Meta-analysis of vitamin D-binding protein and cancer risk.
Cancer Epidemiol Biomarkers Prev. 2015 Sep 12. pii: cebp.0262.2015. [Epub ahead of print]
Tagliabue E1, Raimondi S2, Gandini S3.
BACKGROUND:
Epidemiologic evidence supported a role for vitamin D and vitamin D receptor (VDR) polymorphisms in cancer risk. Beyond VDR, the biological effects of vitamin D are mediated by the vitamin D binding protein (DBP), a key protein in vitamin D metabolism. Furthermore, the gene encoding the DBP (GC, Group-specific component) has an important role in vitamin D pathway. Several studies investigated DBP serological levels and GC polymorphisms in association with cancer risk with controversial results. Thus we carried out a meta-analysis to investigate these associations.
METHODS:
We included 28 independent studies concerning: basal cell carcinoma, bladder, breast, colon-rectum, endometrium, liver, esophagus, stomach, melanoma, pancreas, prostate and kidney. Through random effect models we calculated the Summary Odd Ratios (SORs) for serum DBP and the GC polymorphisms rs2282679, rs12512631, rs7041, rs4588, rs17467825, rs1155563 and rs1352844.
RESULTS:
We found a borderline decrease in cancer risk for subjects with high compared to low levels of DBP (SOR;95%CI:0.75;0.56-1.00). Dose-response meta-analysis indicate a non-significant decrease risk for an increase of 1,000 nmol/L of DBP: (SOR;95%CI:0.96;0.91-1.01). We found no significant alterations in cancer risk for subjects carrying any of the studied GC polymorphisms compared to wild-type subjects both in the main analysis and in analyses stratified by cancer type and ethnicity.
CONCLUSIONS:
We found trends toward significance suggesting a role of DBP in cancer etiology, that should be confirmed in further studies.
IMPACT:
To our knowledge, this is the first study to investigate GC polymorphisms and DBP serological levels in association with any type of cancer.
Copyright © 2015, American Association for Cancer Research.
PMID: 26364161
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