Design, synthesis and biological evaluation of nuclear receptor-degradation inducers

被引:117
作者
Itoh, Yukihiro [1 ]
Kitaguchi, Risa [1 ]
Ishikawa, Minoru [1 ]
Naito, Mikihiko [2 ]
Hashimoto, Yuichi [1 ]
机构
[1] Univ Tokyo, Inst Mol & Cellular Biosci, Bunkyo Ku, Tokyo 1130032, Japan
[2] Natl Inst Hlth Sci, Setagaya Ku, Tokyo 1588501, Japan
基金
日本学术振兴会;
关键词
Protein knockdown; Protein degradation inducer; RAR; ER; AR; ACUTE PROMYELOCYTIC LEUKEMIA; TRANS-RETINOIC ACID; BULBAR MUSCULAR-ATROPHY; ANDROGEN RECEPTOR; PROSTATE-CANCER; BREAST-CANCER; RETINOBENZOIC ACIDS; BINDING PROTEINS; TAMOXIFEN RESISTANCE; CHIMERIC MOLECULES;
D O I
10.1016/j.bmc.2011.09.041
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Compounds that regulate the function(s) of nuclear receptors (NRs) are useful for biological studies and as candidate therapeutic agents. Most such compounds are agonists or antagonists. On the other hand, we have developed specific protein degradation inducers, which we designated as SNIPERs (Specific and Nongenetic IAPs-dependent Protein ERasers), for selective degradation of target proteins. SNIPERs are hybrid molecules consisting of an appropriate ligand for the protein of interest, coupled to a ligand for inhibitor of apoptosis proteins (IAPs), which target the bound protein for polyubiquitination and proteasomal degradation. We considered that protein knockdown with SNIPERs would be a promising alternative approach for modulating NR function. In this study, we designed and synthesized degradation inducers targeting retinoic acid receptor (RAR), estrogen receptor (ER), and androgen receptor (AR). These newly synthesized RAR, ER, and AR SNIPERs, 9, 11, and 13, respectively, were confirmed to significantly reduce the levels of the corresponding NRs in live cells. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6768 / 6778
页数:11
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