Paclitaxel-induced FasL-independent apoptosis and slow (non-apoptotic) cell death

被引:42
作者
Blagosklonny, MV
Robey, R
Sheikh, MS
Fojo, T
机构
[1] NCI, Med Branch, NIH, Bethesda, MD 20892 USA
[2] New York Med Coll, Dept Med, Valhalla, NY 10595 USA
[3] SUNY Upstate Med Univ, Dept Pharmacol, Syracuse, NY 13210 USA
关键词
microtubule-active drugs; caspases; mitotic slippage; multinucleation;
D O I
10.4161/cbt.53
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Microtubule-active drugs, including paclitaxel (Taxol, PTX), cause mitotic arrest, and this can result in apoptosis. A recently study has reported that PTX mediates apoptosis by upregulating FasL in Jurkat and MDA-231 cells. In contrast to the previous report, we found that anti-FasL antibodies failed to inhibit PTX-induced apoptosis in Jurkat cells. In MDA-231 cells, neither FasL nor PTX induced apoptosis. In these cells, PTX caused slow cell death without activation of caspase-3 or -8 or PARP cleavage. Doxorubicin at cytostatic concentrations did not affect FasL-induced apoptosis but inhibited PTX-induced apoptosis in Jurkat cells. Following PTX-induced mitotic arrest Jurkat cells undergo apoptosis, whereas MDA-MB-231 cells exit mitosis and form multinucleated cells which then die in a slower nonapoptotic manner.
引用
收藏
页码:113 / 117
页数:5
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