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体外和体内暴露于呋喃诱导的氧化应激、突变和染色体畸变。

Oxidative Stress, Mutations and Chromosomal Aberrations Induced by In Vitro and In Vivo Exposure to Furan.

机构信息

National Centre for Chemical Products, Cosmetics and Consumer Protection, Istituto Superiore di Sanità, Viale Regina Elena 299, 00161 Rome, Italy.

Oncology and Molecular Medicine, Istituto Superiore di Sanità, Viale Regina Elena 299, 00161 Rome, Italy.

出版信息

Int J Mol Sci. 2021 Sep 7;22(18):9687. doi: 10.3390/ijms22189687.

Abstract

Furan is a volatile compound that is formed in foods during thermal processing. It is classified as a possible human carcinogen by international authorities based on sufficient evidence of carcinogenicity from studies in experimental animals. Although a vast number of studies both in vitro and in vivo have been performed to investigate furan genotoxicity, the results are inconsistent, and its carcinogenic mode of action remains to be clarified. Here, we address the mutagenic and clastogenic activity of furan and its prime reactive metabolite cis-2 butene-1,4-dial (BDA) in mammalian cells in culture and in mouse animal models in a search for DNA lesions responsible of these effects. To this aim, Fanconi anemia-derived human cell lines defective in the repair of DNA inter-strand crosslinks (ICLs) and mice defective in the removal of 8-hydroxyguanine from DNA, were used. We show that both furan and BDA present a weak (if any) mutagenic activity but are clear inducers of clastogenic damage. ICLs are strongly indicated as key lesions for chromosomal damage whereas oxidized base lesions are unlikely to play a critical role.

摘要

呋喃是一种挥发性化合物,在食品的热加工过程中形成。国际权威机构将其归类为可能的人类致癌物,这是基于实验动物致癌性研究的充分证据。尽管已经进行了大量的体外和体内研究来调查呋喃的遗传毒性,但结果不一致,其致癌作用模式仍有待阐明。在这里,我们研究了呋喃及其主要活性代谢物顺-2-丁烯-1,4-二醛(BDA)在培养的哺乳动物细胞和小鼠动物模型中的致突变和断裂活性,以寻找导致这些效应的 DNA 损伤。为此,我们使用了 DNA 链间交联(ICLs)修复缺陷的范可尼贫血症衍生的人类细胞系和 DNA 中 8-羟基鸟嘌呤去除缺陷的小鼠。我们表明,呋喃和 BDA 均具有较弱的(如果有的话)致突变活性,但可明显诱导断裂损伤。ICLs 强烈表明是染色体损伤的关键损伤,而氧化碱基损伤不太可能发挥关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d17e/8465244/74f4cc97b173/ijms-22-09687-g001.jpg

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