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pubmed-article:19768149pubmed:abstractTextRECQL is a DNA helicase involved in DNA mismatch repair. The RECQL polymorphism, 3' untranslated region (UTR) A159C, was previously associated with overall survival of patients with resectable pancreatic adenocarcinoma treated with neoadjuvant chemoradiation. In the present study, we examined RECQL for somatic mutations and other polymorphisms and compared these findings with the outcome in patients who received adjuvant or neoadjuvant chemoradiation. We hypothesized that RECQL (i) would be mutated in cancer, (ii) would have polymorphisms linked to the 3'UTR A159C and that either or both events would affect function. We also hypothesized that (iii) these changes would be associated with survival in both cohorts of patients.lld:pubmed
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pubmed-article:19768149pubmed:monthAuglld:pubmed
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pubmed-article:19768149pubmed:authorpubmed-author:LiDonghuiDlld:pubmed
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pubmed-article:19768149pubmed:volume11lld:pubmed
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pubmed-article:19768149pubmed:pagination435-44lld:pubmed
pubmed-article:19768149pubmed:dateRevised2010-8-3lld:pubmed
pubmed-article:19768149pubmed:year2009lld:pubmed
pubmed-article:19768149pubmed:articleTitleSingle nucleotide polymorphism in RECQL and survival in resectable pancreatic adenocarcinoma.lld:pubmed
pubmed-article:19768149pubmed:affiliationDepartment of Molecular and Human Genetics, Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX 77030, USA.lld:pubmed
pubmed-article:19768149pubmed:publicationTypeJournal Articlelld:pubmed
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