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@ARTICLE{Yuan:157047,
      author       = {F. Yuan and R. J. Hung and N. Walsh and H. Zhang and E. A.
                      Platz and W. Wheeler and L. Song and A. A. Arslan and L. E.
                      Beane Freeman and P. Bracci and F. Canzian$^*$ and M. Du and
                      S. Gallinger and G. G. Giles and P. J. Goodman and C.
                      Kooperberg and L. Le Marchand and R. E. Neale and J.
                      Rosendahl and G. Scelo and X.-O. Shu and K. Visvanathan and
                      E. White and W. Zheng and D. Albanes and P. Amiano and G.
                      Andreotti and A. Babic and W. R. Bamlet and S. I. Berndt and
                      P. Brennan and B. Bueno-de-Mesquita and J. E. Buring and P.
                      T. Campbell and S. J. Chanock and C. S. Fuchs and J. M.
                      Gaziano and M. G. Goggins and T. Hackert and P. Hartge and
                      M. M. Hassan and E. A. Holly and R. N. Hoover and V.
                      Katzke$^*$ and H. Kirsten and R. C. Kurtz and I.-M. Lee and
                      N. Malats and R. Milne and N. Murphy and K. Ng and A. L.
                      Oberg and M. Porta and K. G. Rabe and F. X. Real and N.
                      Rothman and H. D. Sesso and D. T. Silverman and I. M.
                      Thompson and J. Wactawski-Wende and X. Wang and N.
                      Wentzensen and L. R. Wilkens and H. Yu and A.
                      Zeleniuch-Jacquotte and J. Shi and E. J. Duell and L. T.
                      Amundadottir and D. Li and G. M. Petersen and B. M. Wolpin
                      and H. A. Risch and K. Yu and A. P. Klein and R.
                      Stolzenberg-Solomon},
      title        = {{G}enome-wide association study data reveal genetic
                      susceptibility to chronic inflammatory intestinal diseases
                      and pancreatic ductal adenocarcinoma risk.},
      journal      = {Cancer research},
      volume       = {80},
      number       = {18},
      issn         = {1538-7445},
      address      = {Philadelphia, Pa.},
      publisher    = {AACR},
      reportid     = {DKFZ-2020-01338},
      pages        = {4004-4013},
      year         = {2020},
      note         = {2020 Sep 15;80(18):4004-4013},
      abstract     = {Registry-based epidemiologic studies suggest associations
                      between chronic inflammatory intestinal diseases and
                      pancreatic ductal adenocarcinoma (PDAC). As genetic
                      susceptibility contributes to a large proportion of chronic
                      inflammatory intestinal diseases, we hypothesize that the
                      genomic regions surrounding established genome-wide
                      associated variants for these chronic inflammatory diseases
                      are associated with PDAC. We examined the association
                      between PDAC and genomic regions (+/- 500 kb) surrounding
                      established common susceptibility variants for ulcerative
                      colitis, Crohn's disease, inflammatory bowel disease, celiac
                      disease, chronic pancreatitis, and primary sclerosing
                      cholangitis. We analyzed summary statistics from genome-wide
                      association studies data for 8,384 cases and 11,955 controls
                      of European descent from two large consortium studies using
                      the summary data-based adaptive rank truncated product
                      method to examine the overall association of combined
                      genomic regions for each inflammatory disease group.
                      Combined genomic susceptibility regions for ulcerative
                      colitis, Crohn's disease, inflammatory bowel disease, and
                      chronic pancreatitis were associated with PDAC at P-values <
                      0.05 (0.0040, 0.0057, 0.011, and 3.4 × 10-6, respectively).
                      After excluding the 20 PDAC susceptibility regions (+/- 500
                      kb) previously identified by GWAS, the genomic regions for
                      ulcerative colitis, Crohn's disease, and inflammatory bowel
                      disease remained associated with PDAC (P-values = 0.0029,
                      0.0057, and 0.0098, respectively). Genomic regions for
                      celiac disease (P-value = 0.22) and primary sclerosing
                      cholangitis (P-value = 0.078) were not associated with PDAC.
                      Our results support the hypothesis that genomic regions
                      surrounding variants associated with inflammatory intestinal
                      diseases, particularly, ulcerative colitis, Crohn's disease,
                      inflammatory bowel disease, and chronic pancreatitis are
                      associated with PDAC.},
      cin          = {C055 / C020},
      ddc          = {610},
      cid          = {I:(DE-He78)C055-20160331 / I:(DE-He78)C020-20160331},
      pnm          = {313 - Cancer risk factors and prevention (POF3-313)},
      pid          = {G:(DE-HGF)POF3-313},
      typ          = {PUB:(DE-HGF)16},
      pubmed       = {pmid:32641412},
      doi          = {10.1158/0008-5472.CAN-20-0447},
      url          = {https://inrepo02.dkfz.de/record/157047},
}