Targeting RNA modifications with pharmacological agents: New frontiers in cancer therapy

被引:3
作者
Guan, Angel [1 ,2 ]
Wong, Justin J. -L. [1 ,2 ,3 ]
机构
[1] Univ Sydney, Charles Perkins Ctr, Epigenet & RNA Biol Lab, Camperdown, Australia
[2] Univ Sydney, Fac Med & Hlth, Camperdown, Australia
[3] Univ Sydney, Charles Perkins Ctr, Bldg D17, Camperdown 2050, Australia
基金
英国医学研究理事会; 澳大利亚研究理事会;
关键词
cancer; cancer therapy; chemoresistance; N6-methyladenosine (m6A); RNA modification; METHYLTRANSFERASE METTL3 PROMOTES; CELL SELF-RENEWAL; DEMETHYLASE FTO INHIBITORS; STEM-LIKE CELLS; MESSENGER-RNA; BREAST-CANCER; NUCLEAR-RNA; M(6)A RNA; FAT MASS; N-6-METHYLADENOSINE M(6)A;
D O I
10.1002/cam4.6989
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The N6-methyladenosine (m6A) RNA modification has gained significant prominence as a new layer of regulatory mechanism that governs gene expression. Over the past decade, various m6A regulators responsible for introducing, eliminating, and recognising RNA methylation have been identified. Notably, these m6A regulators often exhibit altered expression patterns in cancer, occasionally offering prognostic value. Nonetheless, the complex roles of these regulators in human cancer pathology remain enigmatic, with conflicting outcomes reported in different studies.In recent years, a multitude of inhibitors and activators targeting m6A regulators have been reported. Several of these compounds have demonstrated promising efficacy in both in vitro and in vivo cancer models. These findings collectively underscore the dynamic landscape of m6A regulation in cancer biology, revealing its potential as a therapeutic target and prognostic indicator.
引用
收藏
页数:30
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