Antitumor and immunostimulatory activity of a polysaccharide–protein complex from Scolopendra subspinipes mutilans L. Koch in tumor-bearing mice

► A novel polysaccharide–protein complex from Scolopendra subspinipes mutilans (SPPC). ► SPPC suppressed the growth of sarcoma S180 and hepatoma H22 in vivo. ► SPPC remarkably enhanced antitumor immune responses in S180-bearing mice. ► SPPC inhibited arachidonic acid-metabolic pathways in tumor-asso...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Food and chemical toxicology 2012-08, Vol.50 (8), p.2648-2655
Hauptverfasser: Zhao, Haixia, Li, Ying, Wang, Yuzhong, Zhang, Jing, Ouyang, Xiaoming, Peng, Renxiu, Yang, Jing
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:► A novel polysaccharide–protein complex from Scolopendra subspinipes mutilans (SPPC). ► SPPC suppressed the growth of sarcoma S180 and hepatoma H22 in vivo. ► SPPC remarkably enhanced antitumor immune responses in S180-bearing mice. ► SPPC inhibited arachidonic acid-metabolic pathways in tumor-associated macrophages. ► SPPC could act as an anti-tumor agent with immunomodulatory activity. Scolopendra subspinipes mutilans L. Koch has been used for cancer treatment in traditional Chinese medicine for hundreds of years. In this study, the effects of a polysaccharide–protein complex from Scolopendra subspinipes mutilans L. Koch (SPPC) on the tumor growth and immune function were assessed in sarcoma S180 and hepatoma H22 bearing mice. Results showed that SPPC significantly inhibited the growth of S180 transplanted in mice and prolonged the survival time of H22- bearing mice. In S180-bearing mice, it promoted specific and nonspecific immune response as evidenced by enhancing the activities of natural killer (NK) cells, cytotoxic T lymphocytes (CTL) and the ratio of Th1/Th2 cytokines, and increasing the percentages of CD4+ T cells, B cells and NK cells. Furthermore, SPPC not only significantly inhibited mRNA expression and production of the immunosuppressive cytokines (IL-10 and TGF-β), but also diminished arachidonic acid (AA)-metabolizing enzymes (COX-2 and CYP4A) and their products (PGE2 and 20-HETE) in tumor-associated macrophages (TAMs). Taken together, our results indicate that SPPC inhibits tumor growth in vivo by improving antitumor immune responses at least partly via downregulating AA-metabolic pathways in TAMs, and could act as an anti-tumor agent with immunomodulatory activity.
ISSN:0278-6915
1873-6351
DOI:10.1016/j.fct.2012.05.018