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首页> 外文期刊>Archives of Toxicology >Combined effects of okadaic acid and cadmium on lipid peroxidation and DNA bases modifications (m5dC and 8-(OH)-dG) in Caco-2 cells.
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Combined effects of okadaic acid and cadmium on lipid peroxidation and DNA bases modifications (m5dC and 8-(OH)-dG) in Caco-2 cells.

机译:冈田酸和镉对Caco-2细胞脂质过氧化和DNA碱基修饰(m5dC和8-(OH)-dG)的联合作用。

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Okadaic acid (OA) is a marine toxin, a tumour promoter and an inducer of apoptosis. It mainly inhibits protein-phosphatases, protein synthesis and enhances lipid peroxidation. Cadmium (Cd) is known to be carcinogenic in animals and humans (group 1 according to the International Agency for Research on Cancer (IARC) classification). Cd also induces oxidative stress in living organisms. Since they are sometimes found simultaneously in mussels, we have evaluated in the present investigation, the lipid peroxidation, as malondialdehyde (MDA) production, in the variation of the ratios of 8-(OH)-dG/10(5)dG and m5dC/(dC + m5dC) induced by OA and/or Cd in Caco-2 cells. When cells were treated exclusively by OA (15 ng/ml) or Cd (0.625 and 5 microg/ml) for 24 h, protein synthesis was inhibited (by 42 +/- 5%, 18 +/- 13%, and 90 +/- 4% respectively) while MDA production was 2,235 +/- 129, 1710 +/- 20, and 11,496 +/-1,624 pmol/mg protein respectively. In addition, each toxicant induced modified bases in DNA; increases in oxidised bases and methylated dC. The combination of OA and cadmium was more cytotoxic and caused more DNA base modifications; the ratio m(5)dC/(m(5)dC + dC) was increased from 3 +/- 0.15 to 9 +/- 0.15 and the ratio 8-(OH)-dG/10(5) dG also (from 36 +/- 2 to 76 +/- 6). The combination of OA and Cd also increased the level of MDA (1,6874 +/- 2,189 pmole/mg protein). The present results strongly suggest that DNA damage resulting from the oxidative stress induced by these two toxicants may significantly contribute to increasing their carcinogenicity via epigenetic processes.
机译:冈田酸(OA)是一种海洋毒素,是肿瘤的启动子和细胞凋亡的诱导剂。它主要抑制蛋白质磷酸酶,蛋白质合成并增强脂质过氧化作用。已知镉(Cd)在动物和人类中具有致癌性(根据国际癌症研究机构(IARC)分类为第1组)。镉还诱导生物体内的氧化应激。由于有时在贻贝中同时发现它们,因此在本研究中,我们评估了脂质过氧化作为丙二醛(MDA)产生的8-(OH)-dG / 10(5)dG和m5dC比率的变化OA和/或Cd在Caco-2细胞中诱导的/(dC + m5dC)。当仅用OA(15 ng / ml)或Cd(0.625和5 microg / ml)处理细胞24小时时,蛋白质合成受到抑制(分别为42 +/- 5%,18 +/- 13%和90 + (分别为4%),而MDA的产生量分别为2,235 +/- 129、1710 +/- 20和11,496 +/- 1,624 pmol / mg蛋白质。此外,每种有毒物质都会诱导DNA中的修饰碱基。氧化碱和甲基化dC增加。 OA和镉的组合具有更高的细胞毒性,并引起更多的DNA碱基修饰。比率m(5)dC /(m(5)dC + dC)从3 +/- 0.15增加到9 +/- 0.15,比率8-(OH)-dG / 10(5)dG也从( 36 +/- 2至76 +/- 6)。 OA和Cd的组合也增加了MDA的水平(1,6874 +/- 2,189 pmole / mg蛋白)。目前的结果有力地表明,由这两种有毒物质引起的氧化应激导致的DNA损伤可能通过表观遗传过程大大促进了其致癌性。

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