Cancer Science · 2011 · 183 citations · 30 references
MedicineCancer BiologyOncologyAutophagyCancer PharmacologyMolecular OncologyAutophagy In CancerAutophagy ModulationAutophagy RegulationBrain TumorsCancer Cell SignalingGlioblastomaCancer-associated AutophagyDifferentiationGlioblastoma Recurrence MechanismsGlioblastoma Tumor BiologyPro-tumorigenic SignalingTherapeutic Target Identification
Glioblastoma (GBM) is a highly aggressive brain tumor characterized by increased proliferation and resistance to chemotherapy and radiotherapy. Recently, a growing body of evidence suggests that glioma-initiating cells (GICs) are responsible for the initiation and recurrence of GBM. However, the factors determining the differential development of GICs remain poorly defined. In the present study, we show that curcumin, a natural compound with low toxicity in normal cells, significantly induced differentiation of GICs in vivo and in vitro by inducing autophagy. Moreover, curcumin also suppressed tumor formation on intracranial GICs implantation into mice. Our results suggest that autophagy plays an essential role in the regulation of GIC self-renewal, differentiation, and tumorigenic potential, suggesting autophagy could be a promising therapeutic target in a subset of glioblastomas. This is the first evidence that curcumin has differentiating and tumor-suppressing actions on GICs.
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