Oncotarget

Research Papers:

Co-expression of Piwil2/Piwil4 in nucleus indicates poor prognosis of hepatocellular carcinoma

Guangping Zeng, Deying Zhang, Xing Liu, Qing Kang, Yiyao Fu, Bo Tang, Wenhao Guo, Yuanyuan Zhang, Guanghui Wei and Dawei He _

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Oncotarget. 2017; 8:4607-4617. https://doi.org/10.18632/oncotarget.13491

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Abstract

Guangping Zeng1,*, Deying Zhang1,*, Xing Liu1, Qing Kang1, Yiyao Fu1, Bo Tang1, Wenhao Guo1, Yuanyuan Zhang2, Guanghui Wei1, Dawei He1

1Department of Urology, Children’s Hospital of Chongqing Medical University, Ministry of Education Key Laboratory of Child Development and Disorders, Key Laboratory of Pediatrics in Chongqing, Chongqing International Science and Technology Cooperation Center for Child Development and Disorders, Chongqing 400014, China

2Wake Forest Institute for Regenerative Medicine, Wake Forest University School of Medicine, Medical Center Blvd, Winston-Salem, North Carolina 27103, USA

*These authors have contributed equally to this work

Correspondence to:

Dawei He, email: dw.he@163.com

Keywords: hepatocellular carcinoma, molecular chaperone, Piwil2, Piwil4, prognosis

Received: July 25, 2016     Accepted: October 28, 2016     Published: November 22, 2016

ABSTRACT

Purpose: This study aimed to explore the localization and expression of P-element-induced wimpy testis-like 2 (piwil2)/Piwil4 in hepatocellular carcinoma (HCC) tissues, and analyze the correlation between co-expression pattern and prognosis of HCC.

Results: Piwil2 showed 100% positive expression in the cell nucleus, with the intensity higher than in the cytoplasm. Piwil4 showed a lower intensity of expression in the cell nucleus than in the cytoplasm. The molecular chaperone Piwil2/Piwil4 had four co-expression patterns: nuclear co-expression, nuclear and cytoplasmic co-expression, cytoplasmic co-expression, and non-coexpression. The survival rate and the overall survival sequentially increased. The prognostic phenotype of the nuclear co-expression of Piwil2/Piwil4 was worse than that of non-coexpression, and the intracellular localization and expression of Piwil2 and Piwil4 were not significantly different.

Methods: HCC pathological tissue samples with follow-up information (90 cases) and 2 normal control liver tissues were collected and made into a 92-site microarray. The expression of Piwil2 and Piwil4 was detected using the immunofluorescence double staining method. The differences in the expression and location of Piwil2 and Piwil4 in tumor cells were explored, and the influence of such differences on the long-term survival rate of HCC was studied using Kaplan-Meier survival curve and log-rank test. The clinical staging was analyzed according to the HCC international TNM staging criteria.

Conclusions: The nuclear co-expression of Piwil2/Piwil4 indicated that patients with HCC had a worse prognostic phenotype. The molecular chaperone Piwil2/Piwil4 seems promising as a molecular marker for prognosis judgment; a single marker (Piwil2/Piwil4) cannot be used for prognosis judgment.


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