In vitro antiproliferative and antiangiogenic effects of Flavin7
Language English Country Czech Republic Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
18597584
DOI
10.33549/physiolres.931127
PII: 1127
Knihovny.cz E-resources
- MeSH
- Apoptosis drug effects MeSH
- Cell Cycle drug effects MeSH
- Endothelial Cells drug effects enzymology pathology MeSH
- Flavins pharmacology MeSH
- Flavonoids pharmacology MeSH
- DNA Fragmentation MeSH
- Antineoplastic Agents, Phytogenic pharmacology MeSH
- Neovascularization, Physiologic drug effects MeSH
- HeLa Cells MeSH
- Angiogenesis Inhibitors pharmacology MeSH
- Matrix Metalloproteinase Inhibitors MeSH
- Protease Inhibitors pharmacology MeSH
- Jurkat Cells MeSH
- Humans MeSH
- Cell Movement drug effects MeSH
- Dietary Supplements * MeSH
- Cell Proliferation drug effects MeSH
- Stilbenes pharmacology MeSH
- Cell Survival drug effects MeSH
- Dose-Response Relationship, Drug MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Flavin7 MeSH Browser
- Flavins MeSH
- Flavonoids MeSH
- Antineoplastic Agents, Phytogenic MeSH
- Angiogenesis Inhibitors MeSH
- Matrix Metalloproteinase Inhibitors MeSH
- Protease Inhibitors MeSH
- Stilbenes MeSH
Flavin7 (F7) is a nutritional supplement often taken by cancer patients in Central Europe during chemo- and radiation therapy. In this study, investigation of the antiproliferative and antiangiogenic activities of this supplement were performed. Flavin7 showed antiproliferative activity in Jurkat as well as in HeLa cells. It significantly reduced the growth of both cancer cell lines at the doses of 200 microg/ml to 20 microg/ml (p<0.001 and p<0.01, respectively). In F7-treated Jurkat cells we found a significant increase in the fraction of cells with sub-G(0)/G(1) DNA content, which is considered to be a marker of apoptotic cell death. Apoptosis was also confirmed by annexin V staining and DNA fragmentation. Furthermore, F7 at the doses of 100 microg/ml to 4 microg/ml inhibited endothelial cell migration and capillary tube formation what indicates its potential antiangiogenic properties. Flavin7 also inhibited the activity of matrix metalloproteinases (MMPs), preferentially MMP-9, at the doses of 100 microg/ml to 4 microg/ml. Our data suggest that F7 possesses marked antiproliferative and antiangiogenic properties in vitro. Further research is needed to elucidate also its in vivo activities.
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