期刊文献+

三氧化二砷对慢性髓系白血病细胞Hedgehog通路的影响 被引量:7

Effect of As_2O_3 on Hedgehog Pathway in Chronic Myeloid Leukemia Cells
下载PDF
导出
摘要 目的:探讨三氧化二砷对慢性髓系白血病(CML)细胞Hedgehog信号通路的影响。方法:采用MTT法及流式细胞术测定细胞的凋亡,Western blot检测Hedgehog通路中PTCH及SMO蛋白表达,real-time PCR检测PTCH及SMO基因mRNA的表达。结果:三氧化二砷可诱导K562细胞凋亡,最佳浓度为2μmol/L,最佳作用时间为24 h。在该浓度及时间点作用下Hedgehog通路中PTCH及SMO蛋白和mRNA表达下调。结论:三氧化二砷可降低Hedgehog通路中PTCH及SMO基因表达。 Objective:To explore the effect of As_2O_3 on Hedgehog pathway in chronic myeloid leukemia(CML)cells.Methods:The apoptosis of K562 cells was detected by MTT method and flowcytometry;the expressions of PTCH and SMO protein and mRNA in Hedgehog pathway were determined by Western blot and real-time PCR,respectively.Retults:The As_2O_3 could induce the apoptosis of K562 cells with optimal concentration 2 μmol/L and optimal time 24 hours.The expressions of PTCH and SMO protein and mRNA in Hedgehog pathway of K562 cells treated with As_2O_3 at optimal concentration and optimal time were down-regulated.Conclusion:The As_2O_3 can downregulate the expression of PTCH and SMO in Hedgehog pathway.
出处 《中国实验血液学杂志》 CAS CSCD 北大核心 2015年第4期971-975,共5页 Journal of Experimental Hematology
关键词 慢性粒细胞白血病 三氧化二砷 HEDGEHOG信号通路 chronic myeloid leukemia As2O3 Hedgehog signaling pathway
  • 相关文献

参考文献11

  • 1P.F. Seke Etet,L. Vecchio,A.H. Nwabo Kamdje.Signaling pathways in chronic myeloid leukemia and leukemic stem cell maintenance: Key role of stromal microenvironment[J]. Cellular Signalling . 2012 (9)
  • 2Beauchamp, Elspeth M,Ringer, Lymor,Bulut, Gülay,Sajwan, Kamal P,Hall, Michael D,Lee, Yi-Chien,Peaceman, Daniel,?zdemirli, Metin,Rodriguez, Olga,Macdonald, Tobey J,Albanese, Chris,Toretsky, Jeffrey A,üren, Aykut.Arsenic trioxide inhibits human cancer cell growth and tumor development in mice by blocking Hedgehog/GLI pathway[J]. Journal of Clinical Investigation . 2011 (1)
  • 3Christine Dierks,Ronak Beigi,Gui-Rong Guo,Katja Zirlik,Mario R. Stegert,Paul Manley,Christopher Trussell,Annette Schmitt-Graeff,Klemens Landwerlin,Hendrik Veelken,Markus Warmuth.Expansion of Bcr-Abl-Positive Leukemic Stem Cells Is Dependent on Hedgehog Pathway Activation[J]. Cancer Cell . 2008 (3)
  • 4Ellen Weisberg,Paul W. Manley,Werner Breitenstein,Josef Brüggen,Sandra W. Cowan-Jacob,Arghya Ray,Brian Huntly,Doriano Fabbro,Gabriele Fendrich,Elizabeth Hall-Meyers,Andrew L. Kung,Jürgen Mestan,George Q. Daley,Linda Callahan,Laurie Catley,Cara Cavazza,Azam Mohammed,Donna Neuberg,Renee D. Wright,D. Gary Gilliland,James D. Griffin.Characterization of AMN107, a selective inhibitor of native and mutant Bcr-Abl[J]. Cancer Cell . 2005 (2)
  • 5Nwabo Kamdje Armel Hervé,Mosna Federico,Bifari Francesco,Lisi Veronica,Bassi Giulio,Malpeli Giorgio,Ricciardi Mario,Perbellini Omar,Scupoli Maria Teresa,Pizzolo Giovanni,Krampera Mauro.Notch-3 and Notch-4 signaling rescue from apoptosis human B-ALL cells in contact with human bone marrow-derived mesenchymal stromal cells. Blood . 2011
  • 6C Zhao,A Chen,CH Jamieson,M Fereshteh,A Abrahamsson,J Blum,HY Kwon,J Kim,JP Chute,D Rizzieri,M Munchhof,T VanArsdale,PA Beachy,T Reya.Hedgehog signalling is essential for maintenance of cancer stem cells in myeloid leukaemia. Nature . 2009
  • 7Radoja S,Frey AB.Cancer-induced defective cytotoxic T lymphocyte effector function: another mechanism how antigenic tumors escape immune-mediated killing. Molecular Medicine . 2000
  • 8Lin Tara L,Wang Qiuju H,Brown Patrick,Peacock Craig,Merchant Akil A,Brennan Sarah,Jones Evan,McGovern Karen,Watkins D Neil,Sakamoto Kathleen M,Matsui William.Self-renewal of acute lymphocytic leukemia cells is limited by the Hedgehog pathway inhibitors cyclopamine and IPI-926. PloS one . 2011
  • 9Ito Keisuke,Bernardi Rosa,Morotti Alessandro,Matsuoka Sahoko,Saglio Giuseppe,Ikeda Yasuo,Rosenblatt Jacalyn,Avigan David E,Teruya-Feldstein Julie,Pandolfi Pier Paolo.PML targeting eradicates quiescent leukaemia-initiating cells. Nature . 2008
  • 10Yang D,Cao F,Ye X,et al.Arsenic trioxide inhibits the Hedgehog pathway which is aberrantly activated in acute promyelocytic leukemia. Acta Haematologica . 2013

共引文献2

同被引文献47

引证文献7

二级引证文献8

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