Effects of the antlered form of Ganoderma lucidum on tumor growth and metastasis in cyclophosphamide-treated mice

被引:27
作者
Nonaka, Yuji [1 ]
Ishibashi, Hiroko [2 ]
Nakai, Masaaki [1 ]
Shibata, Hiroshi [1 ]
Kiso, Yoshinobu [1 ]
Abe, Shigeru [2 ]
机构
[1] Suntory Ltd, Inst Hlth Care Sci, Shimamoto, Osaka 6188503, Japan
[2] Teikyo Univ, Inst Med Mycol, Tokyo 1920395, Japan
关键词
antlered form of Ganoderma lucidum; cyclophosphamide; anti-tumor activity; anti-metastatic activity; immunodepression;
D O I
10.1271/bbb.70607
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
We examined the alleviation of cyclophosphamide-induced immunodepression by the antlered form of Ganoderma lucidum (G. lucidum AF) and also evaluated the anti-tumor and anti-metastatic effects of G. lucidum AF in cyclophosphamide-treated mice. G. lucidum AF alleviated cyclophosphamide-induced decrease in body weight, natural killer (NK) activity, interferon (IFN)-gamma production, and cytotoxic T lymphocyte (CTL) activity, and inhibited the abnormal increase and decrease in interleukine (IL)-4 level due to cyclophosphamide administration. Post-treatment with cyclophosphamide and G. lucidum AF significantly inhibited tumor growth in MM 46-bearing mice. When Lewis lung carcinoma cells were injected into mice after a cyclophosphamide administration, metastasis of these cells to the lung was increased, but G. lucidum AF suppressed it. The antitumor and anti-metastatic effects of the combination of G. lucidum AF and cyclophosphamide might influence the modulatory effects of G. lucidum AF on both cellular and humoral immunity. These findings suggest that G. lucidum AF would be beneficial in alleviating the reduction of immune response by chemotherapeutic anti-cancer drugs.
引用
收藏
页码:1399 / 1408
页数:10
相关论文
共 33 条
[1]
Immunosuppressive drugs, the first 50 years and a glance forward [J].
Allison, AC .
IMMUNOPHARMACOLOGY, 2000, 47 (2-3) :63-83
[2]
Dectin-1 mediates the biological effects of β-glucans [J].
Brown, GD ;
Herre, J ;
Williams, DL ;
Willment, JA ;
Marshall, ASJ ;
Gordon, S .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 197 (09) :1119-1124
[3]
Chapoval AI, 1998, J IMMUNOL, V161, P6977
[4]
CZOP JK, 1985, J IMMUNOL, V135, P3388
[5]
Antitumour effect of OM-174 and Cyclophosphamide on murine B16 melanoma in different experimental conditions [J].
D'Agostini, C ;
Pica, F ;
Febbraro, G ;
Grelli, S ;
Chiavaroli, C ;
Garaci, E .
INTERNATIONAL IMMUNOPHARMACOLOGY, 2005, 5 (7-8) :1205-1212
[6]
Goldfarb RH, 1998, ANTICANCER RES, V18, P1441
[7]
Cancer cell progression and chemoimmunotherapy - Dual effects in the induction of resistance to therapy [J].
Hamuro, J ;
Kikuchi, T ;
Takatsuki, F ;
Suzuki, M .
BRITISH JOURNAL OF CANCER, 1996, 73 (04) :465-471
[8]
Effect of SCG, 1,3-β-D-glucan from Sparassis crispa on the hematopoietic response in cyclophosphamide induced leukopenic mice [J].
Harada, T ;
Miura, N ;
Adachi, Y ;
Nakajima, M ;
Yadomae, T ;
Ohno, N .
BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2002, 25 (07) :931-939
[9]
Mechanism of enhanced hematopoietic response by soluble β-glucan SCG in cyclophosphamide-treated mice [J].
Harada, Toshie ;
Kawaminami, Hiromi ;
Miura, Noriko N. ;
Adachi, Yoshiyuki ;
Nakajima, Mitsuhiro ;
Yadomae, Toshiro ;
Ohno, Naohito .
MICROBIOLOGY AND IMMUNOLOGY, 2006, 50 (09) :687-700
[10]
Mechanism by which orally administered β-1,3-glucans enhance the tumoricidal activity of antitumor monoclonal antibodies in murine tumor models [J].
Hong, F ;
Yan, J ;
Baran, JT ;
Allendorf, DJ ;
Hansen, RD ;
Ostroff, GR ;
Xing, PX ;
Cheung, NKV ;
Ross, GD .
JOURNAL OF IMMUNOLOGY, 2004, 173 (02) :797-806