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Neuroblastoma cells depend on HDAC11 for mitotic cell cycle progression and survival

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Item Type:Article
Title:Neuroblastoma cells depend on HDAC11 for mitotic cell cycle progression and survival
Creators Name:Thole, T.M. and Lodrini, M. and Fabian, J. and Wuenschel, J. and Pfeil, S. and Hielscher, T. and Kopp-Schneider, A. and Heinicke, U. and Fulda, S. and Witt, O. and Eggert, A. and Fischer, M. and Deubzer, H.E.
Abstract:The number of long-term survivors of high-risk neuroblastoma remains discouraging, with 10-year survival as low as 20%, despite decades of considerable international efforts to improve outcome. Major obstacles remain and include managing resistance to induction therapy, which causes tumor progression and early death in high-risk patients, and managing chemotherapy-resistant relapses, which can occur years after the initial diagnosis. Identifying and validating novel therapeutic targets is essential to improve treatment. Delineating and deciphering specific functions of single histone deacetylases in neuroblastoma may support development of targeted acetylome-modifying therapeutics for patients with molecularly defined high-risk neuroblastoma profiles. We show here that HDAC11 depletion in MYCN-driven neuroblastoma cell lines strongly induces cell death, mostly mediated by apoptotic programs. Genes necessary for mitotic cell cycle progression and cell division were most prominently enriched in at least two of three time points in whole-genome expression data combined from two cell systems, and all nine genes in these functional categories were strongly repressed, including CENPA, KIF14, KIF23 and RACGAP1. Enforced expression of one selected candidate, RACGAP1, partially rescued the induction of apoptosis caused by HDAC11 depletion. High-level expression of all nine genes in primary neuroblastomas significantly correlated with unfavorable overall and event-free survival in patients, suggesting a role in mediating the more aggressive biological and clinical phenotype of these tumors. Our study identified a group of cell cycle-promoting genes regulated by HDAC11, being both predictors of unfavorable patient outcome and essential for tumor cell viability. The data indicate a significant role of HDAC11 for mitotic cell cycle progression and survival of MYCN-amplified neuroblastoma cells, and suggests that HDAC11 could be a valuable drug target.
Keywords:Apoptosis, Cdc Genes, Cell Cycle, Cell Survival, Disease-Free Survival, Gene Expression, Histone Deacetylases, Local Neoplasm Recurrence, Mitosis, Neuroblastoma, Tumor Cell Line
Source:Cell Death & Disease
ISSN:2041-4889
Publisher:Nature Publishing Group (U.K.)
Volume:8
Number:3
Page Range:e2635
Date:2 March 2017
Official Publication:https://doi.org/10.1038/cddis.2017.49
PubMed:View item in PubMed

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