Liver cancer incidence probably reduced by Vitamin D and Vitamin K
Vitamin D and K signaling pathways in hepatocellular carcinoma
Gene, Available online 29 July 2017, https://doi.org/10.1016/j.gene.2017.07.074
Manal L. Loukaa, Ahmed M. Fawzyb, Abdelrahman M. Naiemb, Mustafa F. Elseknedyb, Ahmed E. Abdelhalimb, Mohamed A. Abdelghanyb
Highlights
• Early diagnosis of HCC with prompt treatment increases the opportunity of patients to survive.
• Vitamins are important for the control of various cancers.
• Vitamin D and K influence the development of HCC.
• The active form of vitamin D and vitamin K exert an array of antitumor activities.
• Vitamin analogues have a potential role in HCC therapy.
Hepatocellular carcinoma (HCC) is a primary liver malignancy, and is now the six most common in between malignancies. Early diagnosis of HCC with prompt treatment increases the opportunity of patients to survive. With the advances in understanding the molecular biology of HCC, new therapeutic strategies to treat HCC have emerged. There is a growing consensus that vitamins are important for the control of various cancers. Biochemical evidence clearly indicates that HCC cells are responsive to the inhibitory effect of vitamin D, vitamin D analogues and vitamin K. In this review, we summarize the mechanisms used by vitamin D and K to influence the development of HCC and the latest development of vitamin analogues for potential HCC therapy.
Abbreviations
(1,25(OH)2D3), 1,25-dihydroxycholecalciferol; (7-DHC), 7-dehydrocholesterol; (BCLC), Barcelona-Clınic Liver Cancer; (EPIC), The European Prospective Investigation into Cancer and Nutrition; (GGCX), gamma-glutamyl carboxylase; (HCC), hepatocellular carcinoma; (HDAC2), histone deacetylase 2; (HIF)-1, hypoxia inducible factor; (MMP-9), matrix metalloproteinase 9; (MAPK), mitogen-activated protein kinase; (PCT), proximal convoluted tubule; (PEGIFN), pegylated interferone; (PKC), protein kinase C; (RBV), ribavirin; (SNPs), single nucleotide polymorphisms; (SVR), sustained virological response; (TXNIP), thioredoxin-interacting protein; (TACE), trans-arterial chemo-embolisation; (TGF-β), transforming growth factor B; (VEGF), vascular endothelial growth factor; (DBP), vitamin D binding protein; (VDR), vitamin D receptor