PubMed:29502397 / 0-3 JSONTXT

An In-depth Glycosylation Assay for Urinary Prostate Specific Antigen. The concentration of prostate specific antigen (PSA) in serum is used as an early detection method of prostate cancer (PCa) showing, however, low sensitivity, specificity and a poor predictive value. Initial studies suggested the glycosylation of PSA to be a promising marker for a more specific yet non-invasive PCa diagnosis. Recent studies on the molecular features of PSA glycosylation (such as antenna modification and core fucosylation) were not successful in demonstrating its potential for an improved PCa diagnosis, probably due to the lack of analytical sensitivity and specificity of the applied assays. In this study, we established for the first time a high-performance PSA Glycomics Assay (PGA), allowing differentiation of α2,6- and α2,3-sialylated isomers, the latter one being suggested to be a hallmark of aggressive types of cancer. After affinity purification from urine and tryptic digestion, PSA samples were analyzed by CE-ESI-MS (capillary electrophoresis - electrospray ionization coupled to mass spectrometry). Based on positive controls, an average inter-day relative standard deviation of 14% for 41 N-glycopeptides was found. The assay was further verified by analyzing PSA captured from patients' urine samples. A total of 67 N-glycopeptides were identified from the PSA pooled from the patients. In summary, the first PGA successfully established in this study allows an in-depth relative quantitation of PSA glycoforms from urine. The PGA is a promising tool for the determination of potential glycomic biomarkers for the differentiation between aggressive PCa, indolent PCa and benign prostate hyperplasia in larger cohort studies.

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