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Publication : Increased dietary vitamin D suppresses MAPK signaling, colitis, and colon cancer.

First Author  Meeker S Year  2014
Journal  Cancer Res Volume  74
Issue  16 Pages  4398-408
PubMed ID  24938764 Mgi Jnum  J:213720
Mgi Id  MGI:5585671 Doi  10.1158/0008-5472.CAN-13-2820
Citation  Meeker S, et al. (2014) Increased dietary vitamin D suppresses MAPK signaling, colitis, and colon cancer. Cancer Res 74(16):4398-408
abstractText  Epidemiologic studies associate low serum vitamin D levels with an increased risk of colon cancer and inflammatory diseases such as inflammatory bowel disease (IBD). 129-Smad3(tm1Par)/J (Smad3(-/-)) mice are a model of bacteria-driven colitis and colon cancer when infected with Helicobacter bilis (H. bilis). Thus, we used this mouse model to determine whether increased dietary vitamin D would reduce inflammation and colon cancer. Smad3(-/-) mice were fed purified diet with either maintenance (1 IU vitamin D/g diet; maintenance) or increased concentrations of vitamin D (5 IU vitamin D/g diet; high vitamin D). One week after diet initiation, mice were inoculated with broth or H. bilis and were necropsied at several time points postinoculation to assess inflammation, dysplasia, and neoplasia incidence. At 16 weeks postinfection, 11% of mice fed high vitamin D diet had cancer compared with 41% of mice fed maintenance diet (P = 0.0121). Evaluation at an early time point (1 week postinfection) showed that animals fed high vitamin D had decreased MAPK (p-P38 and p-JNK) activation in lamina propria leukocytes as well as decreased NFkappaB activation in colonic epithelial cells. Reduction in MAPK and NFkappaB activation correlated with decreased IBD scores (2.7 vs. 15.5; P < 0.0001) as well as decreased inflammatory cell infiltrates and reduced expression of proinflammatory cytokines in cecal tissue. These findings suggest that increased dietary vitamin D is beneficial in preventing inflammation-associated colon cancer through suppression of inflammatory responses during initiation of neoplasia or early-stage carcinogenesis.
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