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Preventing inflammation inhibits biopsy-mediated changes in tumor cell behavior.
Alieva, Maria; Margarido, Andreia S; Wieles, Tamara; Abels, Erik R; Colak, Burcin; Boquetale, Carla; Jan Noordmans, Herke; Snijders, Tom J; Broekman, Marike L; van Rheenen, Jacco.
Afiliación
  • Alieva M; Cancer Genomics Netherlands, Hubrecht Institute-KNAW & University Medical Center Utrecht, Uppsalalaan 8, 3584CT, Utrecht, The Netherlands.
  • Margarido AS; Cancer Genomics Netherlands, Hubrecht Institute-KNAW & University Medical Center Utrecht, Uppsalalaan 8, 3584CT, Utrecht, The Netherlands.
  • Wieles T; Cancer Genomics Netherlands, Hubrecht Institute-KNAW & University Medical Center Utrecht, Uppsalalaan 8, 3584CT, Utrecht, The Netherlands.
  • Abels ER; Departments of Neurology, Massachusetts General Hospital, Harvard Medical School, 149 13th Street, Boston, MA, 02129, USA.
  • Colak B; Cancer Genomics Netherlands, Hubrecht Institute-KNAW & University Medical Center Utrecht, Uppsalalaan 8, 3584CT, Utrecht, The Netherlands.
  • Boquetale C; Cancer Genomics Netherlands, Hubrecht Institute-KNAW & University Medical Center Utrecht, Uppsalalaan 8, 3584CT, Utrecht, The Netherlands.
  • Jan Noordmans H; Medical Technology and Clinical Physics, University Medical Center Utrecht, Heidelberglaan 100, 3584 CX, Utrecht, The Netherlands.
  • Snijders TJ; Department of Neurology & Neurosurgery, Brain Center Rudolf Magnus, University Medical Center Utrecht, Heidelberglaan 100, 3584 CX, Utrecht, The Netherlands.
  • Broekman ML; Departments of Neurology, Massachusetts General Hospital, Harvard Medical School, 149 13th Street, Boston, MA, 02129, USA.
  • van Rheenen J; Department of Neurology & Neurosurgery, Brain Center Rudolf Magnus, University Medical Center Utrecht, Heidelberglaan 100, 3584 CX, Utrecht, The Netherlands.
Sci Rep ; 7(1): 7529, 2017 08 08.
Article en En | MEDLINE | ID: mdl-28790339
ABSTRACT
Although biopsies and tumor resection are prognostically beneficial for glioblastomas (GBM), potential negative effects have also been suggested. Here, using retrospective study of patients and intravital imaging of mice, we identify some of these negative aspects, including stimulation of proliferation and migration of non-resected tumor cells, and provide a strategy to prevent these adverse effects. By repeated high-resolution intravital microscopy, we show that biopsy-like injury in GBM induces migration and proliferation of tumor cells through chemokine (C-C motif) ligand 2 (CCL-2)-dependent recruitment of macrophages. Blocking macrophage recruitment or administrating dexamethasone, a commonly used glucocorticoid to prevent brain edema in GBM patients, suppressed the observed inflammatory response and subsequent tumor growth upon biopsy both in mice and in multifocal GBM patients. Taken together, our study suggests that inhibiting CCL-2-dependent recruitment of macrophages may further increase the clinical benefits from surgical and biopsy procedures.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / Dexametasona / Regulación Neoplásica de la Expresión Génica / Glioblastoma / Antineoplásicos Hormonales / Macrófagos / Antiinflamatorios Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies Idioma: En Revista: Sci Rep Año: 2017 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / Dexametasona / Regulación Neoplásica de la Expresión Génica / Glioblastoma / Antineoplásicos Hormonales / Macrófagos / Antiinflamatorios Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies Idioma: En Revista: Sci Rep Año: 2017 Tipo del documento: Article País de afiliación: Países Bajos