Identification of Plasma Membrane Glycoproteins Specific to Human Glioblastoma Multiforme Cells Using Lectin Arrays and LC‐MS/MS

• Published in: Proteomics (Weinheim) 2018-01, Vol.18 (1), p.n/a
• Main Authors: Park, Yae Eun, Yeom, Jeonghun, Kim, YoungSoo, Lee, Hye Jin, Han, Ki‐Cheol, Lee, Seung‐Taek, Lee, Cheolju, Lee, Ji Eun
• Format: Article
• Language: English
• Subjects: Biomarkers, Tumor - metabolism; Brain; Brain cancer; Brain Neoplasms - metabolism; Brain Neoplasms - pathology; Carbohydrates; Cell Membrane - metabolism; Cell surface; cell surface glycoprotein; Chromatography, Liquid - methods; Columns (structural); Diagnostic systems; Glioblastoma; Glioblastoma - metabolism; Glioblastoma - pathology; Glioblastoma multiforme; glioblastoma multiforme (GBM); Glioma cells; Glycoproteins; Glycosylation; Humans; Invasiveness; label‐free quantitative MS; lectin arrays; Lectins; Lectins - metabolism; Markers; Medical prognosis; Membrane glycoproteins; Membrane Glycoproteins - metabolism; Oligodendroglioma; Oligodendroglioma cells; Proteins; Quantitative analysis; Surface markers; Tandem Mass Spectrometry - methods; Tumor cells; Tumor Cells, Cultured
• ISSN: 1615-9853; 1615-9861
• DOI: 10.1002/pmic.201700302

Glioblastoma, also known as glioblastoma multiforme (GBM), is the most malignant type of brain cancer and has poor prognosis with a median survival of less than one year. While the structural changes of tumor cell surface carbohydrates are known to be associated with invasive behavior of tumor cells, the cell surface glycoproteins to differentiate the low‐ and high‐grade glioma cells can be potential diagnostic markers and therapeutic targets for GBMs. In the present study, lectin arrays consisting of eight lectins were employed to explore cell surface carbohydrate expression patterns on low‐grade oligodendroglioma cells (Hs683) and GBM cells (T98G). Griffonia simplicifolia I (GS I) was found to selectively bind to T98G cells and not to Hs683 cells. For identification of the glioblastoma‐specific cell surface markers, the glycoproteins from each cell type were captured by a GS I lectin column and analyzed by LC‐MS/MS. The identified proteins from the two cell types were quantified using label‐free quantitative analysis based on spectral counting. Of cell surface glycoproteins showing significant increases in T98G cells, five proteins were selected for verification of both protein and glycosylation level changes using Western blot and GS I lectin‐based immunosorbent assay.