烟草烟雾
遗传学
癌症
生物
烟草使用
医学
计算生物学
环境卫生
人口
作者
Ludmil B. Alexandrov,Young Seok Ju,Kerstin Haase,Peter Van Loo,Sancha Martin,Serena Nik‐Zainal,Yasushi Totoki,Akihiro Fujimoto,Hidewaki Nakagawa,Tatsuhiro Shibata,Peter J. Campbell,Paolo Vineis,David H. Phillips,Michael R. Stratton
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2016-11-03
卷期号:354 (6312): 618-622
被引量:1105
标识
DOI:10.1126/science.aag0299
摘要
Tobacco smoking increases the risk of at least 17 classes of human cancer. We analyzed somatic mutations and DNA methylation in 5243 cancers of types for which tobacco smoking confers an elevated risk. Smoking is associated with increased mutation burdens of multiple distinct mutational signatures, which contribute to different extents in different cancers. One of these signatures, mainly found in cancers derived from tissues directly exposed to tobacco smoke, is attributable to misreplication of DNA damage caused by tobacco carcinogens. Others likely reflect indirect activation of DNA editing by APOBEC cytidine deaminases and of an endogenous clocklike mutational process. Smoking is associated with limited differences in methylation. The results are consistent with the proposition that smoking increases cancer risk by increasing the somatic mutation load, although direct evidence for this mechanism is lacking in some smoking-related cancer types.
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