001     144001
005     20240229112613.0
024 7 _ |a 10.1016/j.stem.2019.05.013
|2 doi
024 7 _ |a pmid:31204176
|2 pmid
024 7 _ |a 1875-9777
|2 ISSN
024 7 _ |a 1934-5909
|2 ISSN
024 7 _ |a altmetric:62031570
|2 altmetric
037 _ _ |a DKFZ-2019-01552
041 _ _ |a eng
082 _ _ |a 570
100 1 _ |a Huang, Miller
|b 0
245 _ _ |a Engineering Genetic Predisposition in Human Neuroepithelial Stem Cells Recapitulates Medulloblastoma Tumorigenesis.
260 _ _ |a Amsterdam [u.a.]
|c 2019
|b Elsevier
336 7 _ |a article
|2 DRIVER
336 7 _ |a Output Types/Journal article
|2 DataCite
336 7 _ |a Journal Article
|b journal
|m journal
|0 PUB:(DE-HGF)16
|s 1569402422_659
|2 PUB:(DE-HGF)
336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a Journal Article
|0 0
|2 EndNote
520 _ _ |a Human neural stem cell cultures provide progenitor cells that are potential cells of origin for brain cancers. However, the extent to which genetic predisposition to tumor formation can be faithfully captured in stem cell lines is uncertain. Here, we evaluated neuroepithelial stem (NES) cells, representative of cerebellar progenitors. We transduced NES cells with MYCN, observing medulloblastoma upon orthotopic implantation in mice. Significantly, transcriptomes and patterns of DNA methylation from xenograft tumors were globally more representative of human medulloblastoma compared to a MYCN-driven genetically engineered mouse model. Orthotopic transplantation of NES cells generated from Gorlin syndrome patients, who are predisposed to medulloblastoma due to germline-mutated PTCH1, also generated medulloblastoma. We engineered candidate cooperating mutations in Gorlin NES cells, with mutation of DDX3X or loss of GSE1 both accelerating tumorigenesis. These findings demonstrate that human NES cells provide a potent experimental resource for dissecting genetic causation in medulloblastoma.
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,
700 1 _ |a Tailor, Jignesh
|b 1
700 1 _ |a Zhen, Qiqi
|b 2
700 1 _ |a Gillmor, Aaron H
|b 3
700 1 _ |a Miller, Matthew L
|b 4
700 1 _ |a Weishaupt, Holger
|b 5
700 1 _ |a Chen, Justin
|b 6
700 1 _ |a Zheng, Tina
|b 7
700 1 _ |a Nash, Emily K
|b 8
700 1 _ |a McHenry, Lauren K
|b 9
700 1 _ |a An, Zhenyi
|b 10
700 1 _ |a Ye, Fubaiyang
|b 11
700 1 _ |a Takashima, Yasuhiro
|b 12
700 1 _ |a Clarke, James
|b 13
700 1 _ |a Ayetey, Harold
|b 14
700 1 _ |a Cavalli, Florence M G
|b 15
700 1 _ |a Luu, Betty
|b 16
700 1 _ |a Moriarity, Branden S
|b 17
700 1 _ |a Ilkhanizadeh, Shirin
|b 18
700 1 _ |a Chavez, Lukas
|0 P:(DE-He78)082dd3179733e3e716a58eb90f418a78
|b 19
|u dkfz
700 1 _ |a Yu, Chunying
|b 20
700 1 _ |a Kurian, Kathreena M
|b 21
700 1 _ |a Magnaldo, Thierry
|b 22
700 1 _ |a Sevenet, Nicolas
|b 23
700 1 _ |a Koch, Philipp
|0 P:(DE-HGF)0
|b 24
700 1 _ |a Pollard, Steven M
|b 25
700 1 _ |a Dirks, Peter
|b 26
700 1 _ |a Snyder, Michael P
|b 27
700 1 _ |a Largaespada, David A
|b 28
700 1 _ |a Cho, Yoon Jae
|b 29
700 1 _ |a Phillips, Joanna J
|b 30
700 1 _ |a Swartling, Fredrik J
|b 31
700 1 _ |a Morrissy, A Sorana
|b 32
700 1 _ |a Kool, Marcel
|0 P:(DE-He78)4c28e2aade5f44d8eca9dd8e97638ec8
|b 33
|u dkfz
700 1 _ |a Pfister, Stefan M
|0 P:(DE-He78)f746aa965c4e1af518b016de3aaff5d9
|b 34
|u dkfz
700 1 _ |a Taylor, Michael D
|b 35
700 1 _ |a Smith, Austin
|b 36
700 1 _ |a Weiss, William A
|b 37
773 _ _ |a 10.1016/j.stem.2019.05.013
|g p. S1934590919302176
|0 PERI:(DE-600)2375356-0
|n 3
|p 433-446.e7
|t Cell stem cell
|v 25
|y 2019
|x 1934-5909
909 C O |o oai:inrepo02.dkfz.de:144001
|p VDB
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 19
|6 P:(DE-He78)082dd3179733e3e716a58eb90f418a78
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 24
|6 P:(DE-HGF)0
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 33
|6 P:(DE-He78)4c28e2aade5f44d8eca9dd8e97638ec8
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 34
|6 P:(DE-He78)f746aa965c4e1af518b016de3aaff5d9
913 1 _ |a DE-HGF
|l Krebsforschung
|1 G:(DE-HGF)POF3-310
|0 G:(DE-HGF)POF3-312
|2 G:(DE-HGF)POF3-300
|v Functional and structural genomics
|x 0
|4 G:(DE-HGF)POF
|3 G:(DE-HGF)POF3
|b Gesundheit
914 1 _ |y 2019
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0300
|2 StatID
|b Medline
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0310
|2 StatID
|b NCBI Molecular Biology Database
915 _ _ |a JCR
|0 StatID:(DE-HGF)0100
|2 StatID
|b CELL STEM CELL : 2017
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0200
|2 StatID
|b SCOPUS
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0199
|2 StatID
|b Clarivate Analytics Master Journal List
915 _ _ |a WoS
|0 StatID:(DE-HGF)0110
|2 StatID
|b Science Citation Index
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0150
|2 StatID
|b Web of Science Core Collection
915 _ _ |a WoS
|0 StatID:(DE-HGF)0111
|2 StatID
|b Science Citation Index Expanded
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1030
|2 StatID
|b Current Contents - Life Sciences
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1050
|2 StatID
|b BIOSIS Previews
915 _ _ |a IF >= 20
|0 StatID:(DE-HGF)9920
|2 StatID
|b CELL STEM CELL : 2017
920 1 _ |0 I:(DE-He78)B062-20160331
|k B062
|l Pädiatrische Neuroonkologie
|x 0
980 _ _ |a journal
980 _ _ |a VDB
980 _ _ |a I:(DE-He78)B062-20160331
980 _ _ |a UNRESTRICTED


LibraryCollectionCLSMajorCLSMinorLanguageAuthor
Marc 21