期刊文献+

酒石酸锑钾诱导人结肠癌细胞凋亡 被引量:1

Potassium Antimonyl Tartrate Induces Apoptosis of Human Colon Cancer Cells
原文传递
导出
摘要 目的 研究表明酒石酸锑钾能抑制白血病细胞及淋巴瘤细胞生长,并诱导其凋亡。本研究旨在探讨酒石酸锑钾诱导人结肠癌SW480凋亡的作用。方法 将不同浓度酒石酸锑钾作用于体外培养人结肠癌SW480细胞。采用MTT法检测酒石酸锑钾对结肠癌SW480细胞的生长抑制作用,并计算生长抑制率;流式细胞术检测亚二倍体峰,并利用TUNEL法进行凋亡的分子生物学检测。结果 酒石酸锑钾能明显抑制结肠癌细胞生长,抑制作用呈时间和剂量依赖性;流式细胞仪检测到亚二倍体峰,亚二倍体细胞比例随时间延长而增加。TUNEL法观察到棕褐色着染的凋亡阳性细胞。结论 酒石酸锑钾能抑制SW480细胞生长并诱导细胞凋亡。 Objective This study was designed to investigate whether potassium antimonyl tartrate can induce apoptosis in human colon cancer cells (SGC-7901) in vitro,which provide experiment evidence for colon cancer therapy.Methods The growth inhibition of cells induced by various concentrations of PAT in different time course was analyzed by using MTT assay.The flow cytomery and terminal deoxynucleotidyl transferase-mediated duttp-biotin nick nedlabel (TNNEL) were applied to detect apoptotic cells.Results Potassium antimonyl tartrate inhibited SW480 cells growth significantly in does dependent and time dependent manner.DNA histograms showed the hypodiploid peak,the ration of hypodiploid cells was increased with the increase of dose and elongation of time.Bown-color positive apoptotic cells were observed with TUNEL method.Conclusion Potassium antimonyl tartrat can inhibit the proliferation of SW480 cells and induce apoptosis.
出处 《临床消化病杂志》 2005年第1期12-13,共2页 Chinese Journal of Clinical Gastroenterology
基金 湖北省教育厅基金资助项目(2000A43003)
关键词 酒石酸锑钾 结肠癌 凋亡 Potassium antimonyl tartrate Colon cancer Apoptosis
  • 相关文献

参考文献4

二级参考文献18

  • 1[1]Tian X, Wsng YG, Yang MG, etal. Synthesis and antitumor activity ot spin labeled derivatives of podophyllotoxin. Life Sci, 1997,60:511.
  • 2[3]Kerr JF, Winterford CM, Harmon BY. Apoptosis: its singnificance in cancer and cancer therapy. Lancet, 1997,73: 2013.
  • 3[5]Hino N, Higashi T, Nouso K. Apoptosis and proliferation of human heptocellular carcinoma. Liver, 1996,16:123.
  • 4[6]Milluer M. Drug-induced apoptosis in hepatoma cells is mediated by the CD95(APO-1/fas recptor)ligand system and involves actlvation of wild-type p53. Clin Invest, 1997,99:403.
  • 5[7]Bamard JA, Lyons RM, Moses HL. The cell biology of transforming growth factor-β. Biochem Biophys Acta, 1990, 1032:79.
  • 6[8]Fukuda K,Kojiro M, Chiu JF.Induction of apoptosis by transforming growth factor-β1 in the rat hepatoma cell line Mc A-RH7777: a possible assosiation with tissue transglutaminase expression . Hepatology, 1993,18: 954.
  • 7[9]Abou-Shady M, Baer HU, Friess H, et al. Transforming growth factor beta and their signaling receptors in human hepatocellular carcinoma. Am J Srug,1999,177(3) :209
  • 8Kagawa S,Pearson SA,Ji L,et al.A binary adenoviral vector system for expressing high levels of the proapoptotic gene bax[].Gene Therapy.2000
  • 9Arai H,Gordon D,Nabel EG,et al.Gene transfer of Fas ligand induces tumor regression in vivo[].Proceedings of the National Academy of Sciences of the United States of America.1997
  • 10Ashkenazi A,Pai RC,Fong S,et al.Safety and antitumor activity of recombinant soluble Apo2 ligand[].The Journal of Clinical Investigation.1999

共引文献8

同被引文献12

引证文献1

二级引证文献2

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