辐射暴露
切尔诺贝利核事故
甲状腺癌
甲状腺癌
癌变
人口
医学
生物
跨代表观遗传学
甲状腺
癌症
生理学
肿瘤科
遗传学
内科学
核医学
基因
环境卫生
表观遗传学
作者
Lindsay M. Morton,Danielle M. Karyadi,Chip Stewart,Bogdanova Ti,Eric T. Dawson,Mia Steinberg,Jieqiong Dai,Stephen W. Hartley,Sara J. Schonfeld,Joshua N. Sampson,Yosef E. Maruvka,Vidushi Kapoor,Dale A. Ramsden,Juan Carvajal-Garcia,Charles M. Perou,Joel S. Parker,Marko Krznarić,Meredith Yeager,Joseph F. Boland,Amy Hutchinson
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2021-04-22
卷期号:372 (6543)
被引量:159
标识
DOI:10.1126/science.abg2538
摘要
The 1986 Chernobyl nuclear power plant accident increased papillary thyroid carcinoma (PTC) incidence in surrounding regions, particularly for radioactive iodine (131I)-exposed children. We analyzed genomic, transcriptomic, and epigenomic characteristics of 440 PTCs from Ukraine (from 359 individuals with estimated childhood 131I exposure and 81 unexposed children born after 1986). PTCs displayed radiation dose-dependent enrichment of fusion drivers, nearly all in the mitogen-activated protein kinase pathway, and increases in small deletions and simple/balanced structural variants that were clonal and bore hallmarks of nonhomologous end-joining repair. Radiation-related genomic alterations were more pronounced for individuals who were younger at exposure. Transcriptomic and epigenomic features were strongly associated with driver events but not radiation dose. Our results point to DNA double-strand breaks as early carcinogenic events that subsequently enable PTC growth after environmental radiation exposure.
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