On the TRAIL to successful cancer therapy? Predicting and counteracting resistance against TRAIL-based therapeutics

被引:238
作者
Dimberg, L. Y. [1 ]
Anderson, C. K. [1 ]
Camidge, R. [2 ]
Behbakht, K. [1 ]
Thorburn, A. [3 ]
Ford, H. L. [1 ,3 ]
机构
[1] Univ Colorado, Sch Med, Dept Obstet & Gynecol, Aurora, CO 80045 USA
[2] Univ Colorado, Sch Med, Dept Med, Aurora, CO 80045 USA
[3] Univ Colorado, Sch Med, Dept Pharmacol, Aurora, CO 80045 USA
基金
瑞典研究理事会;
关键词
TRAIL; pro-apoptotic receptor agonists; apoptosis; TRAIL resistance; clinical trials; APOPTOSIS-INDUCING LIGAND; X-LINKED INHIBITOR; AGONISTIC MONOCLONAL-ANTIBODY; RECOMBINANT HUMAN APO2L/TRAIL; DEATH RECEPTOR 5; MEDIATED APOPTOSIS; CARCINOMA-CELLS; PHASE-I; PROTEASOME INHIBITION; SIX1; OVEREXPRESSION;
D O I
10.1038/onc.2012.164
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) and agonistic antibodies against TRAIL death receptors (DR) kill tumor cells while causing virtually no damage to normal cells. Several novel drugs targeting TRAIL receptors are currently in clinical trials. However, TRAIL resistance is a common obstacle in TRAIL-based therapy and limits the efficiency of these drugs. In this review article we discuss different mechanisms of TRAIL resistance, and how they can be predicted and therapeutically circumvented. In addition, we provide a brief overview of all TRAIL-based clinical trials conducted so far. It is apparent that although the effects of TRAIL therapy are disappointingly modest overall, a small subset of patients responds very well to TRAIL. We argue that the true potential of targeting TRAIL DRs in cancer can only be reached when we find efficient ways to select for those patients that are most likely to benefit from the treatment. To achieve this, it is crucial to identify biomarkers that can help us predict TRAIL sensitivity. Oncogene (2013) 32, 1341-1350; doi:10.1038/onc.2012.164; published online 14 May 2012
引用
收藏
页码:1341 / 1350
页数:10
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