Histone deacetylase 10-promoted autophagy as a druggable point of interference to improve the treatment response of advanced neuroblastomas

Neuroblastoma is the most common extracranial solid tumor in childhood. Despite intense multimodal therapy and many improvements through basic scientific and clinical research, the successful response of advanced-stage patients to chemotherapy remains poor. Autophagy is a cytoprotective mechanism th...

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Bibliographic Details
Main Authors: Oehme, Ina (Author) , Lodrini, Marco (Author) , Brady, Nathan (Author) , Witt, Olaf (Author)
Format: Article (Journal)
Language:English
Published: 08 Oct 2013
In: Autophagy
Year: 2013, Volume: 9, Issue: 12, Pages: 2163-2165
ISSN:1554-8635
DOI:10.4161/auto.26450
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.4161/auto.26450
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Author Notes:Ina Oehme, Marco Lodrini, Nathan R Brady, and Olaf Witt
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Summary:Neuroblastoma is the most common extracranial solid tumor in childhood. Despite intense multimodal therapy and many improvements through basic scientific and clinical research, the successful response of advanced-stage patients to chemotherapy remains poor. Autophagy is a cytoprotective mechanism that may help advanced cancer cells survive stressful conditions such as chemotherapy. Here we review our recent findings describing HDAC10 as a promoter of autophagy-mediated survival in neuroblastoma cells and identifying this HDAC isozyme as a druggable regulator of advanced-stage tumor cell survival. These results propose a new and promising way to considerably improve treatment response in the neuroblastoma patient subgroup with the poorest outcome.
Item Description:Gesehen am 29.11.2021
Physical Description:Online Resource
ISSN:1554-8635
DOI:10.4161/auto.26450