Alterations in expressed prostate secretion-urine PSA N-glycosylation discriminate prostate cancer from benign prostate hyperplasia

  • Oncotarget. 2017 Aug 16;8(44):76987-76999. doi: 10.18632/oncotarget.20299.
Gaozhen Jia  #  1 Zhenyang Dong  #  1 Chenxia Sun  2 Fuping Wen  2 Haifeng Wang  1 Huaizu Guo  3 Xu Gao  1 Chuanliang Xu  1 Chuanliang Xu  1 Chenghua Yang  4  2 Yinghao Sun  1
Affiliations
  • 1. Department of Urology, Changhai Hospital, Second Military Medical University, Shanghai 2000433, China.
  • 2. Institute for Nutritional Sciences, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, China.
  • 3. State Key Laboratory of Antibody Medicine and Targeted Therapy, Shanghai 201203, China.
  • 4. Joint Center for Translational Research of Chronic Diseases, Changhai Hospital, Second Military Medical University, Shanghai 2000433, China.
  • # Contributed equally.
Abstract

The prostate specific antigen (PSA) test is widely used for early diagnosis of prostate Cancer (PCa). However, its limited sensitivity has led to over-diagnosis and over-treatment of PCa. Glycosylation alteration is a common phenomenon in Cancer development. Different PSA glycan subforms have been proposed as diagnostic markers to better differentiate PCa from benign prostate hyperplasia (BPH). In this study, we purified PSA from expressed prostate secretions (EPS)-urine samples from 32 BPH and 30 PCa patients and provided detailed PSA glycan profiles in Chinese population. We found that most of the PSA glycans from EPS-urine were complex type biantennary glycans. We observed two major patterns in PSA glycan profiles. Overall there was no distinct separation of PSA glycan profiles between BPH and PCa patients. However, we detected a significant increase of glycan FA2 and FM5A2G2S1 in PCa when compared with BPH patients. Furthermore, we observed that the composition of FA2 glycan increased significantly in advanced PCa with Gleason score ≥8, which potentially could be translated to clinic as a marker for aggressive PCa.

Keywords
EPS-urine; PSA; benign prostate hyperplasia; glycosylation; prostate cancer.
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