Zuidhof Hidde R, Calkhoven Cornelis F
European Research Institute for the Biology of Ageing (ERIBA), University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
Cancer Res. 2022 Jun 15;82(12):2201-2212. doi: 10.1158/0008-5472.CAN-21-3710.
The epitranscriptome represents the more than 140 types of chemically varying and reversable RNA modifications affecting RNA fate. Among these, the most relevant for this review are the mRNA modifications N6-methyladenosine and N6,2'-O-dimethyladenosine. Epitranscriptomic mRNA biology involves RNA methyltransferases (so-called "writers"), RNA demethylases ("erasers"), and RNA-binding proteins ("readers") that interact with methylation sites to determine the functional outcome of the modification. In this review, we discuss the role of a specific RNA demethylase encoded by the fat mass and obesity-associated gene (FTO) in cancer. FTO initially became known as the strongest genetic link for human obesity. Only in 2010, 16 years after its discovery, was its enzymatic function as a demethylase clarified, and only recently has its role in the development of cancer been revealed. FTO functions are challenging to study and interpret because of its genome-wide effects on transcript turnover and translation. We review the discovery of FTO and its enzymatic function, the tumor-promoting and suppressive roles of FTO in selected cancer types, and its potential as a therapeutic target.
表观转录组代表了140多种影响RNA命运的化学可变且可逆的RNA修饰类型。其中,与本综述最相关的是mRNA修饰N6-甲基腺苷和N6,2'-O-二甲基腺苷。表观转录组学的mRNA生物学涉及与甲基化位点相互作用以确定修饰功能结果的RNA甲基转移酶(所谓的“书写者”)、RNA去甲基化酶(“擦除者”)和RNA结合蛋白(“阅读者”)。在本综述中,我们讨论了由脂肪量和肥胖相关基因(FTO)编码的一种特定RNA去甲基化酶在癌症中的作用。FTO最初作为人类肥胖最强的遗传关联而为人所知。直到2010年,也就是其发现16年后,其作为去甲基化酶的酶促功能才得以阐明,并且直到最近其在癌症发生发展中的作用才被揭示。由于FTO对转录本周转和翻译具有全基因组范围的影响,其功能研究和解读具有挑战性。我们综述了FTO的发现及其酶促功能、FTO在特定癌症类型中的促肿瘤和抑肿瘤作用以及其作为治疗靶点的潜力。