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Authors Luo D, Chen W, Tian Y, Li J, Xu X, Chen C, Li F
Received 23 January 2017
Accepted for publication 23 March 2017
Published 18 April 2017 Volume 2017:10 Pages 2173—2181
DOI https://doi.org/10.2147/OTT.S133022
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Akshita Wason
Peer reviewer comments 2
Editor who approved publication: Dr Ingrid Espinoza
Abstract: Glioma is the most common and aggressive human primary tumor in the
central nervous system. Despite present clinical advancements, median survival
time remains poor in this malignant tumor. Serpin peptidase inhibitor, clade A
member 3 (SERPINA3), is a member of the serpin superfamily of protease
inhibitors. Its aberrant expression has been observed in various tumors.
However, its clinical significance and biological function in glioma remain
unclear, especially for the prognosis of glioma patients. In this study, we
investigated SERPINA3 expression in glioma tissue samples and its significance
in predicting the prognosis of glioma patients. SERPINA3 protein expression was
studied by immunohistochemistry, while real-time polymerase chain reaction was
used to study SERPINA3 mRNA expression. We found that SERPINA3 was upregulated
in glioma tissue at both mRNA and protein levels, compared with noncancerous
brain tissues. We also found that high SERPINA3 expression in glioma tissues
correlated significantly with advanced World Health Organization grade.
Univariate and multivariate analyses revealed that high SERPINA3 expression was
an independent prognostic factor for poor overall survival of glioma patients.
Moreover, our findings were further validated by online Oncomine database.
Taken together, our results suggest that SERPINA3 plays an oncogenic role in
glioma progression and provide an insight into the application of SERPINA3 as a
novel predictor of clinical outcomes and a potential biomarker of glioma.
Keywords: SERPINA3, immunohistochemistry,
glioblastoma, prognosis, glioma