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TRAIL receptor-targeted therapeutics: Resistance mechanisms and strategies to avoid them

期刊

DRUG RESISTANCE UPDATES
卷 11, 期 1-2, 页码 17-24

出版社

CHURCHILL LIVINGSTONE
DOI: 10.1016/j.drup.2008.02.001

关键词

TRAIL; DR4; DR5; apoptosis; Six1; GALNT14; XIAP; mapatumumab; resistance; cancer

资金

  1. NCI NIH HHS [P30 CA046934, R01 CA111421-04, R01 CA111421] Funding Source: Medline

向作者/读者索取更多资源

Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) receptors are attractive therapeutic targets in cancer because agents that activate these receptors directly induce tumor cell apoptosis and have low toxicity to normal tissues. Consequently, several different drugs that target these receptors (recombinant TRAIL and various agonistic antibodies that activate one of the two TRAIL receptors) have been developed and are being tested in human clinical trials. However, in vitro and in vivo data suggest that resistance to these agents may limit their clinical effectiveness. In this review, we discuss recent findings about some of the ways these resistance mechanisms arise, potential biomarkers to identify TRAIL resistance in patients (Six1, GALNT14, XIAP, certain microRNAs) and potential ways to circumvent resistance and resensitize tumors. (C) 2008 Elsevier Ltd. All rights reserved.

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