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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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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | 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. |
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ISSN: | 0304-3835 1872-7980 |
DOI: | 10.1016/j.canlet.2005.05.048 |