Drug insight: cancer therapy strategies based on restoration of endogenous cell death mechanisms

被引:154
作者
Reed, John C. [1 ]
机构
[1] Burnham Inst Med Res, La Jolla, CA 92037 USA
来源
NATURE CLINICAL PRACTICE ONCOLOGY | 2006年 / 3卷 / 07期
关键词
apoptosis; Bcl-2; caspase; inhibitor of apoptosis (IAP); TRAIL;
D O I
10.1038/ncponc0538
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Cell death is a normal facet of human physiology, ensuring tissue homeostasis by offsetting cell production with cell demise. Neoplasms arise in part because of defects in physiological cell death mechanisms, contributing to pathological cell expansion. Defects in normal cell death pathways also contribute to cancer progression by permitting progressively aberrant cell behaviors, while also desensitizing tumor cells to immune-mediated attack, radiation, and chemotherapy. Through basic research, much has been learned about the molecular mechanisms responsible for cell turnover and how tumors escape cell death. By exploiting this knowledge base, several innovative strategies for eradicating malignancies have materialized that are based on restoration of natural pathways for cell autodestruction. Some of these strategies have advanced into human clinical trials. Several of the current strategies based on targeting core components of the cell death machinery for cancer therapy are reviewed here, and a summary of progress toward clinical applications is provided.
引用
收藏
页码:388 / 398
页数:11
相关论文
共 81 条
[1]
Altieri Dario C, 2003, Methods Mol Biol, V223, P533
[2]
Retinoic acid-induced apoptosis in leukemia cells is mediated by paracrine action of tumor-selective death ligand TRAIL [J].
Altucci, L ;
Rossin, A ;
Raffelsberger, W ;
Reitmair, A ;
Chomienne, C ;
Gronemeyer, H .
NATURE MEDICINE, 2001, 7 (06) :680-686
[3]
An adenovirus encoding proapoptotic Bax synergistically radiosensitizes malignant glioma [J].
Arafat, WO ;
Buchsbaum, DJ ;
Gómez-Navarro, J ;
Tawil, SA ;
Olsen, C ;
Xiang, JL ;
El-Akad, H ;
Salama, AM ;
Badib, AO ;
Stackhouse, MA ;
Curiel, DT .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2003, 55 (04) :1037-1050
[4]
Depsipeptide (FR901228) induces histone acetylation and inhibition of histone deacetylase in chronic lymphocytic leukemia cells concurrent with activation of caspase 8-mediated apoptosis and down-regulation of c-FLIP protein [J].
Aron, JL ;
Parthun, MR ;
Marcucci, G ;
Kitada, S ;
Mone, AP ;
Davis, ME ;
Shen, TS ;
Murphy, T ;
Wickham, J ;
Kanakry, C ;
Lucas, DM ;
Reed, JC ;
Grever, MR ;
Byrd, JC .
BLOOD, 2003, 102 (02) :652-658
[5]
Targeting death and decoy receptors of the tumour-necrosis factor superfamily [J].
Ashkenazi, A .
NATURE REVIEWS CANCER, 2002, 2 (06) :420-430
[6]
Rational design and real time, in-cell detection of the proapoptotic activity of a novel compound targeting Bcl-XL [J].
Becattini, B ;
Kitada, S ;
Leone, M ;
Monosov, E ;
Chandler, S ;
Zhai, DY ;
Kipps, TJ ;
Reed, JC ;
Pellecchia, M .
CHEMISTRY & BIOLOGY, 2004, 11 (03) :389-395
[7]
Mechanisms of caspase activation [J].
Boatright, KM ;
Salvesen, GS .
CURRENT OPINION IN CELL BIOLOGY, 2003, 15 (06) :725-731
[8]
Cartee L, 2003, MOL CANCER THER, V2, P83
[9]
Small-molecule XIAP inhibitors derepress downstream effector caspases and induce apoptosis of acute myeloid leukemia cells [J].
Carter, BZ ;
Gronda, M ;
Wang, ZL ;
Welsh, K ;
Pinilla, C ;
Andreeff, M ;
Schober, WD ;
Nefzi, A ;
Pond, GR ;
Mawji, IA ;
Houghten, RA ;
Ostresh, J ;
Brandwein, J ;
Minden, MD ;
Schuh, AC ;
Wells, RA ;
Messner, H ;
Chun, K ;
Reed, JC ;
Schimmer, AD .
BLOOD, 2005, 105 (10) :4043-4050
[10]
Identification of chelerythrine as an inhibitor of BclXL function [J].
Chan, SL ;
Lee, MC ;
Tan, KO ;
Yang, LK ;
Lee, ASY ;
Flotow, H ;
Fu, NY ;
Butler, MS ;
Soejarto, DD ;
Buss, AD ;
Yu, VC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (23) :20453-20456