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CD44 SNPrs187115: A Novel Biomarker Signature that Predicts Survival in Resectable Pancreatic Ductal Adenocarcinoma.
- Source :
-
Clinical cancer research : an official journal of the American Association for Cancer Research [Clin Cancer Res] 2016 Dec 15; Vol. 22 (24), pp. 6069-6077. Date of Electronic Publication: 2016 Jun 09. - Publication Year :
- 2016
-
Abstract
- Purpose: Although pancreatic ductal adenocarcinoma (PDAC) is an aggressive tumor, like other common cancers, it displays a wide range of biology. However, at present, there are no reliable tests to predict patients' cancer-specific outcomes and guide personalized treatment decisions. In this study, we aim to identify such biomarkers in resectable PDAC by studying SNPs in the CD44 gene, which drives the progression of pancreatic cancer.<br />Experimental Design: A total of 348 PDAC patients from three independent cohorts [Switzerland, Germany, The Cancer Genome Atlas (TCGA)] who underwent pancreatic resection are included in the study. Information on the haplotype structure of the CD44 gene is obtained using 1000 Genomes Project data, and the genotypes of the respective tagging SNPs are determined. Cox proportional hazards models are utilized to analyze the impact of SNP genotype on patients' survival.<br />Results: We identify an SNP in the CD44 gene (SNP <superscript>rs187115</superscript> ) that independently associates with allelic differences in prognosis in all study cohorts. Specifically, in 121 Swiss patients, we observe an up to 2.38-fold (P = 0.020) difference in tumor-related death between the genotypes of SNP <superscript>rs187115</superscript> We validate those results in both the German (HR = 2.32, P = 0.044, 101 patients) and the TCGA cohort (HR = 2.36, P = 0.044, 126 patients).<br />Conclusions: CD44 SNP <superscript>rs187115</superscript> can serve as a novel biomarker readily available at the time of PDAC diagnosis that identifies patients at risk for faster tumor progression and guide personalized treatment decisions. It has the potential to significantly expand the pool of patients that would benefit from tumor resection. Clin Cancer Res; 22(24); 6069-77. ©2016 AACR.<br /> (©2016 American Association for Cancer Research.)
- Subjects :
- Adenocarcinoma pathology
Adult
Aged
Aged, 80 and over
Carcinoma, Pancreatic Ductal pathology
Cohort Studies
Disease Progression
Female
Gene Expression Regulation, Neoplastic genetics
Humans
Male
Middle Aged
Pancreatic Neoplasms pathology
Prognosis
Proportional Hazards Models
Young Adult
Adenocarcinoma genetics
Biomarkers, Tumor genetics
Carcinoma, Pancreatic Ductal genetics
Hyaluronan Receptors genetics
Pancreatic Neoplasms genetics
Polymorphism, Single Nucleotide genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1557-3265
- Volume :
- 22
- Issue :
- 24
- Database :
- MEDLINE
- Journal :
- Clinical cancer research : an official journal of the American Association for Cancer Research
- Publication Type :
- Academic Journal
- Accession number :
- 27283965
- Full Text :
- https://doi.org/10.1158/1078-0432.CCR-16-0058