Glycomic Approach for Potential Biomarkers on Prostate Cancer: Profiling of N‐Linked Glycans in Human Sera and pRNS Cell Lines
Author(s) -
Maria Lorna A. De Leoz,
Hyun Joo An,
Scott Kronewitter,
JaeHan Kim,
Sean Beecroft,
Ruth L. Vinall,
Suzanne Miyamoto,
Ralph de Vere White,
Kit S. Lam,
Carlito B. Lebrilla
Publication year - 2008
Publication title -
disease markers
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.912
H-Index - 66
eISSN - 1875-8630
pISSN - 0278-0240
DOI - 10.1155/2008/515318
Subject(s) - prostate cancer , profiling (computer programming) , glycan , computational biology , cancer cell lines , glycomics , biology , medicine , cancer , cancer cell , genetics , computer science , glycoprotein , operating system
Prostate cancer is a leading cause of cancer death among men. Currently available screening test measures prostate-specific antigen (PSA) to detect prostate cancer. However, this test produces false positive values that often lead to negative biopsies. Therefore, a more reliable diagnostic tool is needed. Glycans in serum are of particular interest as around half of all proteins are glycosylated. In this study, N-linked glycans were enzymatically released by PNGase F from prostate epithelial cell lines (pRNS) expressing wild type or mutant androgen receptors and a small set of human serum samples. Released glycans were purified and partitioned into neutral and acidic components by solid phase extraction (SPE) using graphitized carbon cartridges. The SPE fractions were analyzed by matrix-assisted laser desorption/ionization Fourier transform ion cyclotron resonance mass spectrometry (MALDI FT-ICR MS). Significant changes in some high-mannose and fucosylated biantennary complex N-linked glycans were observed in the serum of prostate cancer patients.
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