<?xml version="1.0" encoding="UTF-8"?>
<records>
<record>
<language>eng</language>
<publisher>Science and Education Publishing</publisher>
<journalTitle>International Journal of Celiac Disease</journalTitle>
<eissn>2328-3955</eissn>
<publicationDate>2014-09-17</publicationDate>
<volume>2</volume>
<issue>3</issue>
<startPage>93</startPage>
<endPage>96</endPage>
<doi>10.12691/ijcd-2-3-6</doi>
<publisherRecordId>IJCD2014236</publisherRecordId>
<documentType>article</documentType>
<title language="eng">Genetic Aspects of Celiac Disease in Association with Pancreatic Tumors</title>
<authors>
<author>
<name>Pavel Procházka</name>
<email>proch.pavel@gmail.com</email>
<affiliationId>1</affiliationId>
</author>
</authors>
<affiliationsList>
<affiliationName affiliationId="1">Department of the Molecular Biology of Cancer, Institute of Experimental Medicine AS CR, Prague, Czech Republic</affiliationName>

</affiliationsList>
<abstract language="eng">Celiac disease stands out as a major health problem with a frequent association with many other disorders. Studies show an increased risk of developing pancreatitis and after that pancreatic cancer in patients with celiac disease. A frequent occurrence and a remarkably close association with the HLA-DQ2 and/or DQ8 gene loci represent main genetic characteristic of celiac disease. A particular association was found with chromosome 15q26 and 6q21-22. On the other hand pancreatic tumors are known for associations with CTNNB1, VHL, CDKN2A, KRAS, TP53, RNF43, SMAD4, GNAS, PRSS1, ATM, BRCA1, BRCA2, PALB2, STK11 and hereditary non-polyposis colorectal cancer syndrome genes. Recent genetic mapping suggests that a large field of opportunities exists for better understanding of both diseases.</abstract>
<fullTextUrl format="pdf">http://pubs.sciepub.com/ijcd/2/3/6/ijcd-2-3-6.pdf</fullTextUrl>
<keywords language="eng"><keyword>celiac disease</keyword>
<keyword>pancreatic tumors</keyword>
<keyword>HLA-DQ2 gene locus</keyword>
<keyword>DQ8 gene locus</keyword>
<keyword>KRAS</keyword>
<keyword>BRCA1/2</keyword>
</keywords>
</record>
</records>
