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dc.contributor.authorBrett-Morris, A
dc.contributor.authorWright, BM
dc.contributor.authorSeo, Y
dc.contributor.authorPasupuleti, V
dc.contributor.authorZhang, J
dc.contributor.authorLu, J
dc.contributor.authorSpina, R
dc.contributor.authorBar, EE
dc.contributor.authorGujrati, M
dc.contributor.authorSchur, R
dc.contributor.authorLu, ZR
dc.contributor.authorWelford, SM
dc.date.accessioned2015-02-10T00:52:46Z
dc.date.available2015-02-10T00:52:46Z
dc.date.copyright2014-10-02
dc.identifier.citationCancer Res December 1, 2014 74; 6925
dc.identifier.issn1538-7445
dc.identifier.urihttp://hdl.handle.net/10292/8389
dc.description.abstractGlioblastoma multiforme (GBM) is the most common and severe form of brain cancer. The median survival time of patients is approximately 12 months due to poor responses to surgery and chemoradiation. To understand the mechanisms involved in radioresistance, we conducted a genetic screen using an shRNA library to identify genes in which inhibition would sensitize cells to radiation. The results were cross-referenced with the Oncomine and Rembrandt databases to focus on genes that are highly expressed in GBM tumors and associated with poor patient outcomes. Spermidine/spermine-N1-acetyltransferase 1 (SAT1), an enzyme involved in polyamine catabolism, was identified as a gene that promotes resistance to ionizing radiation (IR), is overexpressed in brain tumors, and correlates with poor outcomes. Knockdown of SAT1 using shRNA and siRNA approaches in multiple cell and neurosphere lines resulted in sensitization of GBM cells to radiation in colony formation assays and tumors, and decreased tumorigenesis in vivo. Radiosensitization occurred specifically in G2-M and S phases, suggesting a role for SAT1 in homologous recombination (HR) that was confirmed in a DR-GFP reporter system. Mechanistically, we found that SAT1 promotes acetylation of histone H3, suggesting a new role of SAT1 in chromatin remodeling and regulation of gene expression. In particular, SAT1 depletion led to a dramatic reduction in BRCA1 expression, explaining decreased HR capacity. Our findings suggest that the biologic significance of elevated SAT1 expression in GBM lies in its contribution to cell radioresistance and that SAT1 may potentially be a therapeutic target to sensitize GBM to cancer therapies. Cancer Res; 74(23); 1-10. ©2014 AACR.
dc.languageENG
dc.publisherAmerican Association for Cancer Research (AACR)
dc.relation.urihttp://dx.doi.org/10.1158/0008-5472.CAN-14-1249
dc.rightsAuthors final version may be deposited on institutional website or institutional repository if required by institution. Published source must be acknowledged. Must link to the publisher PDF of article on journal website
dc.titleThe polyamine catabolic enzyme SAT1 modulates tumorigenesis and radiation response in GBM
dc.typeJournal Article
dc.rights.accessrightsOpenAccess
dc.identifier.doi10.1158/0008-5472.CAN-14-1249
pubs.elements-id173686


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