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低剂量[D3]-甲基亚硝基脲暴露后培养的人细胞内源性和外源性O(6)-甲基-dG和N7-甲基-G加合物的分子剂量测定

Molecular dosimetry of endogenous and exogenous O(6)-methyl-dG and N7-methyl-G adducts following low dose [D3]-methylnitrosourea exposures in cultured human cells.

作者信息

Sharma Vyom, Collins Leonard B, Clement Jean M, Zhang Zhenfa, Nakamura Jun, Swenberg James A

机构信息

Department of Environmental Sciences and Engineering, University of North Carolina , Campus Box 7431, Chapel Hill, North Carolina 27599-7431, United States.

出版信息

Chem Res Toxicol. 2014 Apr 21;27(4):480-2. doi: 10.1021/tx5000602. Epub 2014 Mar 26.

Abstract

For DNA-reactive chemicals, a low dose linear assessment of cancer risk is the science policy default. In the present study, we quantitated the endogenous and exogenous N7-methyl-G and O(6)-methyl-dG adducts in human lymphoblastoid cells exposed to low dose [D3]-methylnitrosourea. Endogenous amounts of both adducts remained nearly constant, while the exogenous adducts showed linear dose-responses. The data show that O(6)-methyl-dG adducts ≥1.8/10(8) dG correlated with published studies that demonstrated significant increases of mutations under these conditions. The combined results do not support linear extrapolations to zero when data are available for science-based regulations.

摘要

对于具有DNA反应性的化学物质,癌症风险的低剂量线性评估是科学政策的默认方法。在本研究中,我们对暴露于低剂量[D3]-甲基亚硝基脲的人淋巴母细胞中的内源性和外源性N7-甲基-G和O(6)-甲基-dG加合物进行了定量。两种加合物的内源性含量几乎保持不变,而外源性加合物呈现线性剂量反应。数据表明,O(6)-甲基-dG加合物≥1.8/10(8) dG与已发表的研究相关,这些研究表明在这些条件下突变显著增加。当有基于科学的法规可用数据时,综合结果不支持线性外推至零。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d4f/3998766/b9dbfcc8177d/tx-2014-000602_0002.jpg

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