Cheung Otto K-W, Cheng Alfred S-L
School of Biomedical Sciences, The Chinese University of Hong Kong Hong Kong, China.
School of Biomedical Sciences, The Chinese University of Hong Kong Hong Kong, China; State Key Laboratory of Digestive Disease, The Chinese University of Hong Kong Hong Kong, China.
Front Genet. 2016 Sep 20;7:168. doi: 10.3389/fgene.2016.00168. eCollection 2016.
Liver cancer is the third most common cancer type and the second leading cause of deaths in men. Large population studies have demonstrated remarkable gender disparities in the incidence and the cumulative risk of liver cancer. A number of emerging risk factors regarding metabolic alterations associated with obesity, diabetes and dyslipidemia have been ascribed to the progression of non-alcoholic fatty liver diseases (NAFLD) and ultimately liver cancer. The deregulation of fat metabolism derived from excessive insulin, glucose, and lipid promotes cancer-causing inflammatory signaling and oxidative stress, which eventually triggers the uncontrolled hepatocellular proliferation. This review presents the current standing on the gender differences in body fat compositions and their mechanistic linkage with the development of NAFLD-related liver cancer, with an emphasis on genetic, epigenetic and microRNA control. The potential roles of sex hormones in instructing adipocyte metabolic programs may help unravel the mechanisms underlying gender dimorphism in liver cancer and identify the metabolic targets for disease management.
肝癌是第三大常见癌症类型,也是男性第二大主要死因。大型人群研究表明,肝癌的发病率和累积风险存在显著的性别差异。一些与肥胖、糖尿病和血脂异常相关的代谢改变的新兴风险因素已被归因于非酒精性脂肪性肝病(NAFLD)的进展,并最终导致肝癌。由过量胰岛素、葡萄糖和脂质引起的脂肪代谢失调会促进致癌性炎症信号传导和氧化应激,最终引发肝细胞的失控增殖。本综述介绍了身体脂肪组成的性别差异及其与NAFLD相关肝癌发生的机制联系的现状,重点是遗传、表观遗传和微小RNA控制。性激素在指导脂肪细胞代谢程序中的潜在作用可能有助于揭示肝癌性别二态性的潜在机制,并确定疾病管理的代谢靶点。