Changes of ECM and CAM gene expression profile in the cirrhotic liver after HCV infection: Analysis by cDNA expression array

被引:6
作者
Xu, Xin [1 ]
Li, Yi-Ming [1 ]
Ji, Hong [1 ]
Hou, Chong-Zhi [1 ]
Cheng, Ying-Bo [1 ]
Ma, Fu-Ping [2 ]
机构
[1] Xi An Jiao Tong Univ, Hosp 2, Dept Gen Surg, Xian 710004, Shaanxi Provinc, Peoples R China
[2] Second Hosp Xianyang, Dept Gen Surg, Xianyang 721000, Shaanxi Provinc, Peoples R China
关键词
Hepatitis C virus; Liver cirrhosis; Extracellular matrix; Cellular adhesion molecules; mRNA array analysis;
D O I
10.3748/wjg.v11.i14.2184
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: We aimed to observe the expression of extracellular matrix (ECM) and cellular adhesion molecules (CAM) in cirrhotic liver tissues after hepatitis C virus (HCV) infection. METHODS: Twelve patients with post HCV inflammatory liver cirrhosis were selected to evaluate their liver function and other virological, pathological parameters. Then three specimens of cirrhotic patients whose health assessment results and laboratory data were similar and three normal liver specimens explanted from liver grafts prepared for liver transplantation were chosen for investigating gene expression of ECM and CAM using cDNA expression array. RESULTS: The cDNA array assay revealed 36.7% (36/96) of genes with changes, in which 26.3% (26/96) was up-regulated and 10.1% (10/96) was down-regulated. Integrin (ITGA), collagen (COL), ADAMTS were identified as the characteristic changes of ECM and CAM gene expression levels. ITGA were demonstrated beta 1 and beta 2 sub-section changed in liver cirrhosis. CONCLUSION: ECM and CAM play an important role in the progression of liver cirrhosis after HCV infection. The capital mechanism is related to the inflammatory cells infiltration, the activation and transformation of ECM producing cells and the imbalance between production and elimination of ECM. (C) 2005 The WJG Press and Elsevier Inc. All rights reserved.
引用
收藏
页码:2184 / 2187
页数:4
相关论文
共 12 条
[1]  
Bedossa Pierre, 2003, Clin Liver Dis, V7, P195, DOI 10.1016/S1089-3261(02)00076-4
[2]   Parenchymal transforming growth factor beta-1: Its type II receptor and Smad signaling pathway correlate with inflammation and fibrosis in chronic liver disease of viral etiology [J].
Calabrese, F ;
Valente, M ;
Giacometti, C ;
Pettenazzo, E ;
Benvegnu, L ;
Alberti, A ;
Gatta, A ;
Pontisso, P .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2003, 18 (11) :1302-1308
[3]  
Kozlowska J, 2001, Przegl Epidemiol, V55, P451
[4]   PAI-1 deficiency attenuates the fibrogenic response to ureteral obstruction [J].
Oda, T ;
Jung, YO ;
Kim, HS ;
Cai, XH ;
López-Guisa, JM ;
Ikeda, Y ;
Eddy, AA .
KIDNEY INTERNATIONAL, 2001, 60 (02) :587-596
[5]  
Olga O. Znoiko, 2003, Current Pharmaceutical Biotechnology, V4, P195, DOI 10.2174/1389201033489810
[6]   Host genetic factors influence disease progression in chronic hepatitis C [J].
Powell, EE ;
Edwards-Smith, CJ ;
Hay, JL ;
Clouston, AD ;
Crawford, DH ;
Shorthouse, C ;
Purdie, DM ;
Jonsson, JR .
HEPATOLOGY, 2000, 31 (04) :828-833
[7]  
Quondamatteo F, 2004, HISTOL HISTOPATHOL, V19, P799, DOI 10.14670/HH-19.799
[8]   The extracellular matrix can regulate vascular cell migration, proliferation, and survival: relationships to vascular disease [J].
Raines, EW .
INTERNATIONAL JOURNAL OF EXPERIMENTAL PATHOLOGY, 2000, 81 (03) :173-182
[9]   Impact of oestrogens on the progression of liver disease [J].
Shimizu, I .
LIVER INTERNATIONAL, 2003, 23 (01) :63-69
[10]  
Shimizu Ichiro, 2001, Current Drug Targets - Infectious Disorders, V1, P227, DOI 10.2174/1568005014606053