Abstract

BackgroundAberrant Hedgehog (Hh) signaling is often associated with neuroblastoma (NB), a childhood malignancy with varying clinical outcomes due to different molecular characteristics. Inhibition of Hh signaling with small molecule inhibitors, particularly with GANT-61, significantly suppresses NB growth. However, NB with MYCN amplification is less sensitive to GANT-61 than those without MYCN amplification.MethodsAutophagic process was examined in two MYCN amplified and two MYCN non-amplified NB cells treated with GANT-61. Subsequently, chemical and genetic approaches were applied with GANT-61 together to evaluate the role of autophagy in GANT-61 induced cell death.ResultsHere we show that GANT-61 enhanced autophagy in MYCN amplified NB cells. Both an autophagic inhibitor 3-methyladenine (3-MA) and genetic disruption of ATG5 or ATG7 expression suppressed GANT-61 induced autophagy and significantly increased apoptotic cell death, whereas pre-treatment with an apoptotic inhibitor, Z-VAD-FMK, rescued GANT-61 induced cell death and had no effect on the autophagic process. In the other hand, GANT-61 barely induced autophagy in MYCN non-amplified NB cells, but overexpression of MYCN in MYCN non-amplified NB cells recapitulated GANT-61 induced autophagy seen in MYCN amplified NB cells, suggesting that the level of GANT-61 induced autophagy in NB cells is related to MYCN expression level in cells.ConclusionAberrant Hh signaling activation as an oncogenic driver in NB renders inhibition of Hh signaling an effective measure to suppress NB growth. However, our data suggest that enhanced autophagy concomitant with Hh signaling inhibition acts as a pro-survival factor to maintain cell viability, which reduces GANT-61 efficacy. Besides, MYCN amplification is likely involved in the induction of the pro-survival autophagy. Overall, simultaneous inhibition of both Hh signaling and autophagy could be a better way to treat MYCN amplified NB.Electronic supplementary materialThe online version of this article (doi:10.1186/1471-2407-14-768) contains supplementary material, which is available to authorized users.

Highlights

  • Aberrant Hedgehog (Hh) signaling is often associated with neuroblastoma (NB), a childhood malignancy with varying clinical outcomes due to different molecular characteristics

  • We found that the autophagic level in MYCN non-amplified NB cells was hardly affected by GANT-61, but MYCN overexpression in MYCN nonamplified NB cells could enhance GANT-61 induced autophagy, suggesting that MYCN amplification has a positive role in the induction of the pro-survival autophagy

  • GANT-61 decreases cell viability and induce apoptosis in MYCN amplified NB cells GANT-61, an inhibitor of Hh signaling effector GLI protein, was reported to have a cytotoxic effect on NB cell lines, such as SK-N-AS, SH-SY5Y, SK-N-DZ etc., and GANT-61 efficacy is reversely correlated with MYCN expression [16]

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Summary

Introduction

Aberrant Hedgehog (Hh) signaling is often associated with neuroblastoma (NB), a childhood malignancy with varying clinical outcomes due to different molecular characteristics. Inhibition of Hh signaling with small molecule inhibitors, with GANT-61, significantly suppresses NB growth. NB is one of the most common solid malignant tumors in children. It arises from neural crest element of the sympathetic nervous system and usually occurs in the adrenal medulla [1]. Half neuroblastoma is classified as highrisk group due to aggressive tumor and poor prognosis. Children with high-risk tumor are aggressively treated with multi-modal therapy, this group still has poor survival rate (40%-50%) [3]. It is critical to understand the underlying therapy-resistant mechanism of high-risk tumor

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