Hursting Stephen D, Lashinger Laura M, Colbert Lisa H, Rogers Connie J, Wheatley Karrie W, Nunez Nomeli P, Mahabir Somdat, Barrett J Carl, Forman Michele R, Perkins Susan N
Division of Nutritional Sciences, University of Texas, Austin, TX 78712, USA.
Curr Cancer Drug Targets. 2007 Aug;7(5):484-91. doi: 10.2174/156800907781386623.
The prevalence of obesity, an established epidemiologic risk factor for many cancers, has risen steadily for the past several decades in the U.S. Particularly alarming are the increasing rates of obesity among children, portending continuing increases in the rates of obesity and obesity-related cancers for many years to come. Unfortunately, the mechanisms underlying the association between obesity and cancer are not well understood. In particular, the effects and mechanistic targets of interventions that modulate energy balance, such as reduced calorie diets and physical activity, on the carcinogenesis process have not been well characterized. The purpose of this review is to provide a strong foundation for future mechanistic-based research in this area by describing key animal and human studies of energy balance modulations involving diet, exercise, or pharmaceutical agents and by focusing on the interrelated pathways affected by alterations in energy balance. Particular attention in this review is placed on the components of the insulin/IGF-1/Akt pathway, which has emerged as a predominant target for disrupting the obesity-cancer link. Also discussed is the promise of global approaches, including genomics, proteomics, and metabolomics, for the elucidation of energy balance-responsive pathways. The ultimate goal of this work is to provide the missing mechanistic information necessary to identify targets for the prevention and control of cancers related to or caused by excess body weight.
肥胖是许多癌症公认的流行病学危险因素,在过去几十年里,美国肥胖症的患病率一直在稳步上升。尤其令人担忧的是儿童肥胖率不断上升,这预示着未来许多年肥胖症及与肥胖相关癌症的发病率将持续上升。不幸的是,肥胖与癌症之间关联的潜在机制尚未得到充分理解。特别是,调节能量平衡的干预措施,如减少热量摄入的饮食和体育活动,对致癌过程的影响和作用机制靶点尚未得到很好的描述。本综述的目的是通过描述涉及饮食、运动或药物制剂的能量平衡调节的关键动物和人体研究,并关注受能量平衡改变影响的相互关联途径,为该领域未来基于机制的研究提供坚实基础。本综述特别关注胰岛素/IGF-1/Akt途径的组成部分,该途径已成为破坏肥胖与癌症联系的主要靶点。还讨论了包括基因组学、蛋白质组学和代谢组学在内的全局方法在阐明能量平衡响应途径方面的前景。这项工作的最终目标是提供缺失的机制信息,以确定预防和控制与超重相关或由超重引起的癌症的靶点。