Neuroblastomas are pediatric tumours originating from neuroblasts in the developing peripheral nervous system. The neurotrophin BDNF is a key regulator of survival and differentiation of specific neuronal populations in the central and peripheral nervous system. Patients whose neuroblastoma tumors express high levels of BDNF and TrkB have an unfavorable prognosis.We have previously reported on the neuronal differentiating activity of PPAR²/´ natural and synthetic ligands by modulating BDNF/TrkB pathway, suggesting their potential use as new therapeutic strategies for neuroblastoma.. The validation of new therapeutic agents implies the understanding of their mechanisms of action. Herein, we report the effects of activated-PPAR²/´ on signal transduction pathways known to be involved in neuronal differentiation, such as ERK1,2 and BDNF pathways. The results obtained, using also PPAR²/´ silencing, indicating a neuronal differentiating effect PPAR²/´-dependent through BDNF-P75-ERK1,2 pathways, further support a role for PPAR²/´ in neuronal differentiation and pointing towards PPAR²/´ as modulator of pathways crucial for neuronal differentiation. These findings open new perspectives in the formulation of potential therapeutic approaches to be used as adjuvant treatment with the standard therapies.
Signal transduction pathways involved in pparß/´-induced neuronal differentiation.
Di Loreto S;
2011
Abstract
Neuroblastomas are pediatric tumours originating from neuroblasts in the developing peripheral nervous system. The neurotrophin BDNF is a key regulator of survival and differentiation of specific neuronal populations in the central and peripheral nervous system. Patients whose neuroblastoma tumors express high levels of BDNF and TrkB have an unfavorable prognosis.We have previously reported on the neuronal differentiating activity of PPAR²/´ natural and synthetic ligands by modulating BDNF/TrkB pathway, suggesting their potential use as new therapeutic strategies for neuroblastoma.. The validation of new therapeutic agents implies the understanding of their mechanisms of action. Herein, we report the effects of activated-PPAR²/´ on signal transduction pathways known to be involved in neuronal differentiation, such as ERK1,2 and BDNF pathways. The results obtained, using also PPAR²/´ silencing, indicating a neuronal differentiating effect PPAR²/´-dependent through BDNF-P75-ERK1,2 pathways, further support a role for PPAR²/´ in neuronal differentiation and pointing towards PPAR²/´ as modulator of pathways crucial for neuronal differentiation. These findings open new perspectives in the formulation of potential therapeutic approaches to be used as adjuvant treatment with the standard therapies.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
