Anti-tumor and immunomodulatory activities induced by an alkali-extracted polysaccharide BCAP-1 from Bupleurum chinense via NF-κB signaling pathway
•BCAP-1, an alkali-extracted polysaccharide from Bupleurum chinense, inhibited tumor growth in vivo and increased TNF-α in serum.•BCAP-1 treatment induced the phosphorylation of p65 and decreased the expression of IκB in peritoneal macrophages.•BCAP-1 activates macrophages through NF-κB signaling.•T...
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Veröffentlicht in: | International journal of biological macromolecules 2017-02, Vol.95, p.357-362 |
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Sprache: | eng |
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Zusammenfassung: | •BCAP-1, an alkali-extracted polysaccharide from Bupleurum chinense, inhibited tumor growth in vivo and increased TNF-α in serum.•BCAP-1 treatment induced the phosphorylation of p65 and decreased the expression of IκB in peritoneal macrophages.•BCAP-1 activates macrophages through NF-κB signaling.•The anti-tumor effects of BCAP-1 can be achieved by its immunostimulating property.
Bupleurum chinense is a well-known traditional Chinese medicine. Polysaccharides extracted from medical plants possess multiple healthy benefits. In the present study, an alkali-extracted polysaccharide (BCAP-1) was isolated from Bupleurum chinense, and evaluated its physicochemical features, anti-tumor activities and immunomodulatory effects. BCAP-1 was obtained by alkali-extraction, ethanol precipitation, and fractionation by DEAE-cellulose and Sepharose CL-6B columns. BCAP-1 markedly inhibited Sarcoma 180tumor growth in tumor-bearing mice, and increased the secretion of TNF-α in serum. MTT assay showed that BCAP-1 had no cytotoxicity against S-180 tumor cells. BCAP-1 enhanced the secretion of TNF-α and NO, and the transcripts of TNF-α and iNOS were increased. Meanwhile, BCAP-1 treatment induced the phosphorylation of p65 and decreased the expression of IκB in macrophages. These results suggest that BCAP-1 could activate macrophages through NF-κB signaling pathway, and the anti-tumor effects of BCAP-1 can be achieved by its immunostimulating features. |
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ISSN: | 0141-8130 1879-0003 |
DOI: | 10.1016/j.ijbiomac.2016.10.112 |