Huang Chaoqun, Chen Wei, Wang Xinxia
College of Animal Sciences, Zhejiang University, Hangzhou, Zhejiang 310058, China.
Key Laboratory of Molecular Animal Nutrition, Zhejiang University, Ministry of Education, Hangzhou, Zhejiang 310058, China.
Genes Dis. 2022 May 6;10(6):2351-2365. doi: 10.1016/j.gendis.2022.04.014. eCollection 2023 Nov.
Obesity has become a major health crisis in the past ∼50 years. The fat mass and obesity-associated (FTO) gene, identified by genome-wide association studies (GWAS), was first reported to be positively associated with obesity in humans. Mice with more copies of the FTO gene were observed to be obese, while loss of the gene in mice was found to protect from obesity. Later, FTO was found to encode an mA RNA demethylase and has a profound effect on many biological and metabolic processes. In this review, we first summarize recent studies that demonstrate the critical roles and regulatory mechanisms of FTO in obesity and metabolic disease. Second, we discuss the ongoing debates concerning the association between FTO polymorphisms and obesity. Third, since several small molecule drugs and micronutrients have been found to regulate metabolic homeostasis through controlling the expression or activity of FTO, we highlight the broad potential of targeting FTO for obesity treatment. Improving our understanding of FTO and the underlying mechanisms may provide new approaches for treating obesity and metabolic diseases.
在过去约50年里,肥胖已成为一个主要的健康危机。通过全基因组关联研究(GWAS)确定的脂肪量与肥胖相关(FTO)基因,首次被报道与人类肥胖呈正相关。观察到具有更多FTO基因拷贝的小鼠会肥胖,而在小鼠中该基因缺失则可预防肥胖。后来,发现FTO编码一种mRNA去甲基化酶,并对许多生物学和代谢过程产生深远影响。在这篇综述中,我们首先总结了近期表明FTO在肥胖和代谢疾病中的关键作用及调控机制的研究。其次,我们讨论了关于FTO多态性与肥胖之间关联的持续争论。第三,由于已发现几种小分子药物和微量营养素可通过控制FTO的表达或活性来调节代谢稳态,我们强调了靶向FTO治疗肥胖的广阔潜力。增进我们对FTO及其潜在机制的理解可能为治疗肥胖和代谢疾病提供新方法。