Chemical Knockdown of MicroRNA with Small-Molecule Chimeras

被引:1
作者
Feng, Yi [1 ]
Li, Jinbo [1 ]
Zhang, Yan [1 ]
机构
[1] Nanjing Univ, State Key Lab Analyt Chem Life Sci, Jiangsu Key Lab Adv Organ Mat, Sch Chem & Chem Engn,Chem & Biomed Innovat Ctr, Nanjing 210023, Peoples R China
基金
中国国家自然科学基金;
关键词
cancer therapy; microRNA; small-molecule binders; small-molecule chimeras; targeted degradation; SEQUENCE-BASED DESIGN; RNA; TARGET; RECOGNITION; CANCER; THERAPEUTICS; INHIBITION; CLEAVAGE;
D O I
10.1002/cbic.202000287
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
This concept article introduces the emerging area of small-molecule chimeras (SMCs) for knocking down microRNAs (miRNAs), which are endogenous gene silencers involved in diverse pathological processes. Compared with agents for genetic knockdown, small-molecules hold significant promise in this field due to their ideal pharmacokinetic and pharmacodynamic properties. The SMCs introduced here are hetero-bifunctional molecules comprising small-molecule binders (SMBs) of miRNAs and chemical functionalities that either directly cleave RNAs or recruit ribonucleases to destroy RNAs. Binding of SMBs to miRNAs brings SMCs' chemical functionalities close to the miRNA, eventually causing miRNA degradation. Compared with parent SMBs, SMCs exhibit remarkably enhanced potency and specificity in miRNA inhibition. The development and application of SMCs for miRNAs will be discussed.
引用
收藏
页码:3180 / 3185
页数:6
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