The future of pediatric cancer and complex diseases: Aren't they all?

被引:0
|
作者
Chanock, Stephen
Yeager, Meredith
机构
[1] NCI, Pediat Oncol Branch, Sect Genom Variat, Ctr Adv Technol,Pediat Oncol Branch, Bethesda, MD 20892 USA
[2] NCI, Core Genotyping Facil, Bethesda, MD 20892 USA
[3] NCI, Div Canc Epidemiol & Genet, Bethesda, MD 20892 USA
[4] NCI, SAIC Frederisck, Core Genotyping Facil, Bethesda, MD USA
关键词
complex diseases; pediatric cancer; single nucleotide polymorphism;
D O I
10.1002/pbc.21115
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Over the past decade, the investigation of human genetics and disease has pursued both common and uncommon germ-line variation and shown that both can be associated with altered risk for cancer and its outcomes. This line of investigation has not only begun to generate markers for disease but also insights into the biological pathways that are altered in cancer. Already, there is emerging evidence that germ-line genetic variation can alter susceptibility to different types of cancers, including pediatric cancers. It is evident that common genetic variation has emerged as a key component of a comprehensive understanding of pediatric cancer and its outcome. Future studies should unravel the complex interaction between genes and the environment. Pediatr Blood Cancer 2007;48:719-722. (c) 2007 Wiley-Liss, Inc.
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页码:719 / 722
页数:4
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