Novel therapeutic targets in lung cancer: Inhibitor of apoptosis proteins from laboratory to clinic

被引:40
作者
Dean, Emma J.
Ranson, Malcolm
Blackhall, Fiona
Holt, Sarah V.
Dive, Caroline
机构
[1] Christie Hosp NHS Trust, Manchester M20 4BX, Lancs, England
[2] Univ Manchester, Paterson Inst Canc Res, Manchester M20 4BX, Lancs, England
关键词
inhibitors of apoptosis; X-tinked inhibitor of apoptosis protein; apoptosis; antisense; small molecules; non-small cell; lung cancer; small cell lung cancer;
D O I
10.1016/j.ctrv.2006.11.002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Lung cancer is the leading cause of cancer death worldwide. Despite the introduction of new agents and schedules, chemotherapy still obtains unsatisfactory overall response rates, rare complete remissions and responses of relatively short duration. The inhibitor of apoptosis proteins (IAPS) are a family of caspase inhibitors that selectively bind and inhibit caspases-3, -7, and -9. As caspase activation is central to apoptosis, novel therapeutic drugs that target IAPs enabling apoptosis to occur have potential as a treatment of malignancy. Several agents that target core components of the apoptotic signalling pathway are currently at an early stage of development. This review reports the progress being made in characterising the IAP family, with a focus on the available data relevant to the treatment of lung cancer. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:203 / 212
页数:10
相关论文
共 106 条
[1]   A novel anti-apoptosis gene, survivin, expressed in cancer and lymphoma [J].
Ambrosini, G ;
Adida, C ;
Altieri, DC .
NATURE MEDICINE, 1997, 3 (08) :917-921
[2]   Synthetic Smac/DIABLO peptides enhance the effects of chemotherapeutic agents by binding XIAP and cIAP1 in situ [J].
Arnt, CR ;
Chiorean, MV ;
Heldebrant, MV ;
Gores, GJ ;
Kaufmann, SH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (46) :44236-44243
[3]   Endogenously released Smac is insufficient to mediate cell death of human lung carcinoma in response to etoposide [J].
Bartling, B ;
Lewensohn, R ;
Zhivotovsky, B .
EXPERIMENTAL CELL RESEARCH, 2004, 298 (01) :83-95
[4]   Increased expression of apoptosis inhibitor protein XIAP contributes to anoikis resistance of circulating human prostate cancer metastasis precursor cells [J].
Berezovskaya, O ;
Schimmer, AD ;
Glinskii, AB ;
Pinilla, C ;
Hoffman, RM ;
Reed, JC ;
Glinsky, GV .
CANCER RESEARCH, 2005, 65 (06) :2378-2386
[5]   AN APOPTOSIS-INHIBITING GENE FROM A NUCLEAR POLYHEDROSIS-VIRUS ENCODING A POLYPEPTIDE WITH CYS/HIS SEQUENCE MOTIF [J].
BIRNBAUM, MJ ;
CLEM, RJ ;
MILLER, LK .
JOURNAL OF VIROLOGY, 1994, 68 (04) :2521-2528
[6]   XIAP and survivin as therapeutic targets for radiation sensitization in preclinical models of lung cancer [J].
Cao, C ;
Mu, Y ;
Hallahan, DE ;
Lu, B .
ONCOGENE, 2004, 23 (42) :7047-7052
[7]   Apaf-1/cytochrome c-independent and Smac-dependent induction of apoptosis in multiple myeloma (MM) cells [J].
Chauhan, D ;
Hideshima, T ;
Rosen, S ;
Reed, JC ;
Kharbanda, S ;
Anderson, KC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (27) :24453-24456
[8]   Downregulation of Bcl-2, FLIP or IAPs (XIAP and survivin) by siRNAs sensitizes resistant melanoma cells to Apo2L/TRAIL-induced apoptosis [J].
Chawla-Sarkar, M ;
Bae, SI ;
Reu, FJ ;
Jacobs, BS ;
Lindner, DJ ;
Borden, EC .
CELL DEATH AND DIFFERENTIATION, 2004, 11 (08) :915-923
[9]  
CHECINSKA H, 2006, AACR M, P563
[10]   A human IAP-family gene, Apollon, expressed in human brain cancer cells [J].
Chen, ZH ;
Naito, M ;
Hori, S ;
Mashima, T ;
Yamori, T ;
Tsuruo, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 264 (03) :847-854