Alexandrov Ludmil B, Ju Young Seok, Haase Kerstin, Van Loo Peter, Martincorena Iñigo, Nik-Zainal Serena, Totoki Yasushi, Fujimoto Akihiro, Nakagawa Hidewaki, Shibata Tatsuhiro, Campbell Peter J, Vineis Paolo, Phillips David H, Stratton Michael R
Theoretical Biology and Biophysics (T-6), Los Alamos National Laboratory, Los Alamos, NM 87545, USA.
Center for Nonlinear Studies, Los Alamos National Laboratory, Los Alamos, NM 87545, USA.
Science. 2016 Nov 4;354(6312):618-622. doi: 10.1126/science.aag0299.
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.
吸烟会增加至少17种人类癌症的风险。我们分析了5243例因吸烟而风险升高的癌症类型中的体细胞突变和DNA甲基化情况。吸烟与多种不同突变特征的突变负担增加有关,这些突变特征在不同癌症中的贡献程度不同。其中一种特征主要见于源自直接接触烟草烟雾组织的癌症,它归因于烟草致癌物导致的DNA损伤的错误复制。其他特征可能反映了APOBEC胞苷脱氨酶对DNA编辑的间接激活以及一种内源性时钟样突变过程。吸烟与甲基化方面的有限差异有关。这些结果与吸烟通过增加体细胞突变负荷来增加癌症风险这一观点一致,尽管在某些与吸烟相关的癌症类型中缺乏这一机制的直接证据。