001     169706
005     20240229133653.0
024 7 _ |a 10.1093/carcin/bgab057
|2 doi
024 7 _ |a pmid:34216462
|2 pmid
024 7 _ |a 0143-3334
|2 ISSN
024 7 _ |a 1460-2180
|2 ISSN
024 7 _ |a altmetric:108621205
|2 altmetric
037 _ _ |a DKFZ-2021-01513
041 _ _ |a English
082 _ _ |a 610
100 1 _ |a Pistoni, Laura
|b 0
245 _ _ |a Associations between pancreatic expression quantitative traits and risk of pancreatic ductal adenocarcinoma.
260 _ _ |a Oxford
|c 2021
|b Oxford Univ. Press
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 1642585094_1938
|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 Volume 42, Issue 8, August 2021, Pages 1037–1045
520 _ _ |a Pancreatic ductal adenocarcinoma (PDAC) is among the most lethal cancers. Its poor prognosis is predominantly due to the fact that most patients remain asymptomatic until the disease reaches an advanced stage, alongside the lack of early markers and screening strategies. A better understanding of PDAC risk factors is essential for the identification of groups at high risk in the population. Genome-wide association studies (GWAS) have been a powerful tool for detecting genetic variants associated with complex traits, including pancreatic cancer. By exploiting functional and GWAS data, we investigated the associations between polymorphisms affecting gene function in the pancreas (expression quantitative trait loci, eQTLs) and PDAC risk. In a two-phase approach, we analysed 13 713 PDAC cases and 43 784 controls and identified a genome-wide significant association between the A allele of the rs2035875 polymorphism and increased PDAC risk (P=7.14×10 -10). This allele is known to be associated with increased expression in the pancreas of the keratin genes KRT8 and KRT18, whose increased levels have been reported to correlate with various tumor cell characteristics. Additionally, the A allele of the rs789744 variant was associated with decreased risk of developing PDAC (P=3.56×10 -6). This SNP is situated in the SRGAP1 gene and the A allele is associated with higher expression of the gene, which in turn inactivates the cyclin-dependent protein 42 (CDC42) gene expression, thus decreasing the risk of PDAC. In conclusion, we present here a functional-based novel PDAC risk locus and an additional strong candidate supported by significant associations and plausible biological mechanisms.
536 _ _ |a 313 - Krebsrisikofaktoren und Prävention (POF4-313)
|0 G:(DE-HGF)POF4-313
|c POF4-313
|f POF IV
|x 0
588 _ _ |a Dataset connected to CrossRef, PubMed, , Journals: inrepo01.inet.dkfz-heidelberg.de
650 _ 7 |a association study
|2 Other
650 _ 7 |a eQTLs
|2 Other
650 _ 7 |a pancreatic cancer
|2 Other
650 _ 7 |a single nucleotide polymorphisms
|2 Other
700 1 _ |a Gentiluomo, Manuel
|b 1
700 1 _ |a Lu, Ye
|0 P:(DE-He78)ebb819874e9553d89bd480e6811dc0f3
|b 2
|u dkfz
700 1 _ |a López de Maturana, Evangelina
|b 3
700 1 _ |a Hlavac, Viktor
|b 4
700 1 _ |a Vanella, Giuseppe
|b 5
700 1 _ |a Darvasi, Erika
|b 6
700 1 _ |a Milanetto, Anna Caterina
|b 7
700 1 _ |a Oliverius, Martin
|b 8
700 1 _ |a Vashist, Yogesh
|b 9
700 1 _ |a Di Leo, Milena
|b 10
700 1 _ |a Mohelnikova-Duchonova, Beatrice
|b 11
700 1 _ |a Talar-Wojnarowska, Renata
|b 12
700 1 _ |a Gheorghe, Cristian
|b 13
700 1 _ |a Petrone, Maria Chiara
|b 14
700 1 _ |a Strobel, Oliver
|b 15
700 1 _ |a Arcidiacono, Paolo Giorgio
|b 16
700 1 _ |a Vodickova, Ludmila
|b 17
700 1 _ |a Szentesi, Andrea
|b 18
700 1 _ |a Capurso, Gabriele
|b 19
700 1 _ |a Gajdán, László
|b 20
700 1 _ |a Malleo, Giuseppe
|b 21
700 1 _ |a Theodoropoulos, George E
|b 22
700 1 _ |a Basso, Daniela
|b 23
700 1 _ |a Soucek, Pavel
|b 24
700 1 _ |a Brenner, Hermann
|0 P:(DE-He78)90d5535ff896e70eed81f4a4f6f22ae2
|b 25
|u dkfz
700 1 _ |a Lawlor, Rita T
|b 26
700 1 _ |a Morelli, Luca
|b 27
700 1 _ |a Ivanauskas, Audrius
|b 28
700 1 _ |a investigators, PanGenEU Study
|b 29
|e Collaboration Author
700 1 _ |a Kauffmann, Emanuele Federico
|b 30
700 1 _ |a Macauda, Angelica
|0 P:(DE-He78)b791a47b92809f7c54501331f72e0243
|b 31
|u dkfz
700 1 _ |a Gazouli, Maria
|0 0000-0002-3295-6811
|b 32
700 1 _ |a Archibugi, Livia
|b 33
700 1 _ |a Nentwich, Michael
|b 34
700 1 _ |a Loveček, Martin
|b 35
700 1 _ |a Cavestro, Giulia Martina
|b 36
700 1 _ |a Vodicka, Pavel
|b 37
700 1 _ |a Landi, Stefano
|b 38
700 1 _ |a Tavano, Francesca
|b 39
700 1 _ |a Sperti, Cosimo
|b 40
700 1 _ |a Hackert, Thilo
|0 0000-0002-7012-1196
|b 41
700 1 _ |a Kupcinskas, Juozas
|b 42
700 1 _ |a Pezzilli, Raffaele
|b 43
700 1 _ |a Andriulli, Angelo
|b 44
700 1 _ |a Pollina, Luca
|b 45
700 1 _ |a Kreivenaite, Edita
|b 46
700 1 _ |a Gioffreda, Domenica
|b 47
700 1 _ |a Jamroziak, Krzysztof
|b 48
700 1 _ |a Hegyi, Péter
|b 49
700 1 _ |a Izbicki, Jakob R
|b 50
700 1 _ |a Testoni, Sabrina Gloria Giulia
|b 51
700 1 _ |a Zuppardo, Raffaella Alessia
|b 52
700 1 _ |a Bozzato, Dania
|b 53
700 1 _ |a Neoptolemos, John P
|b 54
700 1 _ |a Malats, Núria
|b 55
700 1 _ |a Canzian, Federico
|0 P:(DE-He78)5323704270b6393dcea70186ffd86bca
|b 56
|u dkfz
700 1 _ |a Campa, Daniele
|b 57
773 _ _ |a 10.1093/carcin/bgab057
|g p. bgab057
|0 PERI:(DE-600)1474206-8
|n 8
|p 1037–1045
|t Carcinogenesis
|v 42
|y 2021
|x 1460-2180
909 C O |p VDB
|o oai:inrepo02.dkfz.de:169706
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 2
|6 P:(DE-He78)ebb819874e9553d89bd480e6811dc0f3
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 25
|6 P:(DE-He78)90d5535ff896e70eed81f4a4f6f22ae2
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 31
|6 P:(DE-He78)b791a47b92809f7c54501331f72e0243
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 56
|6 P:(DE-He78)5323704270b6393dcea70186ffd86bca
913 1 _ |a DE-HGF
|b Gesundheit
|l Krebsforschung
|1 G:(DE-HGF)POF4-310
|0 G:(DE-HGF)POF4-313
|3 G:(DE-HGF)POF4
|2 G:(DE-HGF)POF4-300
|4 G:(DE-HGF)POF
|v Krebsrisikofaktoren und Prävention
|x 0
913 0 _ |a DE-HGF
|b Gesundheit
|l Krebsforschung
|1 G:(DE-HGF)POF3-310
|0 G:(DE-HGF)POF3-313
|3 G:(DE-HGF)POF3
|2 G:(DE-HGF)POF3-300
|4 G:(DE-HGF)POF
|v Cancer risk factors and prevention
|x 0
914 1 _ |y 2021
915 _ _ |a Nationallizenz
|0 StatID:(DE-HGF)0420
|2 StatID
|d 2021-02-04
|w ger
915 _ _ |a JCR
|0 StatID:(DE-HGF)0100
|2 StatID
|b CARCINOGENESIS : 2019
|d 2021-02-04
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0200
|2 StatID
|b SCOPUS
|d 2021-02-04
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0300
|2 StatID
|b Medline
|d 2021-02-04
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0320
|2 StatID
|b PubMed Central
|d 2021-02-04
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0600
|2 StatID
|b Ebsco Academic Search
|d 2021-02-04
915 _ _ |a Peer Review
|0 StatID:(DE-HGF)0030
|2 StatID
|b ASC
|d 2021-02-04
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0199
|2 StatID
|b Clarivate Analytics Master Journal List
|d 2021-02-04
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1030
|2 StatID
|b Current Contents - Life Sciences
|d 2021-02-04
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0160
|2 StatID
|b Essential Science Indicators
|d 2021-02-04
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1050
|2 StatID
|b BIOSIS Previews
|d 2021-02-04
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1190
|2 StatID
|b Biological Abstracts
|d 2021-02-04
915 _ _ |a WoS
|0 StatID:(DE-HGF)0113
|2 StatID
|b Science Citation Index Expanded
|d 2021-02-04
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0150
|2 StatID
|b Web of Science Core Collection
|d 2021-02-04
915 _ _ |a IF < 5
|0 StatID:(DE-HGF)9900
|2 StatID
|d 2021-02-04
920 1 _ |0 I:(DE-He78)C055-20160331
|k C055
|l C055 Genomische Epidemiologie
|x 0
920 1 _ |0 I:(DE-He78)C070-20160331
|k C070
|l C070 Klinische Epidemiologie und Alternf.
|x 1
920 1 _ |0 I:(DE-He78)C120-20160331
|k C120
|l Präventive Onkologie
|x 2
920 1 _ |0 I:(DE-He78)HD01-20160331
|k HD01
|l DKTK HD zentral
|x 3
980 _ _ |a journal
980 _ _ |a VDB
980 _ _ |a I:(DE-He78)C055-20160331
980 _ _ |a I:(DE-He78)C070-20160331
980 _ _ |a I:(DE-He78)C120-20160331
980 _ _ |a I:(DE-He78)HD01-20160331
980 _ _ |a UNRESTRICTED


LibraryCollectionCLSMajorCLSMinorLanguageAuthor
Marc 21