Greenwald Peter, Dunn Barbara K
Division of Cancer Prevention, National Cancer Institute, NIH, Bethesda, Maryland, USA.
Cancer Res. 2009 Mar 15;69(6):2151-62. doi: 10.1158/0008-5472.CAN-09-0416. Epub 2009 Mar 10.
The application of epidemiology to cancer prevention is relatively new, although observations of the potential causes of cancer have been reported for more than 2,000 years. Cancer was generally considered incurable until the late 19th century. Only with a refined understanding of the nature of cancer and strategies for cancer treatment could a systematic approach to cancer prevention emerge. The 20th century saw the elucidation of clues to cancer causation from observed associations with population exposures to tobacco, diet, environmental chemicals, and other exogenous factors. With repeated confirmation of such associations, researchers entertained for the first time the possibility that cancer, like many of the infectious diseases of the time, might be prevented. By the mid-20th century, with antibiotics successfully addressing the majority of infectious diseases and high blood pressure treatment beginning to affect the prevalence of heart disease in a favorable direction, the focus of much of epidemiology shifted to cancer. The early emphasis was on exploring, in greater depth, the environmental, dietary, hormonal, and other exogenous exposures for their potential associations with increased cancer risk. The first major breakthrough in identifying a modifiable cancer risk factor was the documentation of an association between tobacco smoking and lung cancer. During the past four decades, epidemiologic studies have generated population data identifying risk factors for cancers at almost every body site, with many cancers having multiple risk factors. The development of technologies to identify biological molecules has facilitated the incorporation of these molecular manifestations of biological variation into epidemiologic studies, as markers of exposure as well as putative surrogate markers of cancer outcome. This technological trend has, during the past two decades, culminated in emphasis on the identification of genetic variants and their products as correlates of cancer risk, in turn, creating opportunities to incorporate the discipline of molecular/genetic epidemiology into the study of cancer prevention. Epidemiology will undoubtedly continue contributing to cancer prevention by using traditional epidemiologic study designs to address broad candidate areas of interest, with molecular/genetic epidemiology investigations honing in on promising areas to identify specific factors that can be modified with the goal of reducing risk.
流行病学在癌症预防中的应用相对较新,尽管关于癌症潜在病因的观察报告已有2000多年的历史。直到19世纪后期,癌症通常还被认为是无法治愈的。只有在对癌症本质和癌症治疗策略有了更深入的理解之后,才出现了系统的癌症预防方法。20世纪,通过观察与人群接触烟草、饮食、环境化学物质和其他外源性因素之间的关联,人们阐明了癌症病因的线索。随着这些关联的反复证实,研究人员首次开始考虑癌症像当时许多传染病一样有可能被预防。到20世纪中叶,随着抗生素成功地解决了大多数传染病,高血压治疗开始朝着有利于降低心脏病患病率的方向发展,流行病学的大部分重点转移到了癌症上。早期的重点是更深入地探索环境、饮食、激素和其他外源性暴露与癌症风险增加之间的潜在关联。确定一个可改变的癌症风险因素的第一个重大突破是记录了吸烟与肺癌之间的关联。在过去的四十年里,流行病学研究产生了大量人群数据,确定了几乎每个身体部位癌症的风险因素,许多癌症有多个风险因素。识别生物分子的技术发展促进了将这些生物变异的分子表现纳入流行病学研究,作为暴露的标志物以及癌症结局的假定替代标志物。在过去的二十年里,这种技术趋势最终导致重点转向识别基因变异及其产物作为癌症风险的相关因素,进而为将分子/基因流行病学学科纳入癌症预防研究创造了机会。流行病学无疑将继续通过使用传统的流行病学研究设计来关注广泛的感兴趣的候选领域,为癌症预防做出贡献,而分子/基因流行病学研究则专注于有前景的领域,以识别可以改变的特定因素,目标是降低风险。