首页> 外文期刊>Food and Chemical Toxicology: An International Journal Published for the British Industrial Biological Research >Effects of sulfur dioxide derivatives on expression of oncogenes and tumor suppressor genes in human bronchial epithelial cells.
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Effects of sulfur dioxide derivatives on expression of oncogenes and tumor suppressor genes in human bronchial epithelial cells.

机译:二氧化硫衍生物对人支气管上皮细胞癌基因和抑癌基因表达的影响。

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摘要

Sulfur dioxide (SO(2)) is a major air pollutant suspected to act as a promoter or co-carcinogen. The present study was designed to investigate whether SO(2) derivatives (bisulfite and sulfite) had effects on the expression of several proto-oncogenes and tumor suppressor genes in cultured human bronchial epithelial (BEP2D) cells. The mRNA and protein levels were measured by real-time RT-PCR and western blotting, respectively, following exposure to differing SO(2)-derivative concentrations and exposure times. SO(2) derivatives caused mRNA and protein over-expression of c-fos, c-jun, and c-myc at all tested doses (0.001-2mM). Over-expression of H-ras and p53 were observed in cells receiving the highest concentration (0.1-2mM), as well as the under-expression of p16 and Rb. The over-expression of c-fos and c-jun was observed after 24h recovery. The expression of c-myc and H-ras decreased to base line levels while the p53 expression decreased compared with control after 24h recovery. The mRNA and protein expression of p16 and Rb remained at initial levels after 24h recovery. The data support the hypothesis that SO(2) derivatives could cause the activation of proto-oncogenes and inactivation of tumor suppressor genes and SO(2) derivatives may play a role in the pathogenesis of SO(2)-associated lung cancer.
机译:二氧化硫(SO(2))是一种主要的空气污染物,被怀疑是起促进剂或助癌作用。本研究旨在调查SO(2)衍生物(亚硫酸氢盐和亚硫酸盐)是否对培养的人支气管上皮细胞(BEP2D)中几种原癌基因和抑癌基因的表达产生影响。分别暴露于不同的SO(2)衍生物浓度和暴露时间后,分别通过实时RT-PCR和Western blotting测量mRNA和蛋白水平。 SO(2)衍生物导致在所有测试剂量(0.001-2mM)下c-fos,c-jun和c-myc的mRNA和蛋白质过度表达。在接受最高浓度(0.1-2mM)的细胞中观察到H-ras和p53的过表达,以及p16和Rb的过表达。恢复24小时后观察到c-fos和c-jun的过度表达。恢复24小时后,与对照组相比,c-myc和H-ras的表达下降至基线水平,而p53表达下降。恢复24小时后,p16和Rb的mRNA和蛋白质表达保持在初始水平。数据支持这一假设,即SO(2)衍生物可能导致原癌基因的激活和抑癌基因的失活,而SO(2)衍生物可能在与SO(2)相关的肺癌的发病机理中起作用。

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