Is miR therapeutic targeting still a miRage?

被引:7
作者
Levantini, Elena [1 ,2 ,3 ,4 ]
机构
[1] Harvard Med Sch, Boston, MA 02115 USA
[2] Beth Israel Deaconess Med Ctr, Boston, MA 02215 USA
[3] Harvard Stem Cell Inst, Cambridge, MA 02138 USA
[4] Natl Res Council CNR, Inst Biomed Technol, Area Ric Pisa, I-56124 Pisa, Italy
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2021年 / 26卷 / 10期
关键词
RNA therapeutics; Biomarkers; miR-21; NSCLC; Cancer; CELL LUNG-CANCER; HUMAN MICRORNA GENES; TUMOR-SUPPRESSOR; DOWN-REGULATION; GASTRIC-CANCER; LINKING INFLAMMATION; CURRENT STRATEGIES; NONCODING RNAS; MESSENGER-RNAS; EXPRESSION;
D O I
10.52586/4979
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
Since the discovery of the first microRNA (miR), almost three decades ago, the roles played by miRs under normal and diseased settings have been widely investigated. miRs are found to play crucial roles in cancer initiation and progression, as well as towards therapy response mechanisms. Therefore, they are relevant and attractive targets for therapeutic development. Many preclinical studies have demonstrated their promise as future anti-cancer tools. Recently, increasing number of early phase clinical trials have emerged. In this Commentary, we will summarize the major discoveries within the miR research field and highlight the status quo of current miR-therapeutics, which has prominent potential of impacting future cancer regimens given their massive dysregulation in oncogenic processes.
引用
收藏
页码:680 / 692
页数:13
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