Stracquadanio Giovanni, Wang Xuting, Wallace Marsha D, Grawenda Anna M, Zhang Ping, Hewitt Juliet, Zeron-Medina Jorge, Castro-Giner Francesc, Tomlinson Ian P, Goding Colin R, Cygan Kamil J, Fairbrother William G, Thomas Laurent F, Sætrom Pål, Gemignani Federica, Landi Stefano, Schuster-Böckler Benjamin, Bell Douglas A, Bond Gareth L
Ludwig Institute for Cancer Research, University of Oxford, Nuffield Department of Clinical Medicine, Old Road Campus Research Building, Oxford OX3 7DQ, UK.
Environmental Genomics Group, Genome Integrity and Structural Biology, National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, North Carolina 27709, USA.
Nat Rev Cancer. 2016 Apr;16(4):251-65. doi: 10.1038/nrc.2016.15.
Decades of research have shown that mutations in the p53 stress response pathway affect the incidence of diverse cancers more than mutations in other pathways. However, most evidence is limited to somatic mutations and rare inherited mutations. Using newly abundant genomic data, we demonstrate that commonly inherited genetic variants in the p53 pathway also affect the incidence of a broad range of cancers more than variants in other pathways. The cancer-associated single nucleotide polymorphisms (SNPs) of the p53 pathway have strikingly similar genetic characteristics to well-studied p53 pathway cancer-causing somatic mutations. Our results enable insights into p53-mediated tumour suppression in humans and into p53 pathway-based cancer surveillance and treatment strategies.
数十年的研究表明,与其他信号通路中的突变相比,p53应激反应信号通路中的突变对多种癌症发病率的影响更大。然而,大多数证据仅限于体细胞突变和罕见的遗传突变。利用新近大量出现的基因组数据,我们证明,与其他信号通路中的变异相比,p53信号通路中常见的遗传变异对多种癌症发病率的影响也更大。p53信号通路中与癌症相关的单核苷酸多态性(SNP)与经过充分研究的p53信号通路致癌体细胞突变具有惊人相似的遗传特征。我们的研究结果有助于深入了解p53介导的人类肿瘤抑制作用以及基于p53信号通路的癌症监测和治疗策略。