COMPARATIVE STUDY OF ANTITUMOR ACTIVITY AND IMMUNOMODULATORY EFFECT OF TETRAHYDRO-2-FURANYL AND TETRAHYDRO-2-PYRANYL (1→3)-β-D-GLUCANS
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概要
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The effects of tetrahydro-2-furanyl- and tetrahydro-2-pyranyl-ethers of (1→3)-β-D-glucans from Alcaligenes faecalis var.myxogenes (IFO 13140) on the activities of macrophages and natural killer (NK) cells in either ICR or BALB/c mice were studies. The derivatives with strong antitumor activity against Sarcoma 180 in ICR mice induced higher macrophage tumoricidal activity (>40%) than those with low antitumor activity (<20%). All derivatives with high or low antitumor activity augmented NK cell activity. On the other hand, the derivatives which show the high antitumor activity against Meth-A in BALB/c mice enhanced macrophage tumoricidal activity, while those with low or no antitumor activity did not. NK cell activity was activated by the derivatives with or without the antitumor activity. Furthermore, certain derivative which has high antitumor activity against Sarcoma 180 in ICR mice did not increase serum component (LB) in ICR mice. These results indicate that the antitumor activity of the derivatives correlates only with the capacity to cause macrophage actiation in vivo.
- 公益社団法人日本薬学会の論文
著者
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SASAKI TAKUMA
Chemotherapy Division, National Cancer Center Research Institute
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UCHIDA HIROYUKI
Chemotherapy Division, National Cancer Center Research Institute
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Sasaki Takuma
Chemotherapy Division National Cancer Center Research Institute
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Uchida Hiroyuki
Chemotherapy Division National Cancer Center Research Institute
関連論文
- ANTITUMOR ACTIVITY OF AQUEOUS EXTRACTS OF MARIRE ANIMALS
- EFFECT OF SERUM FROM MICE TREATED WITH ANTITUMOR POLYSACCHARIDE ON EXPRESSION OF CYTOTOXICITY BY MOUSE PERITONEAL MACROPHAGES
- COMPARATIVE STUDY OF ANTITUMOR ACTIVITY AND IMMUNOMODULATORY EFFECT OF TETRAHYDRO-2-FURANYL AND TETRAHYDRO-2-PYRANYL (1→3)-β-D-GLUCANS
- A high-resolution solid-state 13C NMR study of (1.RAR.3)-.BETA.-D-glucans from various sources. Conformational characterization as viewed from the conformation-dependent 13C chemical shifts and its consequence to gelation property.