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Hepatic Temporal Gene Expression Profiling in Helicobacter hepaticus-Infected A/JCr Mice.

机译:肝感染Helicobacter A / JCr小鼠的肝时态基因表达谱。

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摘要

Helicobacter hepaticusinfection of A/JCr mice is a model of infectious liver cancer. We monitored hepatic global gene expression profiles inH. hepaticusinfected and control male A/JCr mice at 3 months, 6 months, and 1 year of age using an Affymetrix-based oligonucleotide microarray platform on the premise that a specific genetic expression signature at isolated time points would be indicative of disease status. Model based expression index comparisons generated by dChip yielded consistent profiles of differential gene expression forH. hepaticusinfected male mice with progressive liver disease versus uninfected control mice within each age group. Linear discriminant analysis and principal component analysis allowed segregation of mice based on combined age and lesion status, or age alone. Up-regulation of putative tumor markers correlated with advancing hepatocellular dysplasia. Transcriptionally down-regulated genes in mice with liver lesions included those related to peroxisome proliferator, fatty acid, and steroid metabolism pathways. In conclusion, transcriptional profiling of hepatic genes documented gene expression signatures in the livers ofH. hepaticusinfected male A/JCr mice with chronic progressive hepatitis and preneoplastic liver lesions, complemented the histopathological diagnosis, and suggested molecular targets for the monitoring and intervention of disease progression prior to the onset of hepatocellular neoplasia.
机译:A / JCr小鼠的肝杆菌感染是传染性肝癌的模型。我们监测了H中的肝全局基因表达谱。使用基于Affymetrix的寡核苷酸微阵列平台,在3个月,6个月和1岁时,感染肝和雄性A / JCr的雄性A / JCr小鼠为前提,前提是在孤立的时间点有特定的基因表达特征可以指示疾病状态。 dChip生成的基于模型的表达指数比较产生了H差异基因表达的一致图谱。在每个年龄组中,肝炎感染的具有进展性肝病的雄性小鼠与未感染的对照小鼠相比。线性判别分析和主成分分析允许根据合并的年龄和病变状态或单独的年龄对小鼠进行隔离。推定的肿瘤标志物的上调与进展性肝细胞异型增生相关。肝损伤小鼠的转录下调基因包括与过氧化物酶体增殖物,脂肪酸和类固醇代谢途径有关的基因。总之,肝基因的转录谱记录了H肝中的基因表达特征。肝感染的雄性A / JCr小鼠患有慢性进行性肝炎和前肿瘤形成性肝损害,补充了组织病理学诊断,并提出了在肝细胞瘤形成之前监测和干预疾病进展的分子靶点。

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