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首页> 外文期刊>Toxicology: An International Journal Concerned with the Effects of Chemicals on Living Systems >Effects of long-term low-dose cadmium exposure on genomic DNA methylation in human embryo lung fibroblast cells.
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Effects of long-term low-dose cadmium exposure on genomic DNA methylation in human embryo lung fibroblast cells.

机译:长期低剂量镉暴露对人胚肺成纤维细胞基因组DNA甲基化的影响。

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摘要

Cadmium is a toxic transition metal of continuing occupational and environmental concern. As a well-recognized human carcinogen, its carcinogenic mechanisms are still poorly understood. Cadmium has long been considered a non-genotoxic carcinogen and thought to act through epigenetic mechanisms. In the present study, we tested the effects of long-term low-dose cadmium exposure on DNA methylation in human embryo lung fibroblast (HLF) cells. After 2 months of exposure to 0-1.5mumol/L cadmium, both the level of genomic DNA methylation and the enzyme activity of DNA methyltransferases (DNMTs) were increased in a concentration-related manner. Moreover, our results showed that cadmium exposure up-regulated the mRNA levels of DNMT1, DNMT3a and DNMT3b at higher concentrations. We further tested the growth dynamics of HLF cells, and observed significantly elevated growth rates, decreased cell population of G0/G1-phase and increased cell population of S-phase at 0.9, 1.2, and 1.5mumol/L concentrations. Our study indicated that long-term low-dose cadmium exposure could disrupt DNA methylation, which may be one of the possible underlying carcinogenic mechanisms of cadmium.
机译:镉是一种持续引起职业和环境关注的有毒过渡金属。作为一种公认的人类致癌物,其致癌机理仍知之甚少。长期以来,镉一直被认为是非遗传毒性致癌物,并被认为通过表观遗传机制起作用。在本研究中,我们测试了长期低剂量镉暴露对人胚肺成纤维细胞(HLF)细胞DNA甲基化的影响。暴露于0-1.5μmol/ L的镉2个月后,基因组DNA甲基化水平和DNA甲基转移酶(DNMT)的酶活性均以浓度相关的方式增加。而且,我们的结果表明,镉暴露在较高浓度下上调了DNMT1,DNMT3a和DNMT3b的mRNA水平。我们进一步测试了HLF细胞的生长动力学,并观察到在0.9、1.2和1.5mumol / L的浓度下,生长速率显着提高,G0 / G1期细胞数量减少,S期细胞数量增加。我们的研究表明,长期低剂量摄入镉可能会破坏DNA甲基化,这可能是镉潜在的潜在致癌机制之一。

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