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@ARTICLE{Corradi:291272,
author = {C. Corradi and G. Lencioni and A. Felici and C. Rizzato and
M. Gentiluomo and S. Ermini and L. Archibugi and A.
Mickevicius and M. Lucchesi and E. Malecka-Wojciesko and D.
Basso and P. G. Arcidiacono and M. C. Petrone and S. Carrara
and M. Götz and S. Bunduc and B. Holleczek and M. N. Aoki
and F. G. Uzunoglu and D. L. Zanette and A. Mambrini and K.
Jamroziak and M. Oliverius and M. Lovecek and G. M. Cavestro
and A. C. Milanetto and G. Peduzzi and B. M. Duchonova and
J. R. Izbicki and R. Zalinkevicius and V. Hlavac and C. H.
J. van Eijck and H. Brenner$^*$ and G. Vanella and K.
Vokacova and P. Soucek and F. Tavano and F. Perri and G.
Capurso and T. Hussein and M. Kiudelis and J. Kupcinskas and
O. R. Busch and L. Morelli and G. E. Theodoropoulos and S.
G. G. Testoni and K. Adamonis and J. P. Neoptolemos and M.
Gazouli and C. Pasquali and Z. Kormos and P. Skalicky and R.
Pezzilli and C. Sperti and E. Kauffmann and M. W. Büchler
and B. Schöttker$^*$ and P. Hegyi and G. Capretti and R. T.
Lawlor and F. Canzian$^*$ and D. Campa},
title = {{P}otential association between {PSCA} rs2976395 functional
variant and pancreatic cancer risk.},
journal = {International journal of cancer},
volume = {155},
number = {8},
issn = {0020-7136},
address = {Bognor Regis},
publisher = {Wiley-Liss},
reportid = {DKFZ-2024-01355},
pages = {1432-1442},
year = {2024},
note = {#LA:C055# / 2024 Oct 15;155(8):1432-1442},
abstract = {Correlated regions of systemic interindividual variation
(CoRSIV) represent a small proportion of the human genome
showing DNA methylation patterns that are the same in all
human tissues, are different among individuals, and are
partially regulated by genetic variants in cis. In this
study we aimed at investigating single-nucleotide
polymorphisms (SNPs) within CoRSIVs and their involvement
with pancreatic ductal adenocarcinoma (PDAC) risk. We
analyzed 29,099 CoRSIV-SNPs and 133,615 CoRSIV-mQTLs in
14,394 cases and 247,022 controls of European and Asian
descent. We observed that the A allele of the rs2976395 SNP
was associated with increased PDAC risk in Europeans (p =
2.81 × 10-5). This SNP lies in the prostate stem cell
antigen gene and is in perfect linkage disequilibrium with a
variant (rs2294008) that has been reported to be associated
with risk of many other cancer types. The A allele is
associated with the DNA methylation level of the gene
according to the PanCan-meQTL database and with
overexpression according to QTLbase. The expression of the
gene has been observed to be deregulated in many tumors of
the gastrointestinal tract including pancreatic cancer;
however, functional studies are needed to elucidate the
function relevance of the association.},
keywords = {DNA methylation (Other) / pancreatic cancer (Other) / risk
factors (Other) / single‐nucleotide polymorphism (Other)},
cin = {C070 / C120 / HD01 / C055},
ddc = {610},
cid = {I:(DE-He78)C070-20160331 / I:(DE-He78)C120-20160331 /
I:(DE-He78)HD01-20160331 / I:(DE-He78)C055-20160331},
pnm = {313 - Krebsrisikofaktoren und Prävention (POF4-313)},
pid = {G:(DE-HGF)POF4-313},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:38924078},
doi = {10.1002/ijc.35046},
url = {https://inrepo02.dkfz.de/record/291272},
}