2015
DOI: 10.1111/liv.12877
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Increased Pygo2 expression in liver of patients with hepatitis B virus‐related fibrosis

Abstract: This study suggested that Pygo2 was involved in HBV-induced liver fibrogenesis. Pygo2 is a valuable biomarker for the evaluation of fibrosis in HBV-infected patients.

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Cited by 4 publications
(3 citation statements)
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“…Other studies linking HBV to Wnt report upregulated DVL3 , upregulation of Wnt1 protein on HBV infected HCC patients (20) and upregulation of Wnt3a and FZD7 in HBV associated HCC samples (21). An association between AXIN1 variants and HBV‐associated HCC has also been found , plus an association between HBV‐associated liver fibrosis and the key Wnt mediator, Pygo2 .…”
Section: Viruses Implicated In Human Cancer Developmentmentioning
confidence: 96%
“…Other studies linking HBV to Wnt report upregulated DVL3 , upregulation of Wnt1 protein on HBV infected HCC patients (20) and upregulation of Wnt3a and FZD7 in HBV associated HCC samples (21). An association between AXIN1 variants and HBV‐associated HCC has also been found , plus an association between HBV‐associated liver fibrosis and the key Wnt mediator, Pygo2 .…”
Section: Viruses Implicated In Human Cancer Developmentmentioning
confidence: 96%
“…The dynamic expression of Pygo2 is important for maintaining the development of various organs and manipulates the differentiation of multiple cell types 10,11 . Pygo2 was recently reported to mediate β‐Catenin activity in a gene‐ or tissue‐dependent manner in different physiological processes 12,13 . A meaningful study showed that Pygo2 expression decreased gradually during 3 T3‐L1 preadipocyte differentiation, and pygo2 −/− mice exhibited spontaneous adipogenesis by inhibiting the expression of peroxisome proliferator‐activated receptor γ (PPARγ) 14 .…”
Section: Introductionmentioning
confidence: 99%
“… 10 , 11 Pygo2 was recently reported to mediate β‐Catenin activity in a gene‐ or tissue‐dependent manner in different physiological processes. 12 , 13 A meaningful study showed that Pygo2 expression decreased gradually during 3 T3‐L1 preadipocyte differentiation, and pygo2 −/− mice exhibited spontaneous adipogenesis by inhibiting the expression of peroxisome proliferator‐activated receptor γ (PPARγ). 14 However, the expression and contribution of Pygo2 in the pathogenesis of CD has not been elucidated.…”
Section: Introductionmentioning
confidence: 99%