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Erschienen in: Comparative Clinical Pathology 1/2017

19.10.2016 | Original Article

Bsm1 Gene polymorphism of the vitamin D receptor in breast cancer patients: influence of obesity and relevant drugs

verfasst von: Noha Mohammed Ali Haikal, Mona Abo-Bakr El-Hussiny, Omar Farouk, Ekbal Mohammed Abo Hashem

Erschienen in: Comparative Clinical Pathology | Ausgabe 1/2017

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Abstract

Breast cancer (BC) is a common cancer among women, especially in developing countries. Circulating serum 25-hydroxyvitamin D [25(OH)D] is the key factor that regulates tissue synthesis of the active form 1,25-dihydroxyvitamin D [1,25(OH)2D]. 1,25(OH)2D has anticarcinogenic properties against breast cancer via binding to vitamin D receptors (VDRs). One of the common VDRs gene polymorphism which is located at the 3′ end of VDR gene is the Bsm-I gene polymorphism (rs1544410). Certain VDRs polymorphisms are associated with obesity and show relation to breast cancer risk. The current study was conducted on 60 breast cancer females and 30 healthy control subjects of matched age. Total serum 25(OH) vitamin D was measured using enzyme-linked immunosorbent assay (ELISA) technique. Vitamin D receptor VDR–Bsm1 gene polymorphism was assessed by PCR/RFLP method. Levels of 25(OH) vitamin D were significantly decreased in total, overweight, and obese BC patients in comparison to control group (p = 0.002, <0.001, <0.001, respectively). Regarding Bsm-1 polymorphism, no significant differences were observed between BC patients and control subjects with no risk to develop BC. Bsm-1 gene polymorphism is not associated with breast cancer risk and this result is not affected by increased BMI. A protective effect is observed for [25(OH)D] and ionized calcium levels against BC development.
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Metadaten
Titel
Bsm1 Gene polymorphism of the vitamin D receptor in breast cancer patients: influence of obesity and relevant drugs
verfasst von
Noha Mohammed Ali Haikal
Mona Abo-Bakr El-Hussiny
Omar Farouk
Ekbal Mohammed Abo Hashem
Publikationsdatum
19.10.2016
Verlag
Springer London
Erschienen in
Comparative Clinical Pathology / Ausgabe 1/2017
Print ISSN: 1618-5641
Elektronische ISSN: 1618-565X
DOI
https://doi.org/10.1007/s00580-016-2354-6

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