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024 7 _ |a 10.1158/0008-5472.CAN-13-1904
|2 doi
024 7 _ |a pmid:24419085
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024 7 _ |a 0008-5472
|2 ISSN
024 7 _ |a 0099-7013
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024 7 _ |a 0099-7374
|2 ISSN
024 7 _ |a 1538-7445
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024 7 _ |a altmetric:2045376
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037 _ _ |a DKFZ-2017-00507
041 _ _ |a eng
082 _ _ |a 610
100 1 _ |a Fabian, Johannes
|0 P:(DE-HGF)0
|b 0
|e First author
245 _ _ |a GRHL1 acts as tumor suppressor in neuroblastoma and is negatively regulated by MYCN and HDAC3.
260 _ _ |a Philadelphia, Pa.
|c 2014
|b AACR
336 7 _ |a article
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336 7 _ |a Journal Article
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|s 1490273091_30686
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336 7 _ |a ARTICLE
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336 7 _ |a Journal Article
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520 _ _ |a Neuroblastoma is an embryonic solid tumor of neural crest origin and accounts for 11% of all cancer-related deaths in children. Novel therapeutic strategies are therefore urgently required. MYCN oncogene amplification, which occurs in 20% of neuroblastomas, is a hallmark of high risk. Here, we aimed to exploit molecular mechanisms that can be pharmacologically addressed with epigenetically modifying drugs, such as histone deacetylase (HDAC) inhibitors. Grainyhead-like 1 (GRHL1), a gene critical for Drosophila neural development, belonged to the genes most strongly responding to HDAC inhibitor treatment of neuroblastoma cells in a genome-wide screen. An increase in the histone H4 pan-acetylation associated with its promoter preceded transcriptional activation. Physically adjacent, HDAC3 and MYCN colocalized to the GRHL1 promoter and repressed its transcription. High-level GRHL1 expression in primary neuroblastomas correlated on transcriptional and translational levels with favorable patient survival and established clinical and molecular markers for favorable tumor biology, including lack of MYCN amplification. Enforced GRHL1 expression in MYCN-amplified neuroblastoma cells with low endogenous GRHL1 levels abrogated anchorage-independent colony formation, inhibited proliferation, and retarded xenograft growth in mice. GRHL1 knockdown in MYCN single-copy cells with high endogenous GRHL1 levels promoted colony formation. GRHL1 regulated 170 genes genome-wide, and most were involved in pathways regulated during neuroblastomagenesis, including nervous system development, proliferation, cell-cell adhesion, cell spreading, and cellular differentiation. In summary, the data presented here indicate a significant role of HDAC3 in the MYCN-mediated repression of GRHL1 and suggest drugs that block HDAC3 activity and suppress MYCN expression as promising candidates for novel treatment strategies of high-risk neuroblastoma.
536 _ _ |a 317 - Translational cancer research (POF3-317)
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650 _ 7 |a Antineoplastic Agents
|2 NLM Chemicals
650 _ 7 |a GRHL1 protein, human
|2 NLM Chemicals
650 _ 7 |a Histone Deacetylase Inhibitors
|2 NLM Chemicals
650 _ 7 |a Hydroxamic Acids
|2 NLM Chemicals
650 _ 7 |a Indoles
|2 NLM Chemicals
650 _ 7 |a MYCN protein, human
|2 NLM Chemicals
650 _ 7 |a N-Myc Proto-Oncogene Protein
|2 NLM Chemicals
650 _ 7 |a Nuclear Proteins
|2 NLM Chemicals
650 _ 7 |a Oncogene Proteins
|2 NLM Chemicals
650 _ 7 |a Repressor Proteins
|2 NLM Chemicals
650 _ 7 |a panobinostat
|0 9647FM7Y3Z
|2 NLM Chemicals
650 _ 7 |a Histone Deacetylases
|0 EC 3.5.1.98
|2 NLM Chemicals
650 _ 7 |a histone deacetylase 3
|0 EC 3.5.1.98
|2 NLM Chemicals
700 1 _ |a Lodrini, Marco
|0 P:(DE-HGF)0
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700 1 _ |a Oehme, Ina
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700 1 _ |a Schier, Marie C
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700 1 _ |a Thole, Theresa
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700 1 _ |a Hielscher, Thomas
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700 1 _ |a Kopp-Schneider, Annette
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700 1 _ |a Opitz, Lennart
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700 1 _ |a Capper, David
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700 1 _ |a von Deimling, Andreas
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700 1 _ |a Wiegand, Inga
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700 1 _ |a Milde, Till
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700 1 _ |a Mahlknecht, Ulrich
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700 1 _ |a Westermann, Frank
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700 1 _ |a Popanda, Odilia
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700 1 _ |a Roels, Frederik
|b 15
700 1 _ |a Hero, Barbara
|b 16
700 1 _ |a Berthold, Frank
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700 1 _ |a Fischer, Matthias
|b 18
700 1 _ |a Kulozik, Andreas E
|b 19
700 1 _ |a Witt, Olaf
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700 1 _ |a Deubzer, Hedwig E
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773 _ _ |a 10.1158/0008-5472.CAN-13-1904
|g Vol. 74, no. 9, p. 2604 - 2616
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