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Nuclear Glycoprotein A Repetitions Predominant (GARP) Is a Common Trait of Glioblastoma Stem-like Cells and Correlates with Poor Survival in Glioblastoma Patients.
Zimmer, Niklas; Trzeciak, Emily R; Müller, Andreas; Licht, Philipp; Sprang, Bettina; Leukel, Petra; Mailänder, Volker; Sommer, Clemens; Ringel, Florian; Tuettenberg, Jochen; Kim, Ella; Tuettenberg, Andrea.
Afiliación
  • Zimmer N; Department of Dermatology, University Medical Center Mainz, 55131 Mainz, Germany.
  • Trzeciak ER; Department of Dermatology, University Medical Center Mainz, 55131 Mainz, Germany.
  • Müller A; Department of Neurosurgery, University Medical Center Mainz, 55131 Mainz, Germany.
  • Licht P; Laboratory of Experimental Neurooncology, University Medical Center Mainz, 55131 Mainz, Germany.
  • Sprang B; Department of Dermatology, University Medical Center Mainz, 55131 Mainz, Germany.
  • Leukel P; Department of Neurosurgery, University Medical Center Mainz, 55131 Mainz, Germany.
  • Mailänder V; Laboratory of Experimental Neurooncology, University Medical Center Mainz, 55131 Mainz, Germany.
  • Sommer C; Institute of Neuropathology, University Medical Center Mainz, 55131 Mainz, Germany.
  • Ringel F; Department of Dermatology, University Medical Center Mainz, 55131 Mainz, Germany.
  • Tuettenberg J; Research Center for Immunotherapy, University Medical Center Mainz, 55131 Mainz, Germany.
  • Kim E; Institute of Neuropathology, University Medical Center Mainz, 55131 Mainz, Germany.
  • Tuettenberg A; Department of Neurosurgery, University Medical Center Mainz, 55131 Mainz, Germany.
Cancers (Basel) ; 15(24)2023 Dec 05.
Article en En | MEDLINE | ID: mdl-38136258
ABSTRACT
Glioblastoma (GB) is notoriously resistant to therapy. GB genesis and progression are driven by glioblastoma stem-like cells (GSCs). One goal for improving treatment efficacy and patient outcomes is targeting GSCs. Currently, there are no universal markers for GSCs. Glycoprotein A repetitions predominant (GARP), an anti-inflammatory protein expressed by activated regulatory T cells, was identified as a possible marker for GSCs. This study evaluated GARP for the detection of human GSCs utilizing a multidimensional experimental design that replicated several features of GB (1) intratumoral heterogeneity, (2) cellular hierarchy (GSCs with varied degrees of self-renewal and differentiation), and (3) longitudinal GSC evolution during GB recurrence (GSCs from patient-matched newly diagnosed and recurrent GB). Our results indicate that GARP is expressed by GSCs across various cellular states and disease stages. GSCs with an increased GARP expression had reduced self-renewal but no alterations in proliferative capacity or differentiation commitment. Rather, GARP correlated inversely with the expression of GFAP and PDGFR-α, markers of astrocyte or oligodendrocyte differentiation. GARP had an abnormal nuclear localization (GARPNU+) in GSCs and was negatively associated with patient survival. The uniformity of GARP/GARPNU+ expression across different types of GSCs suggests a potential use of GARP as a marker to identify GSCs.
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Texto completo: 1 Colección: 01-internacional Idioma: En Revista: Cancers (Basel) Año: 2023 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Idioma: En Revista: Cancers (Basel) Año: 2023 Tipo del documento: Article País de afiliación: Alemania