期刊文献+

羟基喜树碱联合热疗抑制人肝癌细胞SMMC-7721体外增殖作用的研究 被引量:10

THE RESEARCH ON THE COMBINATION OF HYDROXYCAMPTOTHECIN AND HYPERTHERMIA AGAINST HEPATOCELLULAR CARCINOMA CELL LINE SMMC-7721 IN VITRO
在线阅读 下载PDF
导出
摘要 目的探讨羟基喜树碱联合热疗体外抑制人肝癌细胞增殖的效果,以确定联合方案是否具有协同效应。方法使用MTT法测定单独或联合应用羟基喜树碱与热疗对人肝癌SMMC7721细胞的体外增殖的抑制作用,使用流式细胞仪检测不同方案对SMMC7721细胞凋亡率的影响。结果联合应用热疗可以显著提高羟基喜树碱引起的细胞增殖抑制及细胞凋亡。以亚毒性剂量浓度的羟基喜树碱为例,对照组、化疗组、热疗组、热化疗组的细胞增殖抑制率分别为0%、13.65%、32.46%、71.89%;细胞倍增时间分别为40.54、86.35、106.85、187.90h;细胞凋亡率分别为2.19%、3.96%、10.16%、20.42%。结论联合应用热疗与羟基喜树碱,对SMMC-7721细胞体外增殖的抑制及诱导细胞凋亡具有显著的协同作用。 Objectives To investigate whether concurrent exposure of human hepatocellular carcinoma cells SMMC-7721 to hydroxycamptothecine with hyperthermia will increase anticancer effects. Methods The MTT assay has been developed for quantitative evaluation of the proliferation of SMMC-7721 and cytotoxicity of hydroxycamptothecine with or without hyperthermia. Flow cytometric analyses were used for the assessment of apoptosis rates after treatment. Results The combined treatments significantly induced apoptosis and cytotoxicity higher than exposure to 43 ℃ hyperthermia alone or hydroxycamptothecin alone. Conclusion While both hyperthermia and hydroxycamptothecin can individually induce apoptosis and anti-proliferation effect, they may offer synergistic benefits when used concurrently.
出处 《实用临床医药杂志》 CAS 2005年第5期5-8,共4页 Journal of Clinical Medicine in Practice
基金 江苏省卫生厅重点资助项目(H200349)
关键词 热疗 羟基喜树碱 SMMC-7721细胞株 hyperthermia hydroxycamptothecine SMMC-7721
  • 相关文献

参考文献8

二级参考文献59

  • 1祝瑾,李宁川,程宏.TRAIL诱导白血病细胞凋亡的分子机制研究[J].实用临床医药杂志,2004,8(3):36-40. 被引量:8
  • 2李国栋.拓朴异构酶特性与肿瘤细胞的耐药性[J].河南肿瘤学杂志,1996,9(4):317-319. 被引量:72
  • 3Lilenbaum RC,Green MR. Novel chemotherapeutic agents in the treatment of non-small cell lung cancer[J]. J Clin Oncol, 1993,11:1391.
  • 4Katz EJ, Vick JS,Kling KM,et al. Effect of toikopoisomerase modulators on cisplatln cytotoxicity in human ovarian carcinoma cells[J]. Eur J Cancer, 1990,26:724.
  • 5van der Zee J. Heating the patient : a promising approach. Ann Oncol, 2002,13(8) : 1173-1184.
  • 6Takahashi I, Emi Y, Hasuda S, et al. Clincal application of hyperthernfia combined with anticancer drugs for the treatment of solid tumors. Surgery, 2002,131 (1 Suppl) : S78-S84.
  • 7Westermann AM, Grosen EA, Katschinski DM, et al. A pilot study of whole body hyperthermia and carboplatin in platinum-resistant ovarian cancer. Eur J Cancer, 2001, 37(9) : 1111-1117.
  • 8Rietbroek RC, van de Vaart PJ, Haveman J, et al. Hyperthermia enhances the cytotoxicity and platinum-DNA adduct formation of lobaplatin and oxaliplatin in cultured SW1573 cells. J Cancer Res Clin Oncol, 1997, 123(1): 6-12.
  • 9Hirohashi Y, Hidaka K, Sato S, et al. Biomodulation by hyperthermia of topoisomeraes II-targeting drug in human colorectal cancer cells. Jpn J Cancer Res, 1995, 86(11): 1097-1105.
  • 10Van Heek-Romanowski R, Putter S, Trarbach T, et al. Etoposide toxicity on human neuroblastoma cells in vitro is enhanced by preceeding hyperthermia. Med Pediatr Oncol,2001,36( 1 ) : 197-198.

共引文献132

同被引文献76

引证文献10

二级引证文献42

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