Vitamin B6 Modifies the Immune Cross-Talk between Mononuclear and Colon Carcinoma Cells
Jazyk angličtina Země Česko Médium print
Typ dokumentu časopisecké články
PubMed
27085010
DOI
10.14712/fb2016062010047
PII: file/5802/fb2016a0006.pdf
Knihovny.cz E-zdroje
- MeSH
- antiflogistika metabolismus MeSH
- cytokiny metabolismus MeSH
- dospělí MeSH
- interferon gama metabolismus MeSH
- leukocyty mononukleární účinky léků imunologie MeSH
- lidé MeSH
- nádorové buněčné linie MeSH
- nádory tračníku imunologie patologie MeSH
- viabilita buněk účinky léků MeSH
- vitamin B6 farmakologie MeSH
- Check Tag
- dospělí MeSH
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- antiflogistika MeSH
- cytokiny MeSH
- interferon gama MeSH
- vitamin B6 MeSH
The role of vitamin B6 as a key component in a number of biological events has been well established. Based on the relationship between chronic inflammation and carcinogenesis on the one hand, and the interaction between immune and cancer cells expressed by modulated cytokine production on the other hand, the aim of the present work was to examine the possibility that vitamin B6 affects cancer development by an interference in the cross-talk between human peripheral blood mononuclear cells (PBMC) and those from two colon carcinoma cell lines. Both non-stimulated PBMC and mononuclear cells induced for cytokine production by HT-29 and RKO cells from human colon carcinoma lines were incubated without and with 4, 20 and 100 μg/ml of pyridoxal hydrochloride (vitamin B6) and secretion of TNF-α, IL-1β, IL-6, IFN-γ, IL-10, and IL-1ra was examined. Vit B6 caused a dose-dependent decrease in production of all cytokines examined, except for that of IL-1ra. The results indicate that vitamin B6 exerts an immunomodulatory effect on human PBMC. The finding that production of inflammatory cytokines is more pronounced when PBMC are in contact with malignant cells and markedly inhibited by the vitamin suggests an additional way by which vitamin B6 may exert its carcinopreventive effect.
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