Literature DB >> 30802535

Thrombospondin-4 expression as a prognostic marker in hepatocellular carcinoma.

Hongfen Wu1, Guangcong Zhang1, Zhi Li2, Jiamei Ma1, Xiangyang Han3, Tian Xiang4, Xuemei Jiang5.   

Abstract

BACKGROUND AND AIMS: The extracellular calcium-binding protein family member thrombospondin-4 (THBS4) regulates cell migration, proliferation, attachment, adhesion, angiogenesis, neural development, tissue structure, organ development, pain signal transduction, and tumor growth. The aim of this study was to study THBS4 expression in hepatocellular carcinoma (HCC) and determine if it was a prognostic marker for this malignancy.
METHODS: We used immunohistochemistry and tissue microarrays to evaluate THBS4 expression in 84 HCC and matched para-cancerous tissues. Then, we assessed relationships between THBS4 expression and clinicopathological parameters.
RESULTS: THBS4 expression was higher in HCCs than in matched para-cancerous tissues (P < 0.001). There was a significant correlation between high THBS4 levels and preoperative serum alanine aminotransferase (P < 0.04). In HCC patients, high THBS4 expression was associated with shorter overall and disease-free survival compared with low THBS4 expression. Additionally, subgroup analysis showed that high THBS4 levels were only associated with poor overall survival for alpha-fetoprotein >40 ng/mL (P = 0.028) and cirrhosis (P = 0.002). Multivariate analysis showed that high THBS4 expression was an independent prognostic factor for both overall and disease-free survival.
CONCLUSIONS: Our data suggest that THBS4 may play a role in HCC development, and thus may be an independent prognostic marker and/or potential therapeutic target for HCC patients.
Copyright © 2019 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Clinicopathological feature; Hepatocellular carcinoma; Prognostic marker; Thrombospondin-4; Tissue microarray

Mesh:

Substances:

Year:  2019        PMID: 30802535     DOI: 10.1016/j.gene.2019.02.049

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


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