Jiangsu Key Laboratory of Drug Screening, China Pharmaceutical University, Nanjing, 210009, China.
Department of Epidemiology, School of Public Health, Nanjing Medical University, Nanjing, 211166, China.
Obes Rev. 2016 Sep;17(9):907-14. doi: 10.1111/obr.12430. Epub 2016 Jun 3.
Obesity has become epidemic worldwide, and abdominal obesity has a negative impact on health. Current treatment options on obesity, however, still remain limited. It is then of importance to find a new target for anti-obesity drug development based upon recent molecular studies in obesity. Adenylate cyclase 3 (ADCY3) is the third member of adenylyl cyclase family and catalyses the synthesis of cAMP from ATP. Genetic studies with candidate gene and genome-wide association study approaches have demonstrated that ADCY3 genetic polymorphisms are associated with obesity in European and Chinese populations. Epigenetic studies have indicated that increased DNA methylation levels in the ADCY3 gene are involved in the pathogenesis of obesity. Furthermore, biological analyses with animal models have implicated that ADCY3 dysfunction resulted in increased body weight and fat mass, while reduction of body weight is partially explained by ADCY3 activation. In this review, we describe genomic and biological features of ADCY3, summarize genetic and epigenetic association studies of the ADCY3 gene with obesity and discuss dysfunction and activation of ADCY3. Based upon all data, we suggest that ADCY3 is a new target for anti-obesity drug development. Further investigation on the effectiveness of ADCY3 activator and its delivery approach to treat abdominal obesity has been taken into our consideration.
肥胖已在全球流行,腹型肥胖对健康有负面影响。然而,目前的肥胖治疗选择仍然有限。因此,基于肥胖的最新分子研究,寻找新的抗肥胖药物靶点非常重要。腺苷酸环化酶 3(ADCY3)是腺苷酸环化酶家族的第三个成员,催化 ATP 生成 cAMP。候选基因和全基因组关联研究的遗传研究表明,ADCY3 基因多态性与欧洲和中国人群的肥胖有关。表观遗传研究表明,ADCY3 基因中 DNA 甲基化水平的增加与肥胖的发病机制有关。此外,动物模型的生物学分析表明,ADCY3 功能障碍导致体重和脂肪量增加,而体重减轻部分可以通过 ADCY3 激活来解释。在这篇综述中,我们描述了 ADCY3 的基因组和生物学特征,总结了 ADCY3 基因与肥胖的遗传和表观遗传关联研究,并讨论了 ADCY3 的功能障碍和激活。基于所有数据,我们认为 ADCY3 是开发抗肥胖药物的新靶点。我们已经考虑进一步研究 ADCY3 激活剂的有效性及其治疗腹型肥胖的输送方法。