期刊文献+

金喜素诱导人肝癌HCC7721细胞凋亡及细胞周期阻滞的研究 被引量:2

Topotecan induces apoptosis and cell cycles arrest in human liver cancer HCC7721 cells
下载PDF
导出
摘要 目的 :研究金喜素诱导人肝癌HCC772 1细胞的凋亡作用。方法 :采用MTT法测定金喜素对人肝癌HCC772 1细胞的杀伤作用 ;通过电镜观察细胞形态变化 ;琼脂糖凝胶电泳检测断裂DNA ;流式细胞仪分析DNA含量及细胞周期。结果 :经0 3 μmol/L金喜素处理 6、12、2 4及 3 6h ,HCC772 1细胞的存活率与对照组相比 ,逐渐降至 ( 83± 16) %、( 69± 10 ) %、( 5 2±13 ) %和 ( 3 0± 11) % ,低于对照组 ,P <0 0 5 ;靶细胞出现细胞固缩、染色质凝聚和边集 ;产生梯状DNA并检测到亚二倍体峰(凋亡峰 ) ;同时 ,G0 /G1期细胞增多 ,S期细胞减少。结论 :金喜素可抑制人肝癌HCC772 1细胞增殖 ,使细胞阻滞在G0 /G1期 ,进一步诱导细胞凋亡。 OBJECTIVE:To study the proapoptotic effects of topotecan (TPT) on human liver cancer HCC7721 cells.METHODS:The cytotoxic effect of topotecan on HCC7721 cells was measured by MTT assay, the morphological changes observed by a eletronic microscope, DNA fragmentation detected by agarose gel electrophoresis, and the cell cycles and DNA content detected by flow cytometry.RESULTS:After incubated with 0.3 μmol/L topotecan for 6 h, 12 h, 24 h and 36 h, the survival rates in HCC7721 cells significantly reduced to (83±16)%,(69±10)%,(52±13)% and (30±11)%,P<0.05,respectively Targeted cells demonstrated cell shrinkage, chromatin condensation and margination. Ladder DNA and aneuploid peak were detected. Meanwhile, treated by topotecan for 24 h, there was a remarkable accumulation of cells in the G 0/G 1 phase of the cell cycles, and the cells in S phase declined.CONCLUSION:Topotecan can inhibit proliferation in human liver cancer HCC7721 cells,with G 0/G 1 arrest and induction of apoptosis.
出处 《肿瘤防治杂志》 2004年第11期1163-1165,共3页 China Journal of Cancer Prevention and Treatment
关键词 肝肿瘤/病理学 细胞死亡 细胞周期 liver neoplasms/pathology cell death cell cycle
  • 相关文献

参考文献8

  • 1吴桂芝,冯端浩,刘蔚,孙玲,张显杰.羟基喜树碱对家兔环孢A代谢和红细胞膜脂流动性的影响[J].中国药理学通报,2001,17(1):94-96. 被引量:2
  • 2Vey N,Kantarjian H,Beran M,et al. Combination of topotecan with cytarabine or etoposide in patients with refractory or relapsed acute myeloid leukemia: results of a randomised phase Ⅰ /Ⅱ study[J]. Ivest NewDrugs,1999,17(1):89-95.
  • 3Vaux D L,Stresser A. The molecular biology of apoptosis[J].Proc Natl Acad Sci U S A,1996,93(6):2239-2244.
  • 4Budihardjo I,Oliver H,Lutler M,et al. Biochemical pathways of caspase activation during apoptosis[J]. Annu Rev Cell Dev Biol,1999,15(1) :269-290.
  • 5Hengartner M O. The biochemistry of apoptosis[J]. Nature,2000,407(3) ;770-775.
  • 6Wolf B B, Green D R. Suicidal tendencies: Apoptotic cell death by caspase family proteinase[J]. J Biol Chem. 2000. 274 (11): 20049-20052.
  • 7陈协群,万幼峰,曹云新.金喜素诱导HL-60细胞凋亡依赖caspase活化[J].中国药理学通报,2001,17(6):650-653. 被引量:6
  • 8Kim J M, Luo L,Zirkin B R. Caspase 3 activation is repuired for leydig cell apoptosis induced by ethane dimethanesulfonate[J].Endocrinology, 2000,141(5): 1846- 1853.

二级参考文献9

共引文献6

同被引文献20

  • 1苗劲蔚,孔为民,牛巨伟,张卫华,邓小虹.吉西他滨对人子宫颈癌HeLa细胞系的放射增敏作用[J].北京医学,2004,26(4):244-246. 被引量:4
  • 2何芬,吴敬波.拓扑替康及其放射增敏效应研究进展[J].中国肿瘤,2004,13(11):727-730. 被引量:2
  • 3王薇,柯舜安,邬素芳,李静,陈刚,李辅军,王世宣,卢运萍,马丁.拓扑替康诱导人卵巢癌顺铂耐药细胞株COC1/DDP凋亡的研究[J].实用妇产科杂志,2005,21(5):276-278. 被引量:2
  • 4卢玉波,杨宏英,魏万里,杨谢兰,董菊颖.拓扑替康在宫颈癌治疗中的抗癌效应[J].肿瘤学杂志,2005,11(4):263-264. 被引量:1
  • 5Bose R,Verheij M,Haimojtz-Friedman A,et al.Ceramide synthase mediates daunorubin-induce apoptosis:an alternative mechanism for generating death signals[J].Cell,1995,82(3):405-414.
  • 6Huang X,Halicka H D,Traganos F,et al.Cytometric assessment of DNA damage in relation to cell cycle phase and apoptosis[J].Cell Prolif,2005,38(4):223-243.
  • 7Tamm I,Schriever F,Dorken B.Apoptosis:implications of basic research for clinical oncology[J].Lancet Oncol,2001,2(1):33-42.
  • 8Muggia F M.Recent updates in the clinical use of platinum compounds for the treatment of gynecologic cancers[J].Semin Oncol,2004,31(6 Suppl 14):17-24.
  • 9Lopez-saez J F,de la Torre C,Pincheire J,et al.Cell proliferaton and cancer[J].Histol Histopathol,1998,13 (4):1197-1214.
  • 10Walboomers J M,Jacobs M V,Manos M M,et al.Human papillomavirus is a necessary cause of invasive cervical cancer worldwide[J].J Pathol,1999,189 (1):12-19.

引证文献2

二级引证文献13

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