尼古丁
肺
DNA损伤
DNA修复
肺癌
致癌物
化学
药理学
DNA
医学
癌症研究
生物
病理
生物化学
内科学
作者
Hyun‐Wook Lee,Sung‐Hyun Park,Mao-wen Weng,Hsiang‐Tsui Wang,William C. Huang,Herbert Lepor,Xue‐Ru Wu,Lung‐Chi Chen,Moon-shong Tang
标识
DOI:10.1073/pnas.1718185115
摘要
Significance E-cigarette smoke (ECS) delivers nicotine through aerosols without burning tobacco. ECS is promoted as noncarcinogenic. We found that ECS induces DNA damage in mouse lung, bladder, and heart and reduces DNA-repair functions and proteins in lung. Nicotine and its nitrosation product 4-(methylnitrosamine)-1-(3-pyridyl)-1-butanone can cause the same effects as ECS and enhance mutations and tumorigenic cell transformation in cultured human lung and bladder cells. These results indicate that nicotine nitrosation occurs in the lung, bladder, and heart, and that its products are further metabolized into DNA damaging agents. We propose that ECS, through damaging DNA and inhibiting DNA repair, might contribute to human lung and bladder cancer as well as to heart disease, although further studies are required to substantiate this proposal.
科研通智能强力驱动
Strongly Powered by AbleSci AI