Gliomasphere marker combinatorics: multidimensional flow cytometry detects CD44+/CD133+/ITGA6+/CD36+ signature

  • F Erhart
  • , B Blauensteiner
  • , G Zirkovits
  • , D Printz
  • , K Soukup
  • , S Klingenbrunner
  • , K Fischhuber
  • , R Reitermaier
  • , Angela Halfmann
  • , Daniela Lötsch
  • , Sabine Spiegl-Kreinecker
  • , Walter Berger
  • , Carmen Visus
  • , Alexander Dohnal

Research output: Contribution to journalArticlepeer-review

Abstract

Glioblastoma is the most dangerous brain cancer. One reason for glioblastoma's aggressiveness are glioblastoma stem-like cells. To target them, a number of markers have been proposed (CD133, CD44, CD15, A2B5, CD36, CXCR4, IL6R, L1CAM, and ITGA6). A comprehensive study of co-expression patterns of them has, however, not been performed so far. Here, we mapped the multidimensional co-expression profile of these stemness-associated molecules. Gliomaspheres - an established model of glioblastoma stem-like cells - were used. Seven different gliomasphere systems were subjected to multicolor flow cytometry measuring the nine markers CD133, CD44, CD15, A2B5, CD36, CXCR4, IL6R, L1CAM, and ITGA6 all simultaneously based on a novel 9-marker multicolor panel developed for this study. The viSNE dimensionality reduction algorithm was applied for analysis. All gliomaspheres were found to express at least five different glioblastoma stem-like cell markers. Multi-dimensional analysis showed that all studied gliomaspheres consistently harbored a cell population positive for the molecular signature CD44+/CD133+/ITGA6+/CD36+. Glioblastoma patients with an enrichment of this combination had a significantly worse survival outcome when analyzing the two largest available The Cancer Genome Atlas datasets (MIT/Harvard Affymetrix: P = 0.0015, University of North Carolina Agilent: P = 0.0322). In sum, we detected a previously unknown marker combination - demonstrating feasibility, usefulness, and importance of high-dimensional gliomasphere marker combinatorics.
Original languageEnglish
Pages (from-to)281-92
Number of pages12
JournalJournal of Cellular and Molecular Medicine
Issue number1
DOIs
Publication statusPublished - 2019

Fields of science

  • 302 Clinical Medicine

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