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High SPOCK1 Expression Is Associated with Advanced Stage, T Value, and Gleason Grade in Prostate Cancer

Authors
  • Chen, Mei-Ling1
  • Ho, Cheng-Ju2
  • Yeh, Chung-Min1, 3
  • Chen, Sung-Lang2, 4, 5
  • Sung, Wen-Wei2, 4, 5
  • Wang, Shao-Chuan2, 4, 5
  • Chen, Chih-Jung1, 3, 4
  • 1 Department of Surgical Pathology, Changhua Christian Hospital, Changhua 50006, Taiwan
  • 2 Department of Urology, Chung Shan Medical University Hospital, Taichung 40201, Taiwan
  • 3 Department of Medical Technology, Jen-Teh Junior College of Medicine, Nursing and Management, Miaoli 35664, Taiwan
  • 4 School of Medicine, Chung Shan Medical University, Taichung 40201, Taiwan
  • 5 Institute of Medicine, Chung Shan Medical University, Taichung 40201, Taiwan
Type
Published Article
Journal
Medicina
Publisher
MDPI
Publication Date
Jul 05, 2019
Volume
55
Issue
7
Identifiers
DOI: 10.3390/medicina55070343
PMID: 31284511
PMCID: PMC6681093
Source
PubMed Central
Keywords
License
Green

Abstract

Background and objectives : Prostate cancer (PCa) is a common malignancy in males and has a relatively slower progression than other cancers. Our goal was to evaluate the clinical role of SPARC (secreted protein acidic and cysteine rich, osteonectin), cwcv, and kazal-like domains’ proteoglycan 1 (SPOCK1) in PCa. Materials and Methods : SPOCK1 expression was studied through the immunohistochemical staining of specimens from 71 patients with PCa. The correlation between SPOCK1 expression and clinicopathological features was quantitatively analyzed. We used Kaplan–Meier analysis and Cox proportional hazard models to analyze the prognostic value. Results : Of 71 PCa patients, high SPOCK1 expression was more likely to be seen in those with an advanced stage ( p = 0.018) of the disease and an advanced tumor (T) value ( p = 0.014). Patients in Gleason grade groups 3 and 4 had significantly higher SPOCK1 expression ( p = 0.044 and 0.003, respectively) compared to those of Gleason grade group 1. However, this trend was not observed in patients in Gleason grade group 5. For the survival analysis, although it was not statistically significant, patients with a high SPOCK1 expression had a shorter median overall survival (6.2 years) compared to those with low expression (7.8 years). Conclusions : High SPOCK1 expression may be related to advanced clinicopathological features and possibly a poor prognosis. Further analysis with a larger patient base would help clarify this issue.

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