001     286670
005     20250731133736.0
024 7 _ |a 10.1002/ijc.34832
|2 doi
024 7 _ |a pmid:38175816
|2 pmid
024 7 _ |a 0020-7136
|2 ISSN
024 7 _ |a 1097-0215
|2 ISSN
024 7 _ |a altmetric:158171218
|2 altmetric
037 _ _ |a DKFZ-2024-00034
041 _ _ |a English
082 _ _ |a 610
100 1 _ |a Weijers, Dilys D
|0 0009-0004-0743-0756
|b 0
245 _ _ |a Molecular analysis of cancer genomes in children with Lynch syndrome: Exploring causal associations.
260 _ _ |a Bognor Regis
|c 2024
|b Wiley-Liss
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 1707979116_15286
|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
500 _ _ |a 2024 Apr 15;154(8):1455-1463
520 _ _ |a Lynch syndrome (LS) predisposes to cancer in adulthood and is caused by heterozygous germline variants in a mismatch repair (MMR) gene. Recent studies show an increased prevalence of LS among children with cancer, suggesting a causal relationship. For LS-spectrum (LSS) cancers, including high-grade gliomas and colorectal cancer, causality has been supported by typical MMR-related tumor characteristics, but for non-LSS cancers, causality is unclear. We characterized 20 malignant tumors of 18 children with LS, including 16 non-LSS tumors. We investigated second hits, tumor mutational load, mutational signatures and MMR protein expression. In all LSS tumors and three non-LSS tumors, we detected MMR deficiency caused by second hit somatic alterations. Furthermore, these MMR-deficient tumors carried driver variants that likely originated as a consequence of MMR deficiency. However, in 13 non-LSS tumors (81%), a second hit and MMR deficiency were absent, thus a causal link between LS and cancer development in these children is lacking. These findings demonstrate that causality of LS in children with cancer, which can be determined by molecular tumor characterization, seems to be restricted to specific tumor types. Large molecular and epidemiological studies are needed to further refine the tumor spectrum in children with LS.
536 _ _ |a 312 - Funktionelle und strukturelle Genomforschung (POF4-312)
|0 G:(DE-HGF)POF4-312
|c POF4-312
|f POF IV
|x 0
588 _ _ |a Dataset connected to CrossRef, PubMed, , Journals: inrepo02.dkfz.de
650 _ 7 |a Lynch syndrome
|2 Other
650 _ 7 |a cancer predisposition
|2 Other
650 _ 7 |a mismatch repair
|2 Other
650 _ 7 |a mutational signatures
|2 Other
650 _ 7 |a pediatric cancer
|2 Other
700 1 _ |a Hirsch, Steffen
|0 P:(DE-He78)5e3d4de4b59cd068969e101847794267
|b 1
|u dkfz
700 1 _ |a Bakhuizen, Jette J
|b 2
700 1 _ |a van Engelen, Nienke
|b 3
700 1 _ |a Kester, Lennart A
|b 4
700 1 _ |a Kranendonk, Mariëtte E G
|b 5
700 1 _ |a Hiemcke-Jiwa, Laura S
|b 6
700 1 _ |a de Vos-Kerkhof, Evelien
|b 7
700 1 _ |a Loeffen, Jan L C
|b 8
700 1 _ |a Autry, Robert
|0 P:(DE-He78)50c2928009c788a6a5f3a0708dfb6df5
|b 9
|u dkfz
700 1 _ |a Pajtler, Kristian
|0 P:(DE-He78)a7c1bbac024fa232d9c6b78443328d9d
|b 10
|u dkfz
700 1 _ |a Jäger, Natalie
|0 P:(DE-He78)bff9e3e3d86865d2b0836bb8f3ce98f3
|b 11
|u dkfz
700 1 _ |a Jongmans, Marjolijn C J
|b 12
700 1 _ |a Kuiper, Roland P
|b 13
773 _ _ |a 10.1002/ijc.34832
|g p. ijc.34832
|0 PERI:(DE-600)1474822-8
|n 8
|p 1455-1463
|t International journal of cancer
|v 154
|y 2024
|x 0020-7136
856 4 _ |u https://inrepo02.dkfz.de/record/286670/files/Intl%20Journal%20of%20Cancer%20-%202024%20-%20Weijers%20-%20Molecular%20analysis%20of%20cancer%20genomes%20in%20children%20with%20Lynch%20syndrome%20Exploring.pdf
856 4 _ |u https://inrepo02.dkfz.de/record/286670/files/Intl%20Journal%20of%20Cancer%20-%202024%20-%20Weijers%20-%20Molecular%20analysis%20of%20cancer%20genomes%20in%20children%20with%20Lynch%20syndrome%20Exploring.pdf?subformat=pdfa
|x pdfa
909 C O |p VDB
|o oai:inrepo02.dkfz.de:286670
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 1
|6 P:(DE-He78)5e3d4de4b59cd068969e101847794267
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 9
|6 P:(DE-He78)50c2928009c788a6a5f3a0708dfb6df5
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 10
|6 P:(DE-He78)a7c1bbac024fa232d9c6b78443328d9d
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 11
|6 P:(DE-He78)bff9e3e3d86865d2b0836bb8f3ce98f3
913 1 _ |a DE-HGF
|b Gesundheit
|l Krebsforschung
|1 G:(DE-HGF)POF4-310
|0 G:(DE-HGF)POF4-312
|3 G:(DE-HGF)POF4
|2 G:(DE-HGF)POF4-300
|4 G:(DE-HGF)POF
|v Funktionelle und strukturelle Genomforschung
|x 0
914 1 _ |y 2024
915 _ _ |a Nationallizenz
|0 StatID:(DE-HGF)0420
|2 StatID
|d 2023-10-21
|w ger
915 _ _ |a DEAL Wiley
|0 StatID:(DE-HGF)3001
|2 StatID
|d 2023-10-21
|w ger
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0200
|2 StatID
|b SCOPUS
|d 2023-10-21
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0300
|2 StatID
|b Medline
|d 2023-10-21
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0199
|2 StatID
|b Clarivate Analytics Master Journal List
|d 2023-10-21
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1050
|2 StatID
|b BIOSIS Previews
|d 2023-10-21
915 _ _ |a WoS
|0 StatID:(DE-HGF)0113
|2 StatID
|b Science Citation Index Expanded
|d 2023-10-21
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0150
|2 StatID
|b Web of Science Core Collection
|d 2023-10-21
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1030
|2 StatID
|b Current Contents - Life Sciences
|d 2023-10-21
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1190
|2 StatID
|b Biological Abstracts
|d 2023-10-21
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0160
|2 StatID
|b Essential Science Indicators
|d 2023-10-21
915 _ _ |a JCR
|0 StatID:(DE-HGF)0100
|2 StatID
|b INT J CANCER : 2022
|d 2023-10-21
915 _ _ |a IF >= 5
|0 StatID:(DE-HGF)9905
|2 StatID
|b INT J CANCER : 2022
|d 2023-10-21
920 1 _ |0 I:(DE-He78)B062-20160331
|k B062
|l B062 Pädiatrische Neuroonkologie
|x 0
920 1 _ |0 I:(DE-He78)HD01-20160331
|k HD01
|l DKTK HD zentral
|x 1
980 _ _ |a journal
980 _ _ |a VDB
980 _ _ |a I:(DE-He78)B062-20160331
980 _ _ |a I:(DE-He78)HD01-20160331
980 _ _ |a UNRESTRICTED


LibraryCollectionCLSMajorCLSMinorLanguageAuthor
Marc 21