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2017 ; 7
(ä): 43446
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Characterization of gene expression profiles in HBV-related liver fibrosis
patients and identification of ITGBL1 as a key regulator of fibrogenesis
#MMPMID28262670
Wang M
; Gong Q
; Zhang J
; Chen L
; Zhang Z
; Lu L
; Yu D
; Han Y
; Zhang D
; Chen P
; Zhang X
; Yuan Z
; Huang J
; Zhang X
Sci Rep
2017[Mar]; 7
(ä): 43446
PMID28262670
show ga
Although hepatitis B virus (HBV) infection is the leading cause of liver fibrosis
(LF), the mechanisms underlying liver fibrotic progression remain unclear. Here,
we investigated the gene expression profiles of HBV-related LF patients. Whole
genome expression arrays were used to detect gene expression in liver biopsy
samples from chronically HBV infected patients. Through integrative data
analysis, we identified several pathways and key genes involved in the initiation
and exacerbation of liver fibrosis. Weight gene co-expression analysis revealed
that integrin subunit ?-like 1 (ITGBL1) was a key regulator of fibrogenesis.
Functional experiments demonstrated that ITGBL1 was an upstream regulator of LF
via interactions with transforming growth factor ?1. In summary, we investigated
the gene expression profiles of HBV-related LF patients and identified a key
regulator ITGBL1. Our findings provide a foundation for future studies of gene
functions and promote the development of novel antifibrotic therapies.
|*Gene Expression Regulation
[MESH]
|*Host-Pathogen Interactions
[MESH]
|Biomarkers/metabolism
[MESH]
|Gene Expression Profiling
[MESH]
|Gene Ontology
[MESH]
|Hepatitis B Antibodies/genetics/metabolism
[MESH]
|Hepatitis B Surface Antigens/genetics/metabolism
[MESH]
|Hepatitis B e Antigens/genetics/metabolism
[MESH]
|Hepatitis B virus/pathogenicity/physiology
[MESH]