Potential and caveats of TRAIL in cancer therapy

被引:64
作者
Held, J [1 ]
Schulze-Osthoff, K [1 ]
机构
[1] Univ Munster, Dept Immunol & Cell Biol, D-48149 Munster, Germany
关键词
D O I
10.1054/drup.2001.0208
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Induction of apoptosis in tumor cells is a major goal for chemotherapy and radiation treatment strategies. However, disordered gene expression often leads to apoptosis resistance rendering tumor cells insensitive to various conventional treatments. TNF-related apoptosis-inclucing ligand (TRAIL) is a recently identified cytokine of the TNF superfamily that induces apoptosis in tumor cells upon binding to different receptors. Remarkably, the majority of tumor cell lines are sensitive to TRAIL-induced apoptosis, while most nontransformed cell types are TRAIL-resistant. Furthermore, a combination treatment of TRAIL with ionizing irradiation or chemotherapeutic agents induces apoptosis in a highly synergistic manner, particularly in those cells that are otherwise resistant to a sole treatment. In contrast to other TNF members, TRAIL apparently does not exert overt systemic toxicity in murine and primate models, although unexpected concerns about a potential hepatotoxicity of TRAIL have been recently raised. While the molecular mechanisms of TRAIL sensitivity and resistance are poorly understood, TRAIL seems to be a promising biological agent for combination therapy with chemotherapeutic drugs or irradiation. (C) 2001 Harcourt Publishers Ltd.
引用
收藏
页码:243 / 252
页数:10
相关论文
共 121 条
[41]   TRAIL (Apo2 ligand) and TWEAK (Apo3 ligand) mediate CD4+ T cell killing of antigen-presenting macrophages [J].
Kaplan, MJ ;
Ray, D ;
Mo, RR ;
Yung, RL ;
Richardson, BC .
JOURNAL OF IMMUNOLOGY, 2000, 164 (06) :2897-2904
[42]   Type I interferons (IFNs) regulate tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) expression on human T cells: A novel mechanism for the antitumor effects of type IIFNs [J].
Kayagaki, N ;
Yamaguchi, N ;
Nakayama, M ;
Eto, H ;
Okumura, K ;
Yagita, H .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 189 (09) :1451-1460
[43]  
Kayagaki N, 1999, J IMMUNOL, V163, P1906
[44]  
Keane MM, 1999, CANCER RES, V59, P734
[45]   CYTOTOXICITY-DEPENDENT APO-1 (FAS/CD95)-ASSOCIATED PROTEINS FORM A DEATH-INDUCING SIGNALING COMPLEX (DISC) WITH THE RECEPTOR [J].
KISCHKEL, FC ;
HELLBARDT, S ;
BEHRMANN, I ;
GERMER, M ;
PAWLITA, M ;
KRAMMER, PH ;
PETER, ME .
EMBO JOURNAL, 1995, 14 (22) :5579-5588
[46]   Apo2L/TRAIL-dependent recruitment of endogenous FADD and caspase-8 to death receptors 4 and 5 [J].
Kischkel, FC ;
Lawrence, DA ;
Chuntharapai, A ;
Schow, P ;
Kim, KJ ;
Ashkenazi, A .
IMMUNITY, 2000, 12 (06) :611-620
[47]   NF-κB inducers upregulate cFLIP, a cycloheximide-sensitive inhibitor of death receptor signaling [J].
Kreuz, S ;
Siegmund, D ;
Scheurich, P ;
Wajant, H .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (12) :3964-3973
[48]   FADD is required for DR4-and DR5-mediated apoptosis - Lack of trail-induced apoptosis in FADD-deficient mouse embryonic fibroblasts [J].
Kuang, AA ;
Diehl, GE ;
Zhang, JK ;
Winoto, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (33) :25065-25068
[49]  
Lacour S, 2001, CANCER RES, V61, P1645
[50]   Differential hepatocyte toxicity of recombinant Apo2L/TRAIL versions [J].
Lawrence, D ;
Shahrokh, Z ;
Marsters, S ;
Achilles, K ;
Shih, D ;
Mounho, B ;
Hillan, K ;
Totpal, K ;
DeForge, L ;
Schow, P ;
Hooley, J ;
Sherwood, S ;
Pai, R ;
Leung, S ;
Khan, LL ;
Gliniak, B ;
Bussiere, J ;
Smith, CA ;
Strom, SS ;
Kelley, S ;
Fox, JA ;
Thomas, D ;
Ashkenazi, A .
NATURE MEDICINE, 2001, 7 (04) :383-385