Enoki, Winter Mushroom · 2007 · Patent
Low relevanceAnti-tumor application of orally administrated FIP-fve on antitumor application
Flammulina velutipes
Key points
- The anti-tumor effect of FIP-fve, an immunomodulatory protein derived from Flammulina velutipes, was well demonstrated
- Oral administration of FIP-fve (200 mg protein/mouse) every other day significantly increased the survival of BNL 1MEA.7R.1 hepatoma-bearing mice and inhibits the growth of hepatoma (p < 0.05)
- In naive mice, orally administered FIP-fve enhanced the production of TNF-alpha and nitric oxide by peritoneal macrophages, whether in the presence or absence of LPS. In addition, peritoneal macrophages obtained from FIP-fve-fed naive mice had increased cytotoxicity against hepatoma cells (p < 0.05)
- In hepatoma-bearing mice, oral administration of FIP-fve significantly increased the serum levels of tumor-specific IgG (p < 0.05)
- Splenocytes obtained from FIP-fve-fed hepatoma-bearing mice had increased tumor-specific proliferation and upregulated production of IFN-gamma and TNF-alpha (p < 0.05), as well as enhanced cytotoxicity against hepatoma cells (p < 0.05)
From the paper
Abstract
The anti-tumor effect of FIP-fve, an immunomodulatory protein derived from Flammulina velutipes, was well demonstrated. Oral administration of FIP-fve (200 mg protein/mouse) every other day significantly increased the survival of BNL 1MEA.7R.1 hepatoma-bearing mice and inhibits the growth of hepatoma (p < 0.05). In naive mice, orally administered FIP-fve enhanced the production of TNF-alpha and nitric oxide by peritoneal macrophages, whether in the presence or absence of LPS. In addition, peritoneal macrophages obtained from FIP-fve-fed naive mice had increased cytotoxicity against hepatoma cells (p < 0.05). In hepatoma-bearing mice, oral administration of FIP-fve significantly increased the serum levels of tumor-specific IgG (p < 0.05). Splenocytes obtained from FIP-fve-fed hepatoma-bearing mice had increased tumor-specific proliferation and upregulated production of IFN-gamma and TNF-alpha (p < 0.05), as well as enhanced cytotoxicity against hepatoma cells (p < 0.05).
Citation
SHEU FUU, HSIEH KUANG-YANG, TU YUAN-PIN (2007). Anti-tumor application of orally administrated FIP-fve on antitumor application.
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