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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 |
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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 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_68031423</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S030438350500546X</els_id><sourcerecordid>3241588781</sourcerecordid><originalsourceid>FETCH-LOGICAL-c454t-e056247abbae887c63ee4937434a2afde94d9df2d34472ddb47244b771ef77733</originalsourceid><addsrcrecordid>eNp9kMFq3DAQhkVJaLZJ3qAUQaA3byRrbNmXQkjatLAkhzZnIUtjoq1tuZJ2IW8fmV0o5BAYJCG-f2b4CPnM2ZozXl9v10ZPA6Z1yVi1XgqaD2TFG1kWsm3YCVkxwaAQjajOyKcYtyyDIKuP5IzXjLdclCvy8DvpkKjx1k909sPL6MP87OIYqZtoeka6d0mP-X1HAxqckw9UTzYnBp8_kh5o3sNgoMHFvxfktNdDxMvjfU6efnz_c_uz2Dze_7q92RQGKkgFsqouQequ09g00tQCEVohQYAudW-xBdvavrQCQJbWdvkE6KTk2EsphTgnXw995-D_7TAmNbpocBj0hH4XVd0wwaFcwKs34NbvwpR3U7xilZBCtixTcKBM8DEG7NUc3KjDi-JMLbbVVh1sq8W2WgqaHPtybL7rRrT_Q0e9Gfh2ADC72DsMKhqH2ZZ1iztlvXt_wivyq5HR</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1505373790</pqid></control><display><type>article</type><title>Start codon polymorphisms in the vitamin D receptor and colorectal cancer risk</title><source>ScienceDirect Freedom Collection 2022-2024</source><creator>Park, KyungSook ; Woo, Mijung ; Nam, JungHyun ; Kim, Jin Cheon</creator><creatorcontrib>Park, KyungSook ; Woo, Mijung ; Nam, JungHyun ; Kim, Jin Cheon</creatorcontrib><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.</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 & 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>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.</description><subject>Adult</subject><subject>Age</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>CEA</subject><subject>Codon, Initiator</subject><subject>Colon</subject><subject>Colorectal cancer</subject><subject>Colorectal Neoplasms - genetics</subject><subject>Colorectal Neoplasms - pathology</subject><subject>Confidence intervals</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>Enzymes</subject><subject>Equilibrium</subject><subject>Female</subject><subject>Genes</subject><subject>Genetic Predisposition to Disease</subject><subject>Genotype</subject><subject>Genotype & phenotype</subject><subject>Haplotypes</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Patients</subject><subject>Polymorphism</subject><subject>Polymorphism, Genetic</subject><subject>Proteins</subject><subject>Receptors, Calcitriol - genetics</subject><subject>Receptors, Calcitriol - metabolism</subject><subject>Risk</subject><subject>Rodents</subject><subject>Vitamin D</subject><subject>Vitamin D receptor</subject><issn>0304-3835</issn><issn>1872-7980</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNp9kMFq3DAQhkVJaLZJ3qAUQaA3byRrbNmXQkjatLAkhzZnIUtjoq1tuZJ2IW8fmV0o5BAYJCG-f2b4CPnM2ZozXl9v10ZPA6Z1yVi1XgqaD2TFG1kWsm3YCVkxwaAQjajOyKcYtyyDIKuP5IzXjLdclCvy8DvpkKjx1k909sPL6MP87OIYqZtoeka6d0mP-X1HAxqckw9UTzYnBp8_kh5o3sNgoMHFvxfktNdDxMvjfU6efnz_c_uz2Dze_7q92RQGKkgFsqouQequ09g00tQCEVohQYAudW-xBdvavrQCQJbWdvkE6KTk2EsphTgnXw995-D_7TAmNbpocBj0hH4XVd0wwaFcwKs34NbvwpR3U7xilZBCtixTcKBM8DEG7NUc3KjDi-JMLbbVVh1sq8W2WgqaHPtybL7rRrT_Q0e9Gfh2ADC72DsMKhqH2ZZ1iztlvXt_wivyq5HR</recordid><startdate>20060618</startdate><enddate>20060618</enddate><creator>Park, KyungSook</creator><creator>Woo, Mijung</creator><creator>Nam, JungHyun</creator><creator>Kim, Jin Cheon</creator><general>Elsevier Ireland Ltd</general><general>Elsevier Limited</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TO</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope></search><sort><creationdate>20060618</creationdate><title>Start codon polymorphisms in the vitamin D receptor and colorectal cancer risk</title><author>Park, KyungSook ; Woo, Mijung ; Nam, JungHyun ; Kim, Jin Cheon</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c454t-e056247abbae887c63ee4937434a2afde94d9df2d34472ddb47244b771ef77733</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Adult</topic><topic>Age</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>CEA</topic><topic>Codon, Initiator</topic><topic>Colon</topic><topic>Colorectal cancer</topic><topic>Colorectal Neoplasms - genetics</topic><topic>Colorectal Neoplasms - pathology</topic><topic>Confidence intervals</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>Enzymes</topic><topic>Equilibrium</topic><topic>Female</topic><topic>Genes</topic><topic>Genetic Predisposition to Disease</topic><topic>Genotype</topic><topic>Genotype & phenotype</topic><topic>Haplotypes</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Patients</topic><topic>Polymorphism</topic><topic>Polymorphism, Genetic</topic><topic>Proteins</topic><topic>Receptors, Calcitriol - genetics</topic><topic>Receptors, Calcitriol - metabolism</topic><topic>Risk</topic><topic>Rodents</topic><topic>Vitamin D</topic><topic>Vitamin D receptor</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Park, KyungSook</creatorcontrib><creatorcontrib>Woo, Mijung</creatorcontrib><creatorcontrib>Nam, JungHyun</creatorcontrib><creatorcontrib>Kim, Jin Cheon</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Cancer letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Park, KyungSook</au><au>Woo, Mijung</au><au>Nam, JungHyun</au><au>Kim, Jin Cheon</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Start codon polymorphisms in the vitamin D receptor and colorectal cancer risk</atitle><jtitle>Cancer letters</jtitle><addtitle>Cancer Lett</addtitle><date>2006-06-18</date><risdate>2006</risdate><volume>237</volume><issue>2</issue><spage>199</spage><epage>206</epage><pages>199-206</pages><issn>0304-3835</issn><eissn>1872-7980</eissn><abstract>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.</abstract><cop>Ireland</cop><pub>Elsevier Ireland Ltd</pub><pmid>16019132</pmid><doi>10.1016/j.canlet.2005.05.048</doi><tpages>8</tpages></addata></record> |
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issn | 0304-3835 1872-7980 |
language | eng |
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source | ScienceDirect Freedom Collection 2022-2024 |
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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