期刊文献+

替莫唑胺联合姜黄素对C6胶质瘤细胞凋亡的作用 被引量:10

Effect of temozolomide combined with curcumin on the apoptosis of the C6 glioma cells
在线阅读 下载PDF
导出
摘要 目的:研究替莫唑胺联合姜黄素用药对C6胶质瘤细胞的抑制作用和诱导凋亡作用。方法:SRB法考察替莫唑胺联合姜黄素对C6细胞的抑制作用;流式细胞法检测联合用药对C6细胞的凋亡作用;激光共聚焦扫描显微镜观察联合用药对细胞的诱导作用及在细胞中的定位作用。结果:SRB法结果显示替莫唑胺联合姜黄素在48 h时对C6细胞的抑制率为(91.22±0.51)%,显著高于24 h的抑制率(83.66±0.18)%(P<0.05);流式细胞仪检测结果表明,替莫唑胺(10μmol/L)联合姜黄素(5μmol/L)用药时C6细胞的早期凋亡率为(33.15±0.79)%;通过激光共聚焦扫描显微镜观察,姜黄素联合替莫唑胺组诱导C6细胞的凋亡细胞数量多于游离药物组。结论:替莫唑胺联合姜黄素用药能够抑制C6细胞的生长,同时可诱导C6细胞的凋亡。 Objective To study the temozolomide combined with curcumin on the inhibitory effect and apoptosis of the C6 glioma cells. Methods The C6 glioma cells were treated with temozomide in combination with curcumin. The anti proliferation effect of liposomes on the C6 glioma cells was investigated by using the method of sulforhodamine B(SRB). Flow cytometry was used to detect apoptosis of the C6 glioma cells. Confocal laser scanning microscope was used to observe apoptosis and location in the C6 glioma cells. Results The results of SRB assay showed that temozolomide in combination with curcumin inhibition rate were(91.22 ± 0.51)% in 48 h of the C6 glioma cells; Flow cytometry showed that the apoptosis rate were(33.15 ± 0.79)% with temozolomide(5 μmol / L)in combination with curcumin(10 μmol / L). Laser scanning confocal scanning microscope indicated that the apoptosis of in the C6 glioma cells treated with temozolomide in combination with curcumin was more than that of free drug. Conclusion The temozolomide in combination of curcumin can inhibit the growth and induce apoptosis of the C6 glioma cells.
出处 《实用医学杂志》 CAS 北大核心 2016年第10期1564-1567,共4页 The Journal of Practical Medicine
基金 国家自然科学基金项目(编号:81160396 81460540) 石河子大学杰出青年科技人才培育计划项目(编号:2012ZRKXJQ07) 新疆生产建设兵团社会发展科技攻关与成果转化计划项目(编号:2015AD007)
关键词 替莫唑胺 姜黄素 C6胶质瘤细胞 凋亡 抑制率 Temozolomide Curcumin C6 glioma cells Apoptisis Inhibition rate
作者简介 通信作者:应雪E—mail:yingxue2011@qq.com
  • 相关文献

参考文献13

  • 1SU X, CHEN HL, WANG ZY, et al. Relationship between tu- mour location and preoperative seizure incidence in patients with gliomas: a systematic review and meta-analysis [J]. Epileptic Disord, 2015,17(4) :397-408.
  • 2KARPEL-MASSLER G, B M, SHU, et al. TICI0/ONC201 synergizes with Bcl-2/Bcl-xL inhibition in glioblastoma by sup- pression of Mcl-1 and its binding partners in vitro and in vivo [ J ]. Oncotarget, 2015,6 ( 34 ) : 36456-36471.
  • 3CHEN L, LI X, LIU L, et al. Erastin sensitizes glioblastoma cells to temozolomide by restraining xCT and cystathionine-3,- lyase function [ J ]. Oncol Rep, 2015,33 ( 3 ) : 1465-1474.
  • 4TSO JL, SHUAI Y, MENJIVAR JC, et al. Bone morphogenetic protein 7 sensitizes O6-methylguanine methyltransferase express- ing-glioblastoma stem cells to clinically relevant dose of temo- zolomide [J]. nol Cancer, 2015,14( 1 ) : 1-17.
  • 5MCDONALD KL, TABONE T, NOWAK AK, et al. Somatic muta- tions in glioblastoma are associated with methylguanine-DNA methyltransferase methylation [ J ]. Oncol Lett, 2015,9 ( 5 ) : 2063- 2067.
  • 6WANG L, YE X, CAI X, el al. Curcumin suppresses cell growth and invasion and induces apoptosis by down-regulation of Skp2 pathway in glioma cells [J]. Oncotarget, 2015,6 (20) : 18027- 18037.
  • 7方大钊,王伟杰,董楠,付宪华,丁涟沭.STAT3反义核苷酸对脑胶质瘤U87细胞增殖、凋亡的影响及其作用机制[J].实用医学杂志,2013,29(23):3840-3843. 被引量:4
  • 8贺庆芝,曾怀才,于伟霞,李国庆,易岚.姜黄素致HepG-2细胞的凋亡作用及对bcl-2/bax表达的影响[J].实用医学杂志,2010,26(3):358-360. 被引量:14
  • 9ZANOTTO-FILHO A, BRAGANHOL E, KLAFKE K, et al. Au- tophagy inhibition improves the efficacy of curcumin/temozolo- mide combination therapy in glioblastomas [J]. Cancer Lett, 2015,358 (2) : 220-231.
  • 10陈欢欢,蔡炜嵩.替莫唑胺治疗多形性胶质母细胞瘤的化疗耐药机制[J].实用药物与临床,2015,18(2):215-219. 被引量:4

二级参考文献90

  • 1梁武,陈治军,罗勇,王凡.野生型p53基因可以增强胶质瘤细胞对替莫唑胺的敏感性研究[J].中华临床医师杂志(电子版),2011,5(13):3924-3926. 被引量:1
  • 2Shama R A, Gescher A J, Steward W P. Curcumin: the story so far [J]. Eur J Cancer, 2005,41 (13) : 1955-1968.
  • 3Lee Y K, Park S Y, Kim Y M, et al. Regulatory effect of the AMPK-COX-2 signaling pathway in curcumin-induced apoptosis in HT-29 colon cancer cells [J]. Ann N Y Acad Sci, 2009, 1171: 489-494.
  • 4Cory S, Huang D C, Adams J M. The Bcl-2 family:roles in cell survival and oncogenesis [J]. Oncogene, 2003, 22 (53): 8590- 8607.
  • 5Sukhotnik I, Voskoboinik K, Lurie M, et al. Involvement of the bax and bcl-2 system in the induction of germ cell apoptosis is correlated with the time of reperfusion after testicular isehemia in a rat model [J]. Fertil Steril, 2009, 92(4) : 1466-1469.
  • 6Matapurkar A, Lazebnik Y. Requirement of cytochrome c for apoptosis in human cells [J]. Cell Death Differ, 2006, 13 (12): 2062-2067.
  • 7Bomer C. The Bcl-2 protein family: sensors and checkpoints for lifeor-death decisions [J]. Mol Immunol, 2003, 39 (11 ) :615-647.
  • 8Rosse T, Olivier R, Monney L, et al. Bcl-2 prolongs cell survival after Bax-induced realease of cytochrome c [J]. Nature, 1998, 391 (6666) : 496-499.
  • 9Rong Y P, Bultynck G, Aromolaran A S, et al. The BH4 domain of Bcl-2 inhibits ER calcium release and apoptosis by binding the regulatory and coupling domain of the IP3 receptor [J]. Proc Natl Acad Sci USA, 2009, 106(34) : 14397-14402.
  • 10吴在德 吴肇汉.外科学[M]6版[M].北京:人民卫生出版社,2003.267-268.

共引文献39

同被引文献64

引证文献10

二级引证文献20

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