An evolutionary perspective on field cancerization

被引:322
作者
Curtius, Kit [1 ]
Wright, Nicholas A. [1 ]
Graham, Trevor A. [1 ]
机构
[1] Barts Canc Inst, Ctr Tumour Biol, London EC1M 6BQ, England
基金
英国惠康基金;
关键词
HIGH-GRADE DYSPLASIA; INFLAMMATORY-BOWEL-DISEASE; SQUAMOUS-CELL CARCINOMA; BARRETTS-ESOPHAGUS; ULCERATIVE-COLITIS; STEM-CELLS; IN-SITU; DNA METHYLATION; CANCER-RISK; LUNG-CANCER;
D O I
10.1038/nrc.2017.102
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Tumorigenesis begins long before the growth of a clinically detectable lesion and, indeed, even before any of the usual morphological correlates of pre-malignancy are recognizable. Field cancerization, which is the replacement of the normal cell population by a cancer-primed cell population that may show no morphological change, is now recognized to underlie the development of many types of cancer, including the common carcinomas of the lung, colon, skin, prostate and bladder. Field cancerization is the consequence of the evolution of somatic cells in the body that results in cells that carry some but not all phenotypes required for malignancy. Here, we review the evidence of field cancerization across organs and examine the biological mechanisms that drive the evolutionary process that results in field creation. We discuss the clinical implications, principally, how measurements of the cancerized field could improve cancer risk prediction in patients with pre-malignant disease.
引用
收藏
页码:19 / 32
页数:14
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