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
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