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Start codon polymorphisms in the vitamin D receptor and colorectal cancer risk

The expression of the nuclear vitamin D receptor (VDR), which is involved in regulating cell growth and proliferation, may contribute to the development of colorectal cancer. Polymorphisms in the VDR gene (OMIM 601769) may influence the expression or function of the VDR protein. A population-based,...

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Published in:Cancer letters 2006-06, Vol.237 (2), p.199-206
Main Authors: Park, KyungSook, Woo, Mijung, Nam, JungHyun, Kim, Jin Cheon
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container_title Cancer letters
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creator Park, KyungSook
Woo, Mijung
Nam, JungHyun
Kim, Jin Cheon
description The expression of the nuclear vitamin D receptor (VDR), which is involved in regulating cell growth and proliferation, may contribute to the development of colorectal cancer. Polymorphisms in the VDR gene (OMIM 601769) may influence the expression or function of the VDR protein. A population-based, case-control study of VDR start codon, intron, and exon polymorphisms, haplotypes for these polymorphisms, and the relationships between these polymorphisms and clinicopathological parameters in 190 colorectal cancer patients and 318 controls was conducted. The start codon variant VDR 27823* C/* C genotype was associated with an increased risk for colorectal cancer, while the 27823* T/* T genotype was associated with a decreased risk. In addition, the VDR 61888* G/* G genotype was associated with reduced colorectal cancer risk. The intron 8 60880G>A and exon 9 61968T>C polymorphisms were not associated with colorectal cancer risk. The VDR 27823* C-60890* G-61888* T-61968* T haplotype was associated with an increased risk of colorectal cancer, whereas the VDR 27823* T-60890* G-61888* G-61968* T haplotype was associated with a decreased risk of colorectal cancer. Moreover, the 27823* C/* C genotype was more frequently identified in patients with preoperative serum carcinoembryonic antigen (CEA) levels over 6 ng/mL. These results suggest that the VDR start codon 27823* C allele may be linked to high risk for colorectal cancer, especially in a subset of colorectal cancers showing specific biological behaviors.
doi_str_mv 10.1016/j.canlet.2005.05.048
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These results suggest that the VDR start codon 27823* C allele may be linked to high risk for colorectal cancer, especially in a subset of colorectal cancers showing specific biological behaviors.</description><identifier>ISSN: 0304-3835</identifier><identifier>EISSN: 1872-7980</identifier><identifier>DOI: 10.1016/j.canlet.2005.05.048</identifier><identifier>PMID: 16019132</identifier><language>eng</language><publisher>Ireland: Elsevier Ireland Ltd</publisher><subject>Adult ; Age ; Aged ; Aged, 80 and over ; CEA ; Codon, Initiator ; Colon ; Colorectal cancer ; Colorectal Neoplasms - genetics ; Colorectal Neoplasms - pathology ; Confidence intervals ; Deoxyribonucleic acid ; DNA ; Enzymes ; Equilibrium ; Female ; Genes ; Genetic Predisposition to Disease ; Genotype ; Genotype &amp; phenotype ; Haplotypes ; Humans ; Male ; Middle Aged ; Patients ; Polymorphism ; Polymorphism, Genetic ; Proteins ; Receptors, Calcitriol - genetics ; Receptors, Calcitriol - metabolism ; Risk ; Rodents ; Vitamin D ; Vitamin D receptor</subject><ispartof>Cancer letters, 2006-06, Vol.237 (2), p.199-206</ispartof><rights>2005 Elsevier Ireland Ltd</rights><rights>Copyright Elsevier Limited Jun 18, 2006</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c454t-e056247abbae887c63ee4937434a2afde94d9df2d34472ddb47244b771ef77733</citedby><cites>FETCH-LOGICAL-c454t-e056247abbae887c63ee4937434a2afde94d9df2d34472ddb47244b771ef77733</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16019132$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Park, KyungSook</creatorcontrib><creatorcontrib>Woo, Mijung</creatorcontrib><creatorcontrib>Nam, JungHyun</creatorcontrib><creatorcontrib>Kim, Jin Cheon</creatorcontrib><title>Start codon polymorphisms in the vitamin D receptor and colorectal cancer risk</title><title>Cancer letters</title><addtitle>Cancer Lett</addtitle><description>The expression of the nuclear vitamin D receptor (VDR), which is involved in regulating cell growth and proliferation, may contribute to the development of colorectal cancer. Polymorphisms in the VDR gene (OMIM 601769) may influence the expression or function of the VDR protein. A population-based, case-control study of VDR start codon, intron, and exon polymorphisms, haplotypes for these polymorphisms, and the relationships between these polymorphisms and clinicopathological parameters in 190 colorectal cancer patients and 318 controls was conducted. The start codon variant VDR 27823* C/* C genotype was associated with an increased risk for colorectal cancer, while the 27823* T/* T genotype was associated with a decreased risk. In addition, the VDR 61888* G/* G genotype was associated with reduced colorectal cancer risk. The intron 8 60880G&gt;A and exon 9 61968T&gt;C polymorphisms were not associated with colorectal cancer risk. 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Polymorphisms in the VDR gene (OMIM 601769) may influence the expression or function of the VDR protein. A population-based, case-control study of VDR start codon, intron, and exon polymorphisms, haplotypes for these polymorphisms, and the relationships between these polymorphisms and clinicopathological parameters in 190 colorectal cancer patients and 318 controls was conducted. The start codon variant VDR 27823* C/* C genotype was associated with an increased risk for colorectal cancer, while the 27823* T/* T genotype was associated with a decreased risk. In addition, the VDR 61888* G/* G genotype was associated with reduced colorectal cancer risk. The intron 8 60880G&gt;A and exon 9 61968T&gt;C polymorphisms were not associated with colorectal cancer risk. 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subjects Adult
Age
Aged
Aged, 80 and over
CEA
Codon, Initiator
Colon
Colorectal cancer
Colorectal Neoplasms - genetics
Colorectal Neoplasms - pathology
Confidence intervals
Deoxyribonucleic acid
DNA
Enzymes
Equilibrium
Female
Genes
Genetic Predisposition to Disease
Genotype
Genotype & phenotype
Haplotypes
Humans
Male
Middle Aged
Patients
Polymorphism
Polymorphism, Genetic
Proteins
Receptors, Calcitriol - genetics
Receptors, Calcitriol - metabolism
Risk
Rodents
Vitamin D
Vitamin D receptor
title Start codon polymorphisms in the vitamin D receptor and colorectal cancer risk
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