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Published in: Diagnostic Pathology 1/2014

Open Access 01-12-2014 | Research

AKR1C3 overexpression may serve as a promising biomarker for prostate cancer progression

Authors: Yuantong Tian, Lijing Zhao, Haitao Zhang, Xichun Liu, Lijuan Zhao, Xuejian Zhao, Yi Li, Jing Li

Published in: Diagnostic Pathology | Issue 1/2014

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Abstract

Background

Aldo-keto reductase family 1 member C3 (AKR1C3) is a key steroidogenic enzyme that is overexpressed in prostate cancer (PCa) and is associated with the development of castration-resistant prostate cancer (CRPC). The aim of this study was to investigate the correlation between the expression level of AKR1C3 and the progression of PCa.

Methods

Sixty human prostate needle biopsy tissue specimens and ten LNCaP xenografts from intact or castrated male mice were included in the study. The relationship between the level of AKR1C3 expression by immunohistochemistry and evaluation factors for PCa progression, including prostate-specific antigen (PSA), Gleason score (GS) and age, were analyzed.

Results

Low immunoreactivity of AKR1C3 was detected in normal prostate epithelium, benign prostatic hyperplasia (BPH) and prostatic intraepithelial neoplasia (PIN). Positive staining was gradually increased with an elevated GS in PCa epithelium and LNCaP xenografts in mice after castration. The Spearman’s r values (rs) of AKR1C3 to GS and PSA levels were 0.396 (P = 0.025) and -0.377 (P = 0.036), respectively, in PCa biopsies. The rs of AKR1C3 to age was 0.76 (P = 0.011). No statistically significant difference was found with other variables.

Conclusion

Our study suggests that the level of AKR.
1C3 expression is positively correlated with an elevated GS, indicating that AKR1C3 can serve as a promising biomarker for the progression of PCa.

Virtual slides

The virtual slide(s) for this article can be found here: http://​www.​diagnosticpathol​ogy.​diagnomx.​eu/​vs/​7748245591110149​.
Appendix
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Metadata
Title
AKR1C3 overexpression may serve as a promising biomarker for prostate cancer progression
Authors
Yuantong Tian
Lijing Zhao
Haitao Zhang
Xichun Liu
Lijuan Zhao
Xuejian Zhao
Yi Li
Jing Li
Publication date
01-12-2014
Publisher
BioMed Central
Published in
Diagnostic Pathology / Issue 1/2014
Electronic ISSN: 1746-1596
DOI
https://doi.org/10.1186/1746-1596-9-42

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