Selective anticancer strategies via intervention of the death pathways relevant to cell transformation

被引:35
作者
Li, Q-X [1 ]
Yu, D. H. [1 ]
Liu, G. [1 ]
Ke, N. [1 ]
McKelvy, J. [1 ]
Wong-Staal, F. [1 ]
机构
[1] iTherX Pharmaceut Inc, Drug Dev, San Diego, CA 92121 USA
关键词
cancer; target; drug; cell adhesion; UPR; GRP78; virotherapy;
D O I
10.1038/cdd.2008.48
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Apoptosis is an important physiological process that promotes tissue homeostasis by eliminating unnecessary or malfunctioning cells. Abnormality in this process contributes to tumorigenesis, as well as the resistance to cancer treatment by radiation and chemotherapy. Restoration of normal apoptosis would not only promote cancer cell death and halt tumor progression, but also increase the response to many current cancer therapies. Although apoptosis induction is an important principle of currently used radiation and chemotherapy treatment, uncovering the mechanisms that govern this process, and which are lost during transformation, represents an important direction for realizing improved therapies for the future. This article first briefly reviews aspects of current discovery strategies for new anticancer therapeutics based on intervening in cell death pathways, and then discusses in more detail several cancer-relevant death pathways, which are disabled during transformation and which can be targeted therapeutically. These include anoikis/cell adhesion; energy metabolism and the unfolded protein response. Finally, we introduce a new concept, which utilizes cancer-specific apoptosis induced by oncolytic viruses. The discussion of these topics involves novel targets, compounds and virotherapy.
引用
收藏
页码:1197 / 1210
页数:14
相关论文
共 108 条
[1]   Evaluation of 2-deoxy-D-glucose as a chemotherapeutic agent: mechanism of cell death [J].
Aft, RL ;
Zhang, FW ;
Gius, D .
BRITISH JOURNAL OF CANCER, 2002, 87 (07) :805-812
[2]   Inhibition of glutamate cysteine ligase activity sensitizes human breast cancer cells to the toxicity of 2-deoxy-D-glucose [J].
Andringa, KK ;
Coleman, NC ;
Aykin-Burns, N ;
Hitchler, NJ ;
Walsh, SA ;
Domann, FE ;
Spitz, DR .
CANCER RESEARCH, 2006, 66 (03) :1605-1610
[3]   Cell surface expression of the stress response chaperone GRP78 enables tumor targeting by circulating ligands [J].
Arap, MA ;
Lahdenranta, J ;
Mintz, PJ ;
Hajitou, A ;
Sarkis, AS ;
Arap, W ;
Pasqualini, R .
CANCER CELL, 2004, 6 (03) :275-284
[4]   p53 inhibits α6β4 integrin survival signaling by promoting the caspase 3-dependent cleavage of AKT/PKB [J].
Bachelder, RE ;
Ribick, MJ ;
Marchetti, A ;
Falcioni, R ;
Soddu, S ;
Davis, KR ;
Mercurio, AM .
JOURNAL OF CELL BIOLOGY, 1999, 147 (05) :1063-1072
[5]   Chronic myeloid leukaemia: an investigation into the role of Bcr-Abl-induced abnormalities in glucose transport regulation [J].
Barnes, K ;
McIntosh, E ;
Whetton, AD ;
Daley, GQ ;
Bentley, J ;
Baldwin, SA .
ONCOGENE, 2005, 24 (20) :3257-3267
[6]   Adhesion dependent signalling in the tumour microenvironment: The future of drug targetting [J].
Bewick, Mary A. ;
Lafrenie, Robert M. .
CURRENT PHARMACEUTICAL DESIGN, 2006, 12 (22) :2833-2848
[7]  
Boylan MO, 1996, CELL GROWTH DIFFER, V7, P725
[8]   Targeted induction of apoptosis for cancer therapy: current progress and prospects [J].
Bremer, Edwin ;
van Dam, Go ;
Kroesen, Bart Jan ;
de Leij, Lou ;
Helfrich, Wijnand .
TRENDS IN MOLECULAR MEDICINE, 2006, 12 (08) :382-393
[9]   Restoration of the tumor suppressor function to mutant p53 by a low-molecular-weight compound [J].
Bykov, VJN ;
Issaeva, N ;
Shilov, A ;
Hultcrantz, M ;
Pugacheva, E ;
Chumakov, P ;
Bergman, J ;
Wiman, KG ;
Selivanova, G .
NATURE MEDICINE, 2002, 8 (03) :282-288
[10]  
Cai SX, 2006, CURR MED CHEM, V13, P2627