Synergistic effect of paclitaxel and 4-hydroxytamoxifen on estrogen receptor-negative colon cancer and lung cancer cell lines

被引:16
作者
Gu, WZ [1 ]
Chen, ZH [1 ]
Tahir, SK [1 ]
Rosenberg, SH [1 ]
Ng, SC [1 ]
机构
[1] Abbott Labs, Pharmaceut Prod Res Div, Dept 4N6, Abbott Pk, IL 60065 USA
关键词
apoptosis; cancer; combination treatment; cell cycle; paclitaxel; tamoxifen;
D O I
10.1097/00001813-199911000-00005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Antiestrogen tamoxifen (Tam) is the most prescribed drug for the treatment of estrogen receptor (ER)-positive breast cancers. It is also used in long-term clinical trials with encouraging preliminary results as a chemopreventive agent far breast cancer. The effect of Tam an ER-negative cancers, however, is unclear. Here we reported that paclitaxel and 4-hydroxytamoxifen (4-HT) have a synergistic cytotoxic effect on the ER-negative colon cancer cell line HCT15, which is refractory to paclitaxel atone. Our results showed that 4-HT at submicromolar concentrations effectively enhanced the antiproliferative effect of paclitaxel. In addition, at 1/10 of the paclitaxel concentrations used for HCT15, 4-HT and paclitaxel also showed synergistic effect on NCI H460, an ER-negative lung cancer cell line. For both cell lines, the effective concentration for paclitaxel to inhibit cell growth was 1 log lower in the combination treatment than the concentration used in the single treatment. Cell cycle analysis showed that the combination of paclitaxel and 4-HT increased the G(2)/M population and resulted in the increase of apoptosis in both cell lines. Enhanced early release of cytochrome c from mitochondria may be the apoptotic pathway activated in the combination treatment in HCT15 cells. [(C) 1999 Lippincott Williams & Wilkins.].
引用
收藏
页码:895 / 901
页数:7
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