Small molecules targeting microRNAs: new opportunities and challenges in precision cancer therapy

被引:2
|
作者
Jurj, Ancuta [1 ]
Fontana, Beatrice [1 ,2 ]
Varani, Gabriele [3 ]
Calin, George A. [1 ,4 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Translat Mol Pathol, Houston, TX 77054 USA
[2] Alma Mater Studiorum Univ Bologna, Dept Med & Surg Sci DIMEC, Bologna, Italy
[3] Univ Washington, Dept Chem, Seattle, WA 98195 USA
[4] Univ Texas MD Anderson Canc Ctr, Ctr RNA Interference & Noncoding RNAs, Houston, TX 77030 USA
关键词
NONCODING RNAS; ONCOGENIC MICRORNAS; MIRNA ASSOCIATIONS; TAR RNA; DESIGN; INHIBITORS; EXPRESSION; DISCOVERY; IDENTIFICATION; BIOGENESIS;
D O I
10.1016/j.trecan.2024.06.006
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Noncoding RNAs, especially miRNAs, play a pivotal role in cancer initiation and metastasis, underscoring their susceptibility to precise modulation via small molecule inhibitors. This review examines the innovative strategy of targeting oncogenic miRNAs with small drug-like molecules, an approach that can reshape the cancer treatment landscape. We review the current understanding of the multifaceted roles of miRNAs in oncogenesis, highlighting emerging therapeutic paradigms that have the potential to expand cancer treatment options. As research on small molecule inhibitors of miRNA is still in its early stages, ongoing investigative efforts and the development of new technologies and chemical matter are essential to fulfill the significant potential of this innovative approach to cancer treatment.
引用
收藏
页码:809 / 824
页数:16
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