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甲醛潜在共诱变作用的研究。

Investigations on potential co-mutagenic effects of formaldehyde.

机构信息

Universität Ulm, Institut für Humangenetik, 89069 Ulm, Germany.

Universität Ulm, Institut für Humangenetik, 89069 Ulm, Germany.

出版信息

Mutat Res. 2014 Feb;760:48-56. doi: 10.1016/j.mrfmmm.2013.11.007. Epub 2013 Dec 17.

Abstract

The genotoxicity and mutagenicity of formaldehyde (FA) has been well-characterized during the last years. Besides its known direct DNA-damaging and mutagenic activity in sufficiently exposed cells, FA at low concentrations might also enhance the mutagenic and carcinogenic effects of other environmental mutagens by interfering with the repair of DNA lesions induced by these mutagens. To further assess potential co-mutagenic effects of FA, we exposed A549 human lung cells to FA in combination with various mutagens and measured the induction and removal of DNA damage by the comet assay and the production of chromosomal mutations by the cytokinesis-block micronucleus assay (CBMN assay). The mutagens tested were ionizing radiation (IR), (±)-anti-B[a]P-7,8-dihydrodiol-9,10-epoxide (BPDE), N-nitroso-N-methylurea (methyl nitrosourea; MNU) and methyl methanesulfonate (MMS). FA (10-75μM) did not enhance the genotoxic and mutagenic activity of these mutagens under the test conditions applied. FA alone and in combination with MNU or MMS did not affect the expression (mRNA level) of the gene of the O(6)-methylguanine-DNA methyltransferase (MGMT) in A549 cells. The results of these experiments do not support the assumption that low FA concentrations might interfere with the repair of DNA damage induced by other mutagens.

摘要

在过去的几年中,甲醛(FA)的遗传毒性和致突变性得到了很好的描述。除了在充分暴露的细胞中已知的直接 DNA 损伤和致突变活性外,FA 在低浓度下还可能通过干扰这些诱变剂诱导的 DNA 损伤的修复,增强其他环境诱变剂的致突变和致癌作用。为了进一步评估 FA 的潜在协同致突变作用,我们将 A549 人肺细胞暴露于 FA 与各种诱变剂中,并通过彗星试验测量 DNA 损伤的诱导和消除,以及通过胞质分裂阻断微核试验(CBMN 试验)测量染色体突变的产生。测试的诱变剂包括电离辐射(IR)、(±)-反-B[a]P-7,8-二氢二醇-9,10-环氧化物(BPDE)、N-亚硝基-N-甲基脲(甲基亚硝脲;MNU)和甲基甲烷磺酸盐(MMS)。在应用的测试条件下,FA(10-75μM)不会增强这些诱变剂的遗传毒性和致突变活性。FA 单独以及与 MNU 或 MMS 联合使用均不会影响 A549 细胞中 O(6)-甲基鸟嘌呤-DNA 甲基转移酶(MGMT)基因的表达(mRNA 水平)。这些实验的结果不支持低浓度 FA 可能干扰其他诱变剂诱导的 DNA 损伤修复的假设。

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