Chrysotile asbestos fibers mediate homologous recombination in Rat2 lambda fibroblasts: Implications for carcinogenesis

被引:17
作者
LezonGeyda, K
Jaime, CM
Godbold, JH
Savransky, EF
Hope, A
Kheiri, SA
Dzmura, ZM
Uehara, H
Johnson, EM
Fasy, TM
机构
[1] CUNY MT SINAI SCH MED, DEPT COMMUNITY MED, NEW YORK, NY 10029 USA
[2] CUNY MT SINAI SCH MED, CTR ENVIRONM HLTH SCI, NEW YORK, NY 10029 USA
[3] CUNY MT SINAI SCH MED, BROOKDALE CTR MOL BIOL, NEW YORK, NY 10029 USA
来源
MUTATION RESEARCH-ENVIRONMENTAL MUTAGENESIS AND RELATED SUBJECTS | 1996年 / 361卷 / 2-3期
关键词
chrysotile asbestos; lacI; homologous recombination; Rat2 lambda cell;
D O I
10.1016/S0165-1161(96)90245-9
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Asbestos fibers are widespread environmental carcinogens whose mutagenicity is now established. Nonetheless, the molecular nature of these mutations and the mechanisms by which they accelerate carcinogenesis remain poorly understood. We have assessed the ability of asbestos fibers to promote homologous recombination, a potent mechanism for generating intrachromosomal rearrangements, such as deletions, and mitotic recombination. For this, we have developed a new assay which determines the extent to which a marker gene present in DNA introduced by asbestos can recombine with homologous genes residing in a transfected cell. We have demonstrated that Calidria chrysotile fibers are mutagenic and are able to mediate transfection of molecularly marked mutant lacI genes in a manner that results in their preferential recombination with homologous wild-type genes in the transfected cell. Asbestos induced recombination events may play a significant role in asbestos mutagenesis and carcinogenesis, and promotion of recombination may underlie the well-recognized synergy of asbestos with other carcinogens.
引用
收藏
页码:113 / 120
页数:8
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