| Literature DB >> 27253180 |
Keqiang Zhang1,2, Ernest S Han2, Thanh H Dellinger2, Jianming Lu1,2, Sangkil Nam1, Richard A Anderson3, John H Yim2, Wei Wen1,2.
Abstract
Although many anti-VEGF agents are available for cancer treatment, side effects of these agents limit their application for cancer treatment and prevention. Here we studied the potential use of a diet-based agent as an inhibitor for VEGF production. Using a VEGF reporter assay, our data showed that an extract from cinnamon (CE) was a potent inhibitor of VEGF production in human cancer cells and suggested inhibition might be mediated through the suppression of HIF-1α gene expression and protein synthesis. Furthermore, CE treatment was found to inhibit expression and phosphorylation of STAT3 and AKT, which are key factors in the regulation of HIF-1α expression, and significantly reduce angiogenesis potential of cancer cells by migration assay. Consistent with these results, we observed significant suppression of VEGF expression, blood vessel formation, and tumor growth in a human ovarian tumor model in mice treated with CE. Cinnamaldehyde, a major component in cinnamon, was identified as one active component in CE that inhibits VEGF expression. Taken together, our findings provide a novel mechanism underlying anti-angiogenic and anti-tumor actions of CE and support the potential use of CE in cancer prevention and treatment.Entities:
Keywords: HIF-1α; VEGF; angiogenesis; cinnamon extract; xenograft
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Year: 2016 PMID: 27253180 PMCID: PMC8830771 DOI: 10.1002/mc.22506
Source DB: PubMed Journal: Mol Carcinog ISSN: 0899-1987 Impact factor: 4.784