期刊文献+

PAC-1,L-OHP单用及联合用药对人结肠癌细胞的抑制作用 被引量:3

The inhibition of PAC-1,L-OHP and PAC-1 plus L-OHP on the human colorectal cancer cell
原文传递
导出
摘要 目的观察体外单用及两者联合应用半胱天冬酶原活化复合物-1(PAC-1)和奥沙利铂(L-OHP)对人结肠腺癌细胞株HCT116、SW480、HT-29,SW116和SW620的生长抑制作用。方法 MTT法检测两药单用和合用前后对细胞增殖活性的影响。结果 PAC-1和L-OHP单用对5种人结肠癌细胞均有明显的诱导凋亡和增殖抑制作用,并呈时间和浓度依赖性;PAC-1对上述细胞的半数抑制浓度(IC50)之间无统计学差异(P>0.05),L-OHP对上述细胞的的IC50值有统计学意义(P<0.05)。PAC-1与L-OHP联用(同时给药)产生拮抗作用(CI(1)。结论 PAC-1与L-OHP单用均对人结肠腺癌细胞有抑制作用,但各细胞株对两药的敏感性不同,两者联合应用(同时给药)起拮抗作用。 Objective To investigate the inhibition of procaspase-activating compound-1(PAC-1),Oxaliplatin(L-OHP) and PAC-1 conbination with L-OHP on human colorectal cancer cell lines (HT-29,SW116,HCT116,SW620,SW480).Methods MTT assay was used to investigate the proliferation of cells before and after single and combined drug use.Results Both PAC-1 and L-OHP had signficant high effect of inducing apoptosis and inhibiting proliferation on five human colorectal cancer cells on a dose and time dependent manner.The IC50 of PAC-1 on different human colorectal cancer cells had no statistical significance(P0.05); but IC50 of L-OHP on the 5 cell lines had statistical significance(P0.05).PAC-1 combined with L-OHP (dosing pump at the same time)had an antagonistic effect(CI﹥1).Conclusions Both PAC-1 and L-OHP can inhibit human colorectal cancer cell lines,but the susceptibility of individual colorectal cancer cell lines on the two drugs are different.PAC-1 combined with L-OHP has an antagonistic effect.
出处 《中国普通外科杂志》 CAS CSCD 北大核心 2010年第10期1097-1102,共6页 China Journal of General Surgery
关键词 半胱天冬酶原活化复合物-1 奥沙利铂 结肠癌 药物敏感性 procaspase-activating compound-1(PAC-1) oxaliplatin(L-OHP) colorectal cancer drug susceptibility
  • 相关文献

参考文献4

二级参考文献42

  • 1杨连君,司晓辉.EXPRESSION AND SIGNIFICANCE OF CYCLIN D1 IN HUMAN HEPATOCELLULAR CARCINOMA[J].Chinese Journal of Cancer Research,2001,13(2):144-146. 被引量:7
  • 2艾军,梁索源,单保恩,何兰欣,任金荣.食管癌患者外周血淋巴细胞替代肿瘤细胞体外药敏试验相关性研究[J].癌变.畸变.突变,2006,18(1):58-60. 被引量:7
  • 3Mosmann T. Rapid colometric assay for celular growth and survival: application to proliferation and cytotoxicity assay[J]. J Immunol Meth, 1983,65(1-2):55~63.
  • 4Hongo T,Fujii Y, Igarashi Y. An in vitro chemosensitivity test for the screening of anti-cancer drug in childhood leukemia[J]. Cancer, 1990,65(6): 1263~ 1272.
  • 5Yamada S, Hongo T, Okada S,et al. Clinical relevance of in vitro chemoresistance in childhood acute myeloid leukemia[J]. Leukemia, 2001,15(12):1892~1897.
  • 6Kubota T, Egawa T, Otani Y, etal. Cancer chemotherapy chemosensitivity testing is useful in evaluating the appropriate adjuvant cancer chemotherapy for stages Ⅲ/Ⅳ gastric cancers without peritoneal dissemination[J]. Anticancer Res, 2003, 23 (1B):583~587.
  • 7Kabeshima Y, Kubota T, Watanabe M, et al. Clinical usefulness of chemosensitivity test for advanced colorectal cancer[J]. Anticancer Res, 2002,22(5) :3033~3037.
  • 8Taylor CG,Sargent JM,Elgie AW,et al. Chemosensitivity testing predicts survival in ovarian cancer[J]. Eur J Gynaecol Oncol,2001,22 (4):278~282.
  • 9Sargent JM. The use of the MTT assay to study drug resistance in fresh tumour samples[J]. Recent Results Cancer Res,2003,161:13~25.
  • 10Levi F. From circadian to cancer chronotherapeutics [ J]. Chronobiol Internat, 2002, 19( 1 ) :1-19.

共引文献36

同被引文献4

引证文献3

二级引证文献11

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