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Vitamin D receptor polymorphisms and prostate cancer
D G Blazer1, D M Umbach, R M Bostick
1Laboratory of Molecular Carcinogenesis, NC, USA.
Molecular Carcinogenesis
|January 21, 2000
Summary
This study found no significant association between vitamin D receptor (VDR) gene polymorphisms (TaqI and poly(A)) and prostate cancer risk or advancement. Linkage disequilibrium was observed between these VDR polymorphisms.
Area of Science:
- Genetics
- Oncology
- Molecular Biology
Background:
- Prostate cancer risk factors are not fully understood, with low vitamin D levels implicated.
- Vitamin D receptor (VDR) gene polymorphisms, specifically TaqI and poly(A), have been previously linked to prostate cancer.
- VDR plays a role in the antineoplastic effects of 1,25-dihydroxy vitamin D (1,25-D).
Purpose of the Study:
- To investigate the association between VDR polymorphisms (TaqI and poly(A)) and prostate cancer risk.
- To examine if these VDR polymorphisms are associated with more advanced prostate cancer.
- To assess linkage disequilibrium between TaqI and poly(A) VDR polymorphisms.
Main Methods:
- A case-control study was conducted in North Carolina.
- DNA was extracted from peripheral blood of 77 prostate cancer cases and 183 controls.
- Polymerase chain reaction (PCR) techniques were used to genotype TaqI and poly(A) VDR alleles.
Main Results:
- No statistically significant association was found between TaqI or poly(A) VDR genotypes and prostate cancer risk (OR=1.4 and OR=1.2, respectively).
- No significant association was observed between these polymorphisms and advanced prostate cancer.
- Strong evidence of linkage disequilibrium between TaqI and poly(A) polymorphisms was detected (P < 0.0001), stronger in white participants.
Conclusions:
- The studied VDR polymorphisms (TaqI and poly(A)) do not appear to be significant risk factors for prostate cancer.
- These polymorphisms are not associated with disease progression in the studied population.
- Linkage disequilibrium exists between TaqI and poly(A) VDR polymorphisms, with ethnic variations noted.