How Taxol/paclitaxel kills cancer cells

被引:1118
作者
Weaver, Beth A. [1 ,2 ]
机构
[1] Univ Wisconsin, Dept Cell & Regenerat Biol, Madison, WI 53705 USA
[2] Univ Wisconsin, Carbone Canc Ctr, Madison, WI 53705 USA
基金
美国国家卫生研究院;
关键词
1ST TOTAL-SYNTHESIS; MITOTIC CHECKPOINT; PROTEIN-TAU; IN-VIVO; TAXOL; MICROTUBULES; PACLITAXEL; APOPTOSIS; SENSITIVITY; RESPONSES;
D O I
10.1091/mbc.E14-04-0916
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Taxol (generic name paclitaxel) is a microtubule-stabilizing drug that is approved by the Food and Drug Administration for the treatment of ovarian, breast, and lung cancer, as well as Kaposi's sarcoma. It is used off-label to treat gastroesophageal, endometrial, cervical, prostate, and head and neck cancers, in addition to sarcoma, lymphoma, and leukemia. Paclitaxel has long been recognized to induce mitotic arrest, which leads to cell death in a subset of the arrested population. However, recent evidence demonstrates that intratumoral concentrations of paclitaxel are too low to cause mitotic arrest and result in multipolar divisions instead. It is hoped that this insight can now be used to develop a biomarker to identify the similar to 50% of patients that will benefit from paclitaxel therapy. Here I discuss the history of paclitaxel and our recently evolved understanding of its mechanism of action.
引用
收藏
页码:2677 / 2681
页数:5
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