The inhibitor of apoptosis protein family (IAPs): an emerging therapeutic target in cancer

被引:227
作者
Nachmias, B [1 ]
Ashhab, Y [1 ]
Ben-Yehuda, D [1 ]
机构
[1] Hadassah Univ Hosp, Dept Hematol, IL-91120 Jerusalem, Israel
关键词
apoptosis; cancer; IAP; caspase; molecular targets;
D O I
10.1016/j.semcancer.2004.04.002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Apoptosis is a crucial biological process that prevents uncontrolled cell proliferation and eliminates harmful cells. Resistance to apoptotic stimuli is a hallmark feature of various cancers. One of the mechanisms through which tumor cells are believed to acquire resistance to apoptosis is by overexpression of inhibitor of apoptosis proteins (IAPs). IAPs are a group of structurally related proteins that were initially identified in baculoviruses. Mammalian IAPs block apoptosis either by binding and inhibiting caspases or through caspase-independent mechanisms. This family of proteins has become increasingly prominent in the field of cancer biology. To date, overexpression of several IAPs has been detected in various cancers. This paper reviews the recent advances in the research of IAPs. The differential expression and the biological significance of each IAP in various cancer types will be discussed. Finally, we review the most recent advances in the research efforts aimed at using IAPs as potential targets for cancer therapy. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:231 / 243
页数:13
相关论文
共 145 条
[1]   Expression and prognostic significance of survivin in de novo acute myeloid leukaemia [J].
Adida, C ;
Recher, C ;
Raffoux, E ;
Daniel, MT ;
Taksin, AL ;
Rousselot, P ;
Sigaux, F ;
Degos, L ;
Altieri, DC ;
Dombret, H .
BRITISH JOURNAL OF HAEMATOLOGY, 2000, 111 (01) :196-203
[2]  
Adida C, 2000, BLOOD, V96, P1921
[3]  
Allen SM, 2003, CANCER RES, V63, P567
[4]   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
[5]   Cyclic adenosine-3',5'-monophosphate production is greater in rabbit duodenal crypt than in villus cells [J].
Amelsberg, M ;
Amelsberg, A ;
Ainsworth, MA ;
Hogan, DL ;
Isenberg, JI .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1996, 31 (03) :233-239
[6]   The melanoma inhibitor of apoptosis protein: A target for spontaneous cytotoxic T cell responses [J].
Andersen, MH ;
Reker, S ;
Becker, JC ;
Straten, PT .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2004, 122 (02) :392-399
[7]   Inhibition of survivin expression suppresses the growth of aggressive non-Hodgkin's lymphoma [J].
Ansell, SM ;
Arendt, BK ;
Grote, DM ;
Jelinek, DF ;
Novak, AJ ;
Wellik, LE ;
Remstein, ED ;
Bennett, CF ;
Fielding, A .
LEUKEMIA, 2004, 18 (03) :616-623
[8]   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
[9]   Two splicing variants of a new inhibitor of apoptosis gene with different biological properties and tissue distribution pattern [J].
Ashhab, Y ;
Alian, A ;
Polliack, A ;
Panet, A ;
Ben Yehuda, D .
FEBS LETTERS, 2001, 495 (1-2) :56-60
[10]  
Badran A, 2003, ANTICANCER RES, V23, P589