Identification, prioritization, and evaluation of glycoproteins for aggressive prostate cancer using quantitative glycoproteomics and antibody-based assays on tissue specimens

被引:53
作者
Chen, Jing [1 ]
Xi, Jiefeng [2 ]
Tian, Yuan [1 ]
Bova, George Steven [3 ]
Zhang, Hui [1 ]
机构
[1] Johns Hopkins Univ, Dept Pathol, Baltimore, MD 21231 USA
[2] Johns Hopkins Univ, Dept Biomed Engn, Baltimore, MD 21231 USA
[3] Univ Tampere, MBPCG, Inst Biosci & Med Technol, FIN-33101 Tampere, Finland
基金
美国国家卫生研究院;
关键词
Aggressive; Biomarker; Glycoproteomics; OC; Prostate cancer; VASCULAR ADHESION PROTEIN-1; BIOMARKER DISCOVERY; STATISTICAL-MODEL; PERIOSTIN; CARTILAGE; EXPRESSION; CELLS; TGF-BETA-1; ISOFORMS; GROWTH;
D O I
10.1002/pmic.201200541
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Prostate cancer is highly heterogeneous in nature; while the majority of cases are clinically insignificant, some cases are lethal. Currently, there are no reliable screening methods for aggressive prostate cancer. Since most established serum and urine biomarkers are glycoproteins secreted or leaked from the diseased tissue, the current study seeks to identify glycoprotein markers specific to aggressive prostate cancer using tissue specimens. With LC-MS/MS glycoproteomic analysis, we identified 350 glycopeptides with 17 being altered in aggressive prostate cancer. ELISA assays were developed/purchased to evaluate four candidates, that is, cartilage oligomeric matrix protein (COMP), periostin, membrane primary amine oxidase (VAP-1), and cathepsin L, in independent tissue sets. In agreement with the proteomic analysis, we found that COMP and periostin expressions were significantly increased in aggressive prostate tumors while VAP-1 expression was significantly decreased in aggressive tumor. In addition, the expression of these proteins in prostate metastases also follows the same pattern observed in the proteomic analysis. COMP and periostin and decrease in VAP-1 expression in the prostate may be associated with aggressive prostate cancer.
引用
收藏
页码:2268 / 2277
页数:10
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