A Survival Association Study of 102 Polymorphisms Previously Associated with Survival Outcomes in Colorectal Cancer

Several published studies identified associations of a number of polymorphisms with a variety of survival outcomes in colorectal cancer. In this study, we aimed to explore 102 previously reported common genetic polymorphisms and their associations with overall survival (OS) and disease-free survival...

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Published in:BioMed Research International
Main Authors: Savas, Sevtap, Xu, Jingxiong, Werdyani, Salem, Shestopaloff, Konstantin, Dicks, Elizabeth, Green, Jane, Parfrey, Patrick, Green, Roger, Xu, Wei
Format: Text
Language:English
Published: Hindawi Publishing Corporation 2015
Subjects:
Online Access:http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4443940/
https://doi.org/10.1155/2015/968743
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spelling ftpubmed:oai:pubmedcentral.nih.gov:4443940 2023-05-15T17:22:22+02:00 A Survival Association Study of 102 Polymorphisms Previously Associated with Survival Outcomes in Colorectal Cancer Savas, Sevtap Xu, Jingxiong Werdyani, Salem Shestopaloff, Konstantin Dicks, Elizabeth Green, Jane Parfrey, Patrick Green, Roger Xu, Wei 2015 http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4443940/ https://doi.org/10.1155/2015/968743 en eng Hindawi Publishing Corporation http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4443940/ http://dx.doi.org/10.1155/2015/968743 Copyright © 2015 Sevtap Savas et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. CC-BY Research Article Text 2015 ftpubmed https://doi.org/10.1155/2015/968743 2015-06-14T00:03:12Z Several published studies identified associations of a number of polymorphisms with a variety of survival outcomes in colorectal cancer. In this study, we aimed to explore 102 previously reported common genetic polymorphisms and their associations with overall survival (OS) and disease-free survival (DFS) in a colorectal cancer patient cohort from Newfoundland (n = 505). Genotypes were obtained using a genomewide SNP genotyping platform. For each polymorphism, the best possible genetic model was estimated for both overall survival and disease-free survival using a previously published approach. These SNPs were then analyzed under their genetic models by Cox regression method. Correction for multiple comparisons was performed by the False Discovery Rate (FDR) method. Univariate analysis results showed that RRM1-rs12806698, IFNGR1-rs1327474, DDX20-rs197412, and PTGS2-rs5275 polymorphisms were nominally associated with OS or DFS (p < 0.01). In stage-adjusted analysis, the nominal associations of DDX20-rs197412, PTGS2-rs5275, and HSPA5-rs391957 with DFS were detected. However, after FDR correction none of these polymorphisms remained significantly associated with the survival outcomes. We conclude that polymorphisms investigated in this study are not associated with OS or DFS in our colorectal cancer patient cohort. Text Newfoundland PubMed Central (PMC) BioMed Research International 2015 1 9
institution Open Polar
collection PubMed Central (PMC)
op_collection_id ftpubmed
language English
topic Research Article
spellingShingle Research Article
Savas, Sevtap
Xu, Jingxiong
Werdyani, Salem
Shestopaloff, Konstantin
Dicks, Elizabeth
Green, Jane
Parfrey, Patrick
Green, Roger
Xu, Wei
A Survival Association Study of 102 Polymorphisms Previously Associated with Survival Outcomes in Colorectal Cancer
topic_facet Research Article
description Several published studies identified associations of a number of polymorphisms with a variety of survival outcomes in colorectal cancer. In this study, we aimed to explore 102 previously reported common genetic polymorphisms and their associations with overall survival (OS) and disease-free survival (DFS) in a colorectal cancer patient cohort from Newfoundland (n = 505). Genotypes were obtained using a genomewide SNP genotyping platform. For each polymorphism, the best possible genetic model was estimated for both overall survival and disease-free survival using a previously published approach. These SNPs were then analyzed under their genetic models by Cox regression method. Correction for multiple comparisons was performed by the False Discovery Rate (FDR) method. Univariate analysis results showed that RRM1-rs12806698, IFNGR1-rs1327474, DDX20-rs197412, and PTGS2-rs5275 polymorphisms were nominally associated with OS or DFS (p < 0.01). In stage-adjusted analysis, the nominal associations of DDX20-rs197412, PTGS2-rs5275, and HSPA5-rs391957 with DFS were detected. However, after FDR correction none of these polymorphisms remained significantly associated with the survival outcomes. We conclude that polymorphisms investigated in this study are not associated with OS or DFS in our colorectal cancer patient cohort.
format Text
author Savas, Sevtap
Xu, Jingxiong
Werdyani, Salem
Shestopaloff, Konstantin
Dicks, Elizabeth
Green, Jane
Parfrey, Patrick
Green, Roger
Xu, Wei
author_facet Savas, Sevtap
Xu, Jingxiong
Werdyani, Salem
Shestopaloff, Konstantin
Dicks, Elizabeth
Green, Jane
Parfrey, Patrick
Green, Roger
Xu, Wei
author_sort Savas, Sevtap
title A Survival Association Study of 102 Polymorphisms Previously Associated with Survival Outcomes in Colorectal Cancer
title_short A Survival Association Study of 102 Polymorphisms Previously Associated with Survival Outcomes in Colorectal Cancer
title_full A Survival Association Study of 102 Polymorphisms Previously Associated with Survival Outcomes in Colorectal Cancer
title_fullStr A Survival Association Study of 102 Polymorphisms Previously Associated with Survival Outcomes in Colorectal Cancer
title_full_unstemmed A Survival Association Study of 102 Polymorphisms Previously Associated with Survival Outcomes in Colorectal Cancer
title_sort survival association study of 102 polymorphisms previously associated with survival outcomes in colorectal cancer
publisher Hindawi Publishing Corporation
publishDate 2015
url http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4443940/
https://doi.org/10.1155/2015/968743
genre Newfoundland
genre_facet Newfoundland
op_relation http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4443940/
http://dx.doi.org/10.1155/2015/968743
op_rights Copyright © 2015 Sevtap Savas et al.
This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
op_rightsnorm CC-BY
op_doi https://doi.org/10.1155/2015/968743
container_title BioMed Research International
container_volume 2015
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