Genotoxicity of tobacco smoke and tobacco smoke condensate: a review

被引:383
作者
DeMarini, DM [1 ]
机构
[1] US EPA, Div Environm Carcinogenesis, Natl Hlth & Environm Effects Res Lab, Res Triangle Pk, NC 27711 USA
关键词
cigarette smoke; mutagenicity; lung cancer; complex mixture; tobacco smoke;
D O I
10.1016/j.mrrev.2004.02.001
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
This report reviews the literature on the genotoxicity of mainstream tobacco smoke and cigarette smoke condensate (CSC) published since 1985. CSC is genotoxic in nearly all systems in which it has been tested, with the base/neutral fractions being the most mutagenic. In rodents, cigarette smoke induces sister chromatid exchanges (SCEs) and micronuclei in bone marrow and lung cells. In humans, newborns of smoking mothers have elevated frequencies of HPRT mutants, translocations, and DNA strand breaks. Sperm of smokers have elevated frequencies of aneuploidy, DNA adducts, strand breaks, and oxidative damage. Smoking also produces mutagenic cervical mucus, micronuclei in cervical epithelial cells, and genotoxic amniotic fluid. These data suggest that tobacco smoke may be a human germ-cell mutagen. Tobacco smoke produces mutagenic urine, and it is a human somatic-cell mutagen, producing HPRT mutations, SCEs, microsatellite instability, and DNA damage in a variety of tissues. Of the 11 organ sites at which smoking causes cancer in humans, smoking-associated genotoxic effects have been found in all eight that have been examined thus far: oral/nasal, esophagus, pharynx/larynx, lung, pancreas, myeoloid organs, bladder/ureter, uterine cervix. Lung tumors of smokers contain a high frequency and unique spectrum of TP53 and KPAS mutations, reflective of the PAH (and possibly other) compounds in the smoke. Further studies are needed to clarify the modulation of the genotoxicity of tobacco smoke by various genetic polymorphisms. These data support a model of tobacco smoke carcinogenesis in which the components of tobacco smoke induce mutations that accumulate in a field of tissue that, through selection, drive the carcinogenic process. Most of the data reviewed here are from studies of human smokers. Thus, their relevance to humans cannot be denied, and their explanatory powers not easily dismissed. Tobacco smoke is now the most extreme example of a systemic human mutagen. Published by Elsevier B.V.
引用
收藏
页码:447 / 474
页数:28
相关论文
共 399 条
[11]  
Anderson D, 1997, ENVIRON MOL MUTAGEN, V30, P205, DOI 10.1002/(SICI)1098-2280(1997)30:2<205::AID-EM13>3.0.CO
[12]  
2-H
[13]   CYTOGENETIC EFFECTS IN A GROUP OF TRAFFIC POLICEMEN IN CAIRO [J].
ANWAR, WA ;
KAMAL, AAM .
MUTATION RESEARCH, 1988, 208 (3-4) :225-231
[14]  
AOSHIBA K, 2001, AM J PHYSIOL-LUNG C, V281, P1401
[15]  
Asami S, 1996, CANCER RES, V56, P2546
[16]   Cigarette smoking induces an increase in oxidative DNA damage, 8-hydroxydeoxyguanosine, in a central site of the human lung [J].
Asami, S ;
Manabe, H ;
Miyake, J ;
Tsurudome, Y ;
Hirano, T ;
Yamaguchi, R ;
Itoh, H ;
Kasai, H .
CARCINOGENESIS, 1997, 18 (09) :1763-1766
[17]   MUTAGENICITY OF WOOD SMOKE CONDENSATES IN THE SALMONELLA MICROSOME ASSAY [J].
ASITA, AO ;
MATSUI, M ;
NOHMI, T ;
MATSUOKA, A ;
HAYASHI, M ;
ISHIDATE, M ;
SOFUNI, T ;
KOYANO, M ;
MATSUSHITA, H .
MUTATION RESEARCH, 1991, 264 (01) :7-14
[18]   FACTORS CONTRIBUTING TO CHROMOSOME-DAMAGE IN LYMPHOCYTES OF CIGARETTE SMOKERS [J].
AU, WW ;
WALKER, DM ;
WARD, JB ;
WHORTON, E ;
LEGATOR, MS ;
SINGH, V .
MUTATION RESEARCH, 1991, 260 (02) :137-144
[19]   MUTAGENICITY OF THE FRACTIONATED ORGANIC EMISSIONS FROM DIESEL, CIGARETTE-SMOKE CONDENSATE, COKE-OVEN, AND ROOFING TAR IN THE AMES ASSAY [J].
AUSTIN, AC ;
CLAXTON, LD ;
LEWTAS, J .
ENVIRONMENTAL MUTAGENESIS, 1985, 7 (04) :471-487
[20]  
AUTRUP H, 2000, MUTAT RES, P464