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Toxicological effects of benzo[a]pyrene on DNA methylation of whole genome in ICR mice

机译:苯并[a] py对ICR小鼠全基因组DNA甲基化的毒理作用

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It has been well known that alterations in DNA methylation - an important regulator of gene transcription - lead to cancer. Therefore a change in the level of DNA methylation of whole genome has been considered as a biomarker of carcinogenesis. Previously, a large number of experimental results in genetic toxicology have showed that benzo[a]pyrene could cause DNA mutation and fragmentation. However, there was little to no studies on alterations in DNA methylation of genome directly result from exposure to benzo[a]pyrene. In this paper, possible mechanisms of alterations in whole genomic DNA methylation by benzo[a]pyrene were investigated using ICR mice after benzo[a]pyrene exposure. The blood, liver, pancreas, skin, lung and bladder of ICR mice were removed and checked after a fixed time interval (6 hours) of benzo[a]pyrene exposure, and whole genomic DNA methylation level was determined by high performance liquid chromatography (HPLC). The results exhibited tissue specificity, that is, the level of whole genomic DNA methylation decreases significantly in blood and liver, rather than pancreas, lung, skin and bladder of ICR mice. This study investigated the direct relationship between aberrant DNA methylation level and benzo[a]pyrene exposure, which might be helpful to clarify the toxicological mechanism of benzo[a] pyrene in epigenetic perspectives.
机译:众所周知,DNA甲基化的改变(一种重要的基因转录调节剂)会导致癌症。因此,整个基因组DNA甲基化水平的变化被认为是致癌的生物标志。以前,遗传毒理学的大量实验结果表明,苯并[a] py可能引起DNA突变和断裂。然而,很少或没有关于暴露于苯并[a] py直接导致的基因组DNA甲基化改变的研究。在本文中,使用ICR小鼠研究了苯并[a] re暴露后苯并[a] whole改变整个基因组DNA甲基化的可能机制。在固定时间间隔(6小时)苯并[a] exposure暴露后,取出并检查ICR小鼠的血液,肝脏,胰腺,皮肤,肺和膀胱,并通过高效液相色谱法测定整个基因组DNA甲基化水平( HPLC)。结果显示出组织特异性,即在ICR小鼠的血液和肝脏中,而不是胰腺,肺,皮肤和膀胱中,全基因组DNA甲基化水平显着降低。这项研究调查了异常DNA甲基化水平与苯并[a] exposure暴露之间的直接关系,这可能有助于从表观遗传学角度阐明苯并[a] ene的毒理机制。

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