001     126989
005     20240228135028.0
024 7 _ |a 10.1002/ijc.28719
|2 doi
024 7 _ |a pmid:24420698
|2 pmid
024 7 _ |a 0020-7136
|2 ISSN
024 7 _ |a 1097-0215
|2 ISSN
037 _ _ |a DKFZ-2017-03015
041 _ _ |a eng
082 _ _ |a 610
100 1 _ |a Kerl, Kornelius
|b 0
245 _ _ |a Arsenic trioxide inhibits tumor cell growth in malignant rhabdoid tumors in vitro and in vivo by targeting overexpressed Gli1.
260 _ _ |a Bognor Regis
|c 2014
|b Wiley-Liss
336 7 _ |a article
|2 DRIVER
336 7 _ |a Output Types/Journal article
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336 7 _ |a Journal Article
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|m journal
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|s 1506000063_16804
|2 PUB:(DE-HGF)
336 7 _ |a ARTICLE
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336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a Journal Article
|0 0
|2 EndNote
520 _ _ |a Rhabdoid tumors are highly aggressive tumors occurring in infants and very young children. Despite multimodal and intensive therapy prognosis remains poor. Molecular analyses have uncovered several deregulated pathways, among them the CDK4/6-Rb-, the WNT- and the Sonic hedgehog (SHH) pathways. The SHH pathway is activated in rhabdoid tumors by GLI1 overexpression. Here, we demonstrate that arsenic trioxide (ATO) inhibits tumor cell growth of malignant rhabdoid tumors in vitro and in a mouse xenograft model by suppressing Gli1. Our data uncover ATO as a promising therapeutic approach to improve prognosis for rhabdoid tumor patients.
536 _ _ |a 312 - Functional and structural genomics (POF3-312)
|0 G:(DE-HGF)POF3-312
|c POF3-312
|f POF III
|x 0
588 _ _ |a Dataset connected to CrossRef, PubMed,
650 _ 7 |a Antineoplastic Agents
|2 NLM Chemicals
650 _ 7 |a Arsenicals
|2 NLM Chemicals
650 _ 7 |a GLI1 protein, human
|2 NLM Chemicals
650 _ 7 |a Gli protein, mouse
|2 NLM Chemicals
650 _ 7 |a Hedgehog Proteins
|2 NLM Chemicals
650 _ 7 |a Kruppel-Like Transcription Factors
|2 NLM Chemicals
650 _ 7 |a Oxides
|2 NLM Chemicals
650 _ 7 |a SHH protein, human
|2 NLM Chemicals
650 _ 7 |a Transcription Factors
|2 NLM Chemicals
650 _ 7 |a Zinc Finger Protein GLI1
|2 NLM Chemicals
650 _ 7 |a arsenic trioxide
|0 S7V92P67HO
|2 NLM Chemicals
700 1 _ |a Moreno, Natalia
|b 1
700 1 _ |a Holsten, Till
|b 2
700 1 _ |a Ahlfeld, Julia
|b 3
700 1 _ |a Mertins, Julius
|b 4
700 1 _ |a Hotfilder, Marc
|b 5
700 1 _ |a Kool, Marcel
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|u dkfz
700 1 _ |a Bartelheim, Kerstin
|b 7
700 1 _ |a Schleicher, Sabine
|b 8
700 1 _ |a Handgretinger, Rupert
|b 9
700 1 _ |a Schüller, Ulrich
|b 10
700 1 _ |a Meisterernst, Michael
|b 11
700 1 _ |a Frühwald, Michael C
|b 12
773 _ _ |a 10.1002/ijc.28719
|g Vol. 135, no. 4, p. 989 - 995
|0 PERI:(DE-600)1474822-8
|n 4
|p 989 - 995
|t International journal of cancer
|v 135
|y 2014
|x 0020-7136
909 C O |o oai:inrepo02.dkfz.de:126989
|p VDB
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
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|b 6
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913 1 _ |a DE-HGF
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|v Functional and structural genomics
|x 0
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|3 G:(DE-HGF)POF3
|b Gesundheit
914 1 _ |y 2014
915 _ _ |a Nationallizenz
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|x 0
980 _ _ |a journal
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980 _ _ |a I:(DE-He78)B062-20160331
980 _ _ |a UNRESTRICTED


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