The immunophannacology of paclitaxel (Taxol®) docetaxel (Taxotere®), and related agents

被引:91
作者
Fitzpatrick, FA
Wheeler, R
机构
[1] Univ Utah, Dept Oncol Sci, Huntsman Canc Inst, Salt Lake City, UT 84103 USA
[2] Univ Utah, Dept Med Chem, Huntsman Canc Inst, Salt Lake City, UT 84103 USA
[3] Univ Utah, Dept Internal Med, Huntsman Canc Inst, Salt Lake City, UT 84103 USA
关键词
paclitaxel; docetaxel; structure-activity relationships;
D O I
10.1016/j.intimp.2003.08.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Paclitaxel (Taxol((R))) and docetaxel (Taxotere((R))) are among the most unique, and successful, chemotherapeutic agents used for the treatment of breast and ovarian cancer. Both agents have anti-mitotic properties derived from binding to tubulin and excessive stabilization of microtubules. Their anti-neoplastic effects derive from this mechanism. Distinct from their effects on microtubule stabilization, paclitaxel, docetaxel, and related taxanes display immunopharmacological traits. In this review, we discuss their induction of pro-inflammatory genes and proteins; the current hypotheses on the molecular mechanism for this induction, especially its relationship to the lipopolysaccharide (LPS) signaling pathway. We also discuss the structure-activity relationships (SAR) that govern gene induction, especially the striking differences between the SAR for murine and human cells in vitro. Lastly, we discuss the immunopharmacological traits of paclitaxel and docetaxel in terms of their relevance to human clinical pharmacology and toxicology and their activity in animal models of autoimmune disorders. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:1699 / 1714
页数:16
相关论文
共 101 条
[1]  
Arsenault AL, 2000, J RHEUMATOL, V27, P582
[2]   Drug interactions with the taxanes: clinical implications [J].
Baker, AF ;
Dorr, RT .
CANCER TREATMENT REVIEWS, 2001, 27 (04) :221-233
[3]  
Bernstein BJ, 2000, ANN PHARMACOTHER, V34, P1332
[4]  
Bhat N, 1999, J IMMUNOL, V162, P7335
[5]  
Blagosklonny MV, 1999, INT J CANCER, V83, P151, DOI 10.1002/(SICI)1097-0215(19991008)83:2<151::AID-IJC1>3.0.CO
[6]  
2-5
[7]   TAXOL, A MICROTUBULE-STABILIZING ANTINEOPLASTIC AGENT, INDUCES EXPRESSION OF TUMOR-NECROSIS-FACTOR-ALPHA AND INTERLEUKIN-1 IN MACROPHAGES [J].
BOGDAN, C ;
DING, A .
JOURNAL OF LEUKOCYTE BIOLOGY, 1992, 52 (01) :119-121
[8]   REGRESSION OF COLLAGEN-INDUCED ARTHRITIS WITH TAXOL, A MICROTUBULE STABILIZER [J].
BRAHN, E ;
TANG, C ;
BANQUERIGO, ML .
ARTHRITIS AND RHEUMATISM, 1994, 37 (06) :839-845
[9]  
BURKHART CA, 1994, CANCER RES, V54, P5779
[10]   Heat shock protein 90 mediates macrophage activation by Taxol and bacterial lipopolysaccharide [J].
Byrd, CA ;
Bornmann, W ;
Erdjument-Bromage, H ;
Tempst, P ;
Pavletich, N ;
Rosen, N ;
Nathan, CF ;
Ding, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (10) :5645-5650