Fucoidan from Sargassum sp and Fucus vesiculosus reduces cell viability of lung carcinoma and melanoma cells in vitro and activates natural killer cells in mice in vivo

被引:206
作者
Ale, Marcel Tutor [1 ]
Maruyama, Hiroko [2 ]
Tamauchi, Hidekazu [3 ]
Mikkelsen, Jorn D. [1 ]
Meyer, Anne S. [1 ]
机构
[1] Tech Univ Denmark DTU, Ctr Bioproc Engn, Dept Chem & Biochem Engn, DK-2800 Lyngby, Denmark
[2] Kitasato Univ, Dept Pathol, Sch Allied Sci, Kanagawa 2288555, Japan
[3] Kitasato Univ, Dept Microbiol, Sch Med, Kanagawa 2288555, Japan
关键词
Fucoidan; Seaweed; Apoptosis; Immune-response; Anti-tumor; ANTITUMOR-ACTIVITY; APOPTOSIS; CANCER; ANTICOAGULANT; LAMINARIA; SEAWEEDS; DISEASE; MEKABU;
D O I
10.1016/j.ijbiomac.2011.05.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Fucoidan is known to exhibit crucial biological activities, including anti-tumor activity. In this study, we examined the influence of crude fucoidan extracted from Sargassum sp. (MTA) and Fucus vesiculosus (SIG) on Lewis lung carcinoma cells (LCC) and melanoma B16 cells (MC). In vitro studies were performed using cell viability analysis and showed that SIG and MTA fucoidans significantly decreased the viable number of LCC and MC cells in a dose-response fashion. Histochemical staining showed morphological changes of melanoma B16 cells after exposure to fucoidan. The observed changes were indicative of crude fucoidan induced apoptosis. Male C57BL/6JJCL mice were subjected to daily i.p. injections over 4 days with either SIG or MTA fucoidan (50 mg/kg body wt.). The cytolytic activity of natural killer (NK) cells was enhanced by crude fucoidan in a dose-dependent manner as indicated by (51)Cr labeled YAC-1 target cell release. This study provides substantial indications that crude fucoidan exerts bioactive effects on lung and skin cancer model cells in vitro and induces enhanced natural killer cell activity in mice in vivo. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:331 / 336
页数:6
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