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Abnormal nuclear expression of Pygopus‐2 in human primary hepatocellular carcinoma correlates with a poor prognosis
Author(s) -
Zhang Sheng,
Li Jie,
He Fei,
Wang XiaoMin
Publication year - 2015
Publication title -
histopathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.626
H-Index - 124
eISSN - 1365-2559
pISSN - 0309-0167
DOI - 10.1111/his.12637
Subject(s) - hepatocellular carcinoma , immunohistochemistry , surgical oncology , wnt signaling pathway , cancer , pathology , metastasis , medicine , oncology , cancer research , biology , signal transduction , biochemistry
Aims Pygopus‐2 (Pygo2) is a critical element of the canonical Wnt/β‐catenin transcriptional complex. The aim of the present study was to investigate the expression patterns and clinicopathological significance of Pygo2 in human primary hepatocellular carcinoma ( HCC ). Methods and results Real‐time polymerase chain reaction ( PCR ) analysis of the m RNA levels of Pygo2 in 50 paired HCC cancer/adjacent non‐cancerous tissues showed that Pygo2 m RNA expression was significantly higher in cancerous tissues ( P  =   0.009). Immunohistochemical analysis showed that abnormal Pygo2 protein expression in HCC patients was associated with age ( P  =   0.025), tumour size ( P  =   0.005), intra‐ or extra‐hepatic metastasis ( P  =   0.029), vascular invasion ( P  =   0.026) and tumour differentiation ( P  =   0.004). Patients with normal Pygo2 protein expression showed a longer survival time ( P  =   0.031) and a higher 1‐year survival rate ( P  =   0.032) than those with abnormal Pygo2 expression. Cox's proportional hazard regression model showed that abnormal Pygo2 protein expression was a risk factor associated with the prognosis of HCC patients ( P  =   0.043). Conclusion To the best of our knowledge, this is the first report investigating Pygo2 expression patterns and their clinicopathological significance in HCC . Our findings suggest that Pygo2 may be an important predictor of poor outcome in HCC patients, and could serve as a novel biomarker for HCC .

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