Cyclic Peptidomimetics as Inhibitor for miR-155 Biogenesis

被引:21
|
作者
Yan, Hao [1 ]
Zhou, Mi [2 ]
Bhattarai, Umesh [1 ]
Song, Yabin [1 ]
Zheng, Mengmeng [2 ]
Cai, Jianfeng [2 ]
Liang, Fu-Sen [1 ,3 ]
机构
[1] Univ New Mexico, Dept Chem & Chem Biol, 300 Terrace St NE, Albuquerque, NM 87131 USA
[2] Univ S Florida, Dept Chem, 4202 E Fowler Ave, Tampa, FL 33620 USA
[3] Case Western Reserve Univ, Dept Chem, Cleveland, OH 44106 USA
基金
美国国家卫生研究院;
关键词
peptidomimetics; combinatorial chemistry; microRNA; inhibitor; antitumor agents; SMALL-MOLECULE INHIBITORS; TARGETING RNA; MIR-21; AMINOGLYCOSIDES; EXPRESSION; MICRORNAS; DISCOVERY; APOPTOSIS; PRECURSOR; SEQUENCE;
D O I
10.1021/acs.molpharmaceut.8b01247
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
miR-155 plays key promoting roles in several cancers and emerges as an important anticancer therapeutic target. However, the discovery of small molecules that target RNAs is challenging. Peptidomimetics have been shown to be a rich source for discovering novel ligands to regulate cellular proteins. However, the potential of using peptidomimetics for RNA targeting is relatively unexplored. To this end, we designed and synthesized members of a novel 320 000 compound macrocyclic peptidomimetic library. An affinity-based screening protocol led to the identification of a pre-miR-155 binder that inhibits oncogenic miR-155 maturation in vitro and in cell and induces cancer cell apoptosis. The results of this investigation demonstrate that macrocyclic peptidomimetics could serve as a new scaffold for RNA targeting.
引用
收藏
页码:914 / 920
页数:7
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