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用遗传毒性致癌剂 N-乙基-N-亚硝脲处理的小鼠肝脏中 microRNA 时间过程表达的基因组分析。

Genomic analysis of microRNA time-course expression in liver of mice treated with genotoxic carcinogen N-ethyl-N-nitrosourea.

机构信息

Division of Genetic and Molecular Toxicology, National Center for Toxicological Research, FDA, Jefferson, AR 72079, USA.

出版信息

BMC Genomics. 2010 Oct 28;11:609. doi: 10.1186/1471-2164-11-609.

Abstract

BACKGROUND

Dysregulated expression of microRNAs (miRNAs) has been previously observed in human cancer tissues and shown promise in defining tumor status. However, there is little information as to if or when expression changes of miRNAs occur in normal tissues after carcinogen exposure.

RESULTS

To explore the possible time-course changes of miRNA expression induced by a carcinogen, we treated mice with one dose of 120 mg/kg N-ethyl-N-nitrosourea (ENU), a model genotoxic carcinogen, and vehicle control. The miRNA expression profiles were assessed in the mouse livers in a time-course design. miRNAs were isolated from the livers at days 1, 3, 7, 15, 30 and 120 after the treatment and their expression was determined using a miRNA PCR Array. Principal component analysis of the miRNA expression profiles showed that miRNA expression at post-treatment days (PTDs) 7 and 15 were different from those at the other time points and the control. The number of differentially expressed miRNAs (DEMs) changed over time (3, 5, 14, 32, 5 and 5 at PTDs 1, 3, 7, 15, 30 and 120, respectively). The magnitude of the expression change varied with time with the highest changes at PTDs 7 or 15 for most of the DEMs. In silico functional analysis of the DEMs at PTDs 7 and 15 indicated that the major functions of these ENU-induced DEMs were associated with DNA damage, DNA repair, apoptosis and other processes related to carcinogenesis.

CONCLUSION

Our results showed that many miRNAs changed their expression to respond the exposure of the genotoxic carcinogen ENU and the number and magnitude of the changes were highest at PTDs 7 to 15. Thus, one to two weeks after the exposure is the best time for miRNA expression sampling.

摘要

背景

miRNAs 的表达失调已在人类癌症组织中被观察到,并在确定肿瘤状态方面显示出前景。然而,关于致癌剂暴露后正常组织中 miRNA 表达的变化是否发生以及何时发生,知之甚少。

结果

为了探索致癌剂诱导的 miRNA 表达的可能时程变化,我们用 120mg/kg N-乙基-N-亚硝脲(ENU),一种模型遗传毒性致癌剂,对小鼠进行了一次处理,并以载体对照。在时间过程设计中评估了小鼠肝脏中的 miRNA 表达谱。在治疗后第 1、3、7、15、30 和 120 天从肝脏中分离出 miRNA,并使用 miRNA PCR 阵列测定其表达。miRNA 表达谱的主成分分析表明,治疗后第 7 和 15 天的 miRNA 表达与其他时间点和对照不同。差异表达 miRNA(DEM)的数量随时间变化(治疗后第 1、3、7、15、30 和 120 天分别为 3、5、14、32、5 和 5 个)。表达变化的幅度随时间变化而变化,大多数 DEM 的最大变化发生在 PTDs 7 或 15。治疗后第 7 和 15 天的 DEM 的计算机模拟功能分析表明,这些 ENU 诱导的 DEM 的主要功能与 DNA 损伤、DNA 修复、细胞凋亡和其他与致癌作用相关的过程有关。

结论

我们的结果表明,许多 miRNA 改变其表达以响应遗传毒性致癌剂 ENU 的暴露,并且在 PTDs 7 到 15 之间变化的数量和幅度最大。因此,暴露后一到两周是 miRNA 表达采样的最佳时间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f41/3091750/ca091136576b/1471-2164-11-609-1.jpg

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