白血球細胞株MOLT-4Fの増殖に対する希少糖D–アロースの抑制効果メカニズムの解析
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- 平田 祐子
- Dept. Cell Physiol., Facult. Med. Univ. Kagawa, Kagawa, Japan
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- 斉藤 まど香
- Schol. Phar. Sincen., Univ. Mukogawa Women's, Hyogo, Japan
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- 塚本 郁子
- Dept. Phar. -Bio-Info., Facult. Med. Univ. Kagawa, Kagawa, Japan
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- 大家 美弥子
- Dept. Phar. -Bio-Info., Facult. Med. Univ. Kagawa, Kagawa, Japan
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- 山口 文徳
- Dept. Cell Physiol., Facult. Med. Univ. Kagawa, Kagawa, Japan
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- 隋 麗
- Dept. Phar. -Bio-Info., Facult. Med. Univ. Kagawa, Kagawa, Japan
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- 神鳥 和代
- Dept. Cell Physiol., Facult. Med. Univ. Kagawa, Kagawa, Japan
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- 小西 良士
- Dept. Phar. -Bio-Info., Facult. Med. Univ. Kagawa, Kagawa, Japan
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- 徳田 雅昭
- Dept. Cell Physiol., Facult. Med. Univ. Kagawa, Kagawa, Japan
書誌事項
- タイトル別名
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- Analysis of the inhibitory mechanism of the rare sugar D-allose on MOLT-4F leukemia cell proliferation.
- 公開日
- 2008
- DOI
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- 10.14849/psjproc.2008.0_201_4
- 公開者
- 一般社団法人 日本生理学会
説明
D-Allose, the C-3 epimer of D-glucose, is one of the rare sugars which occurs rarely in nature. D-Allose was shown to have the most potent inhibitory effect among all rare hexoses on cell proliferation of various human cancer cells. In particular, various lymphoma cell lines have been elucidated to have different susceptibility to D-allose. In other words, the proliferation of some human leukemia cell lines was significantly inhibited by D-allose, and some were not. We chose 5 leukemia cell lines, and found that MOLT-4F has the highest susceptibility to D-allose. Then, we investigated the effect of D-allose on MOLT-4F and Daudi cells which possess the highest and lowest sensitivity to D-allose, respectively. We examined three points: (i) alteration of the D-glucose uptake by D-allose; (ii) incorporation of D-allose into cells; (iii) protein or gene expression altered by D-allose. We found that D-glucose utilization was significantly inhibited by D-allose. However the addition of excess amount of D-glucose in the medium could not abolish the inhibition. These results were suggested the important role of this protein in the effect of D-allose. We found that TXNIP gene expression and its protein expression were specifically and markedly enhanced in MOLT-4F cells by D-allose. This may explain the susceptibility of MOLF-4F cells to D-allose. [J Physiol Sci. 2008;58 Suppl:S201]
収録刊行物
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- 日本生理学会大会発表要旨集
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日本生理学会大会発表要旨集 2008 (0), 201-201, 2008
一般社団法人 日本生理学会
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詳細情報 詳細情報について
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- CRID
- 1390282680706479360
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- NII論文ID
- 130005449815
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- データソース種別
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- JaLC
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可

