首页> 外文期刊>Toxicological sciences: An official journal of the Society of Toxicology >DNA hypermethylation of promoter of gene p53 and p16 in arsenic-exposed people with and without malignancy.
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DNA hypermethylation of promoter of gene p53 and p16 in arsenic-exposed people with and without malignancy.

机译:p53和p16基因启动子的DNA超甲基化在有和没有恶性肿瘤的砷接触人群中。

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摘要

Chronic arsenic exposure is known to produce arsenicosis and cancer. To ascertain whether perturbation of methylation plays a role in such carcinogenesis, the degree of methylation of p53 and p16 gene in DNA obtained from blood samples of people chronically exposed to arsenic and skin cancer subjects was studied. Methylation-specific restriction endonuclease digestion followed by polymerase chain reaction (PCR) of gene p53 and bisulfite treatment followed by methylation-sensitive PCR of gene p16 have been carried out to analyze the methylation status of the samples studied. Significant DNA hypermethylation of promoter region of p53 gene was observed in DNA of arsenic-exposed people compared to control subjects. This hypermethylation showed a dose-response relationship. Further, hypermethylation of p53 gene was also observed in arsenic-induced skin cancer patients compared to subjects having skin cancer unrelated to arsenic, though not at significant level. However, a small subgroup of cases showed hypomethylation with high arsenic exposure. Significant hypermethylation of gene p16 was also observed in cases of arsenicosis exposed to high level of arsenic. In man, arsenic has the ability to alter DNA methylation patterns in gene p53 and p16, which are important in carcinogenesis.
机译:已知长期暴露于砷会导致砷中毒和癌症。为了确定甲基化的扰动是否在这种致癌作用中起作用,研究了从长期暴露于砷和皮肤癌患者的人的血液样本中获得的DNA中p53和p16基因的甲基化程度。已经进行了甲基化特异性限制性内切核酸酶消化,基因p53的聚合酶链反应(PCR)和亚硫酸氢盐处理,基因p16的甲基化敏感PCR的分析,以分析所研究样品的甲基化状态。与对照组相比,暴露于砷的人的DNA中观察到了p53基因启动子区域的显着DNA超甲基化。这种高甲基化显示出剂量-反应关系。此外,与具有与砷无关的皮肤癌的受试者相比,在砷诱导的皮肤癌患者中也观察到了p53基因的高甲基化,尽管其水平不是很高。但是,一小部分病例显示甲基化水平低,砷暴露量高。在暴露于高水平砷的砷中毒病例中,还观察到了基因p16的显着高甲基化。在人类中,砷具有改变基因p53和p16中DNA甲基化模式的能力,这在致癌作用中很重要。

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