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Physiol Int ; 107(1): 120-133, 2020 Mar.
Article de Anglais | MEDLINE | ID: mdl-32491284

RÉSUMÉ

BACKGROUND: Thyroid cancer is the most common endocrine malignancy. Studies have observed an anti-cancer effect for vitamin D and found that polymorphisms of vitamin D receptors can influence the prevalence of various cancers. The present study investigated the serum level of vitamin D and FokI, BsmI and Tru9I polymorphisms of vitamin D receptors. METHODS: Forty patients with medullary thyroid cancer and 40 healthy controls were investigated. The genomic DNA of the subjects was extracted using saturated salt/proteinase K and investigated by PCR sequencing. Serum levels of vitamin D were evaluated by ELISA. The results were analyzed in SPSS and GraphPad Prism 5 software. RESULTS: The genotypic and allelic frequencies of FokI and BsmI polymorphisms showed no significant differences between test and control groups. For Tru9I polymorphism, Tt genotype and t allelic frequency in the test group were significantly different from those of the control group. Also, we found Tt genotype and t allelic frequency to be significantly associated with medullary thyroid cancer (MTC) type and the agressiveness of the disease. The average serum vitamin D level was 23.32 ng/mL and 18.95 ng/mL for patients and controls, respectively, and the difference between the two groups was statistically significant. Moreover, we found high serum vitamin D level to be associated with t allelic frequency. CONCLUSIONS: Unexpectedly, the mean serum vitamin D level of the test group was significantly higher than that of the control group. Tru9I polymorphism was found to be significantly correlated with the prevalence of medullary thyroid carcinoma.


Sujet(s)
Carcinome neuroendocrine , Récepteur calcitriol/génétique , Tumeurs de la thyroïde , Vitamine D/sang , Adulte , Carcinome neuroendocrine/génétique , Carcinome neuroendocrine/métabolisme , Études cas-témoins , Corrélation de données , Femelle , Fréquence d'allèle , Prédisposition génétique à une maladie , Humains , Iran , Mâle , Polymorphisme de nucléotide simple , Tumeurs de la thyroïde/génétique , Tumeurs de la thyroïde/métabolisme
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