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Journal article

CD44 SNP rs187115: A novel biomarker signature that predicts survival in resectable pancreatic ductal adenocarcinoma.

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 single nucleotide polymorphisms (SNPs) in the CD44 gene, which drives the progression of pancreatic cancer.

Experimental Design

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 Projectdata 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.

Results

We identify a SNP in the CD44 gene (SNP rs187115) 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 rs187115. We validate those results in both the German (hazard ratio (HR)=2.32, p=0.044, 101 patients) and the TCGA cohort (HR=2.36, p=0.044, 126 patients).

Conclusions

CD44 SNP rs187115 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

Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1158/1078-0432.CCR-16-0058

Authors

More by this author
Institution:
University of Oxford
Division:
MSD
Department:
NDM
Sub department:
Oxford Ludwig Institute
Role:
Author


Publisher:
American Association for Cancer Research
Journal:
Clinical Cancer Research More from this journal
Volume:
22
Issue:
24
Pages:
6069-6077
Publication date:
2016-06-01
Acceptance date:
2016-05-19
DOI:
EISSN:
1078-0432
ISSN:
1078-0432


Language:
English
Keywords:
Pubs id:
pubs:628764
UUID:
uuid:e5ca38fe-12cb-4cdb-86a1-f3d5ee2968fd
Local pid:
pubs:628764
Source identifiers:
628764
Deposit date:
2016-06-22
ARK identifier:

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