Hepatic temporal gene expression profiling in Helicobacter hepaticus-infected A/JCr mice

被引:23
作者
Boutin, SR
Rogers, AB
Shen, Z
Fry, RC
Love, JA
Nambiar, PR
Suerbaum, S
Fox, JG
机构
[1] MIT, Div Comparat Med, Cambridge, MA 02139 USA
[2] MIT, Div Biol Engn, Cambridge, MA 02139 USA
[3] MIT, Computat & Syst Biol Initiat, Cambridge, MA 02139 USA
[4] MIT, Whitehead Inst Biomed Res, Cambridge, MA 02139 USA
[5] Hannover Med Sch, Inst Med Microbiol & Hosp Epidemiol, D-3000 Hannover, Germany
关键词
microarray; hepatitis; chronic; carcinoma; hepatocellular; mice; inbred; Helicobacter;
D O I
10.1080/01926230490524058
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Helicobacter hepaticus infection of A/JCr mice is a model of infectious liver cancer. We monitored hepatic global gene expression profiles in H. hepaticus infected 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 for H. hepaticus infected 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 of H. hepaticus infected 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.
引用
收藏
页码:678 / 693
页数:16
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