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Vitamin D Pathway Genes, Diet, and Risk of Renal Cell Carcinoma
- Source :
- International Journal of Endocrinology, Vol 2010 (2010), International Journal of Endocrinology
- Publication Year :
- 2010
- Publisher :
- Hindawi Limited, 2010.
-
Abstract
- Mediated by binding to the high-affinity vitamin D receptor (VDR), vitamin D forms a heterodimer complex with the retinoid-X-receptor (RXR). Variation in both genes has been shown to modify renal cell carcinoma (RCC) risk. Therefore, we investigated whetherVDRandRXRApolymorphisms modify associations between RCC risk and frequency of dietary intake of vitamin D and calcium rich foods, and occupational ultraviolet exposure among 777 RCC case and 1035 controls from Central and Eastern Europe. A positive association was observed in this population between increasing dietary intake frequency of yogurt, while an inverse association was observed with egg intake frequency.RXRApolymorphisms, located3′of the coding sequence, modified associations between specific vitamin D rich foods and RCC risk, whileRXRApolymorphisms, located in introns 1 and 4, modified associations with specific calcium rich foods. Results suggest that variants in theRXRAgene modified the associations observed between RCC risk and calcium and vitamin D intake.
- Subjects :
- medicine.medical_specialty
renal cell carcinoma
Article Subject
Endocrinology, Diabetes and Metabolism
Population
chemistry.chemical_element
Retinoid X receptor
Calcium
urologic and male genital diseases
Calcitriol receptor
lcsh:Diseases of the endocrine glands. Clinical endocrinology
Endocrinology
Renal cell carcinoma
Internal medicine
medicine
Vitamin D and neurology
education
Gene
education.field_of_study
lcsh:RC648-665
Endocrine and Autonomic Systems
business.industry
Intron
medicine.disease
chemistry
Vitamin d
business
diet
Research Article
Subjects
Details
- Language :
- English
- ISSN :
- 16878345 and 16878337
- Volume :
- 2010
- Database :
- OpenAIRE
- Journal :
- International Journal of Endocrinology
- Accession number :
- edsair.doi.dedup.....2e4edcd67ae5eb8c083669f776062047