Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) receptor-1 and receptor-2 agonists for cancer therapy

被引:45
|
作者
Fox, Norma Lynn [1 ]
Humphreys, Robin [1 ]
Luster, Troy A. [1 ]
Klein, Jerry [1 ]
Gallant, Gilles [1 ]
机构
[1] Human Genome Sci, Rockville, MD 20850 USA
关键词
Apomab; apoptosis; conatumumab; dulanermin; lexatumumab; mapatumumab; tigatuzumab; TRAIL; TRAIL-R1; TRAIL-R2; RENAL-CELL CARCINOMA; ANTI-DR5; MONOCLONAL-ANTIBODY; HODGKINS-LYMPHOMA-CELLS; IN-VITRO; PHASE-I; DEATH RECEPTORS; END-POINTS; ANTITUMOR-ACTIVITY; DEATH-RECEPTOR-5; ANTIBODY; TARGETING TRAIL-R1;
D O I
10.1517/14712590903319656
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Importance of the field: Agents that activate the TNF-related apoptosis-inducing ligand death receptors, TRAIL-R1 and TRAIL-R2, have attracted substantial attention and investment as potential anti-cancer therapies. Preclinical studies of TRAIL-R agonists indicate that they may be efficacious in a wide range of tumor types, especially when combined with chemotherapeutic agents. Areas covered in this review. The rationale for clinical development of TRAIL-R agonists is described, including the basis for combining these agents with other agents that modulate the 'checks and balances' of the apoptotic pathways. Accruing data that highlight differences between TRAIL-R1 and TRAIL-R2 that could affect the clinical significance of their specific agonists are described. The clinical experience to date with each of the agonists is summarized. What the reader will gain: The reader will gain an understanding of the rationale for the clinical development of TRAIL-R agonists, as well as the current status of clinical trials of these interesting new agents. Take home message: Ongoing clinical trials will provide important information regarding the future development of TRAIL-R agonists.
引用
收藏
页码:1 / 18
页数:18
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