Abstract

Trametes robiniophila Murr. (Huaier) is a mushroom with a long history of use as a medicinal ingredient in China and exhibits good clinical efficacy in cancer management. However, the antitumor components of Huaier and the underlying molecular mechanisms remain poorly understood. Here, we isolated a proteoglycan with a molecular mass of ∼5.59 × 104 Da from Huaier aqueous extract. We named this proteoglycan TPG-1, and using FTIR and additional biochemical analyses, we determined that its total carbohydrate and protein compositions are 43.9 and 41.2%, respectively. Using biochemical assays and immunoblotting, we found that exposing murine RAW264.7 macrophages to TPG-1 promotes the production of nitric oxide (NO), tumor necrosis factor α (TNFα), and interleukin-6 (IL-6) through Toll-like receptor 4 (TLR4)-dependent activation of NF-κB and mitogen-activated protein kinase (MAPK) signaling. Of note, the TPG-1 treatment significantly inhibited the tumorigenesis of human hepatoma HepG2 cells likely at least in part by increasing serum levels of TNFα and promoting leukocyte infiltration into tumors in nude mice. TPG-1 also exhibited good antitumor activity in hepatoma H22-bearing mice and had no obvious adverse effects in these mice. We conclude that TPG-1 exerts antitumor activity partially through an immune-potentiating effect due to activation of the TLR4-NF-κB/MAPK signaling cassette. Therefore, TPG-1 may be a promising candidate drug for cancer immunotherapy. This study has identified the TPG-1 proteoglycan as an antitumor agent and provided insights into TPG-1's molecular mechanism, suggesting a potential utility for applying this agent in cancer therapy.

Highlights

  • Trametes robiniophila Murr. (Huaier) is a mushroom with a long history of use as a medicinal ingredient in China and exhibits good clinical efficacy in cancer management

  • Using biochemical assays and immunoblotting, we found that exposing murine RAW264.7 macrophages to TPG-1 promotes the production of nitric oxide (NO), tumor necrosis factor ␣ (TNF␣), and interleukin-6 (IL-6) through Toll-like receptor 4 (TLR4)-dependent activation of NF-␬B and mitogen-activated protein kinase (MAPK) signaling

  • It has been reported that the immunomodulatory effect is one of underlying mechanisms of anti-tumor activity of Huaier [2, 7, 32]

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Summary

ARTICLE cro

An immune-stimulating proteoglycan from the medicinal mushroom Huaier up-regulates NF-␬B and MAPK signaling via Toll-like receptor 4. Using biochemical assays and immunoblotting, we found that exposing murine RAW264.7 macrophages to TPG-1 promotes the production of nitric oxide (NO), tumor necrosis factor ␣ (TNF␣), and interleukin-6 (IL-6) through Toll-like receptor 4 (TLR4)-dependent activation of NF-␬B and mitogen-activated protein kinase (MAPK) signaling. The TPG-1 treatment significantly inhibited the tumorigenesis of human hepatoma HepG2 cells likely at least in part by increasing serum levels of TNF␣ and promoting leukocyte infiltration into tumors in nude mice. The proteoglycan TPG-1 with a molecular mass of ϳ5.59 ϫ 104 Da was isolated from Huaier aqueous extract. Cancer immunotherapy of TPG-1 via TLR4 –NF-␬B/MAPK signaling necrosis factor ␣ (TNF␣), and interleukin-6 (IL-6) through TLR4-dependent activation of NF-␬B and MAPK signaling pathways in murine macrophage-like RAW264.7 cells. TPG-1 treatment significantly blunted the tumorigenic ability of HepG2 or H22 cells likely partially through facilitating the infiltration of leukocytes into tumors in mice

Results
Linkage type
Discussion
Reagents and antibodies
Cell culture
Glycosidic linkage analysis
Methylation analysis
The detection of molecular weight
Amino acid composition analysis
Microstructure observation
Cell viability assay
RNA sequence and data analysis
Determination of NO
IHC analysis
Statistical analysis
Full Text
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