Proteasome inhibition with PS-341 (bortezomib) in lung cancer therapy

被引:27
|
作者
Lara, PN
Davies, AM
Mack, PC
Mortenson, MM
Bold, RJ
Gumerlock, PH
Gandara, DR
机构
[1] Univ Calif Davis, Dept Internal Med, Div Hematol Oncol, Sacramento, CA 95817 USA
[2] Univ Calif Davis, Dept Surg, Sacramento, CA 95817 USA
[3] UCD, Canc Ctr, Sch Med, Sacramento, CA USA
关键词
D O I
10.1053/j.seminoncol.2003.12.013
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PS-341 (bortezomib) represents a new class of therapeutics that targets the ubiquitin-proteasome pathway. It has broad-spectrum single-agent anticancer activity and can potentiate chemotherapy and radiation in preclinical models. Early phase clinical studies have shown tolerability and activity in multiple myeloma, lymphoma, prostate cancer, and lung cancers. By its mechanism of inhibiting protein degradation, PS-341 targets a wide range of pathways relevant to tumor progression and therapy resistance and can directly modulate expression of cyclins, p27Kip1, p53, nuclear factor-κB, Bcl-2, and Bax. PS-341 is currently in phase I/II clinical development in both non-small cell lung cancer and small cell lung cancer. This article will review the preclinical and clinical experience with PS-341 as it relates to lung cancer. © 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:40 / 46
页数:7
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