K562 cells was detected by the MTT method .The stem loop primers method and the fluorogenic quantitative PCR were adopted to detect miRNAs and the methylase gene level .Results IC50 of Gleevec acting on K562 cells was 40 .85μmol/L .After Gleevec action ,miR-29b showed the increasing trend ,but 3 kinds of methylase expression level were decreased to some extent .Gleevec could significantly increase the miR-146a level in K562 cells(P&lt;0 .05) .Conclusion Gleevec can influence the expression of miR-146a ,miR-29b and DNMTs levels in K562 cells .
出处 《重庆医学》 CAS CSCD 北大核心 2014年第3期301-303,共3页 Chongqing medicine
基金 广东省自然科学基金资助项目(S2012010008916)
关键词 慢性粒细胞白血病 甲基化酶 格列卫 chronic MYELOGENOUS leukemia(CML) microRNA146a microRNA146a DNMT Gleevec
  • 相关文献

参考文献12

  • 1Kaufmann SH. Imatinib spells BAD news for Bcr/abl-positive leukemias[J].{H}Proceedings of the National Academy of Sciences(USA),2006,(40):14651-14652.
  • 2Taganov KD,Boldin MP,Chang KJ. NF-kappaB-IN-dependent induction of microRNA miR-146,an inhibitor targeted to signaling proteins of innate immune responses[J].{H}Proceedings of the National Academy of Sciences(USA),2006,(33):12481-12486.
  • 3Starczynowski DT,Morin R,McPherson A. Ge-nome-wide identification of human microRNAs located in leukemia-associated genomic alterations[J].{H}Blood,2011,(2):595-607.
  • 4赵斌,葛金芳,朱娟娟,黄晓晖,李俊.小议在MTT法测细胞增殖抑制率中IC_(50)的计算方法[J].安徽医药,2007,11(9):834-836. 被引量:167
  • 5Wang S,Zhang X,Ju Y. MicroRNA-146a feedback suppresses T cell immune function by targeting Stat 1 in patients with chronic hepatitis B[J].{H}Journal of Immunology,2013,(1):293-301.
  • 6Zhao JL,Rao DS,O′Connell RM. MicroRNA-146a acts as a guardian of the quality and longevity of hemato-poietic stem cells in mice[J].Elife,2013.e00537.
  • 7Yang L,Boldin MP,Yu Y. miR-146a controls the resolution of T cell responses in mice[J].{H}Journal of Experimental Medicine,2012,(9):1655-1670.
  • 8Nakamura S,Yokota D,Tan L. Down-regulation of Thanatos-associated protein 11 by BCR-ABL promotes CML cell proliferation through c-Myc expression[J].{H}International Journal of Cancer,2012,(5):1046-1059.
  • 9Flamant S,Ritchie W,Guilhot J. Micro-RNA re-sponse to imatinib mesylate in patients with chronic mye-loid leukemia[J].{H}HAEMATOLOGICA,2010,(8):1325-1333.
  • 10Wang Y,Li Z,He C. MicroRNAs expression signa-tures are associated with lineage and survival in acute leu-kemias[J].{H}Blood Cells Molecules and Diseases,2010,(3):191-197.

二级参考文献13

  • 1李保华,董向丽,孙显明,赵川德,才秀华,孙立宁.用于计算半数致死量(LD50)的SAS程序[J].莱阳农学院学报,2004,21(4):269-274. 被引量:10
  • 2司徒镇强 吴军正.细胞培养[M].西安:世界图书版出版公司,2004.78-202.
  • 3刘昌孝 孙瑞元.药物评价实验设计与统计学基础[M].北京:军事医学科学出版社,2001,4.84-88.
  • 4RI弗雷谢尼,动物细胞培养基本技术指南(分子克隆实验指南系列)[M].第4版.北京:科学出版社,2004:398-400.
  • 5Yam J,Reer PJ,Bruce RD.Comparison of the up-and-down method and the fixed-dose procedure for acute oral toxicity testing[M].Food Chem Toxicol.ENGLAND.1991:259-63.
  • 6Van den Heuvel MJ,Clark DG,Fielder RJ.et al.The international validation of a fixed-dose procedure as an alternative to the classical LD50 test[M1].Food Chem Toxicol.ENGLAND,1990:469-82.
  • 7Halle W.The Registry of Cytotoxicity:toxicity testing in cell cultures to predict acute toxicity(LD50)and to reduce testing in animals[M].Altern Lab Anim.England,2003:89-198.
  • 8Schlede E,Genschow E,Spielmann H,et al.Oral acute toxic class method:a successful alternative to the oral LD50 test[M].Regul Toxicol Pharmacol.United States,2005:15-23.
  • 9Mosmann T.Rapid colorimetric assay for cellulr growth and survival:application to proliferation and cytotoxicity assays[M].J Immunol Methods.NETHERLANDS.1983:55-63.
  • 10马桢红,马良才.生物测定中LC_(50)或LD_(50)的Excell运算方法[J].医学动物防制,1999,15(11):612-614. 被引量:11

共引文献166

同被引文献8

引证文献1

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