Reznik Robert, Hendifar Andrew E, Tuli Richard
Department of Radiation Oncology, Cedars-Sinai Medical Center Los Angeles, CA, USA.
Front Physiol. 2014 Mar 3;5:87. doi: 10.3389/fphys.2014.00087. eCollection 2014.
Pancreatic ductal adenocarcinoma (PDAC) is the fourth leading cause of cancer deaths in both men and women in the United States, carrying a 5-year survival rate of approximately 5%, which is the poorest prognosis of any solid tumor type. Given the dismal prognosis associated with PDAC, a more thorough understanding of risk factors and genetic predisposition has important implications not only for cancer prevention, but also for screening techniques and the development of personalized therapies. While screening of the general population is not recommended or practicable with current diagnostic methods, studies are ongoing to evaluate its usefulness in people with at least 5- to 10-fold increased risk of PDAC. In order to help identify high-risk populations who would be most likely to benefit from early detection screening tests for pancreatic cancer, discovery of additional pancreatic cancer susceptibility genes is crucial. Thus, specific gene-based, gene-product, and marker-based testing for the early detection of pancreatic cancer are currently being developed, with the potential for these to be useful as potential therapeutic targets as well. The goal of this review is to provide an overview of the genetic basis for PDAC with a focus on germline and familial determinants. A discussion of potential therapeutic targets and future directions in screening and treatment is also provided.
胰腺导管腺癌(PDAC)是美国男性和女性癌症死亡的第四大主要原因,其5年生存率约为5%,是所有实体瘤类型中预后最差的。鉴于与PDAC相关的预后不佳,更全面地了解风险因素和遗传易感性不仅对癌症预防具有重要意义,而且对筛查技术和个性化治疗的发展也具有重要意义。虽然目前的诊断方法不建议或不适用于对普通人群进行筛查,但正在进行研究以评估其对胰腺癌风险至少增加5至10倍的人群的有效性。为了帮助识别最有可能从胰腺癌早期检测筛查试验中受益的高危人群,发现更多的胰腺癌易感基因至关重要。因此,目前正在开发基于特定基因、基因产物和标志物的胰腺癌早期检测测试,这些测试也有可能作为潜在的治疗靶点。本综述的目的是概述PDAC的遗传基础,重点是种系和家族决定因素。还讨论了潜在的治疗靶点以及筛查和治疗的未来方向。