ミトコンドリア内葉酸代謝酵素を標的としたがん治療
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- 西村 建徳
- 金沢大学 がん進展制御研究所 分子病態研究分野
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- Jin Lee
- 金沢大学 がん進展制御研究所 分子病態研究分野
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- Xiaoxi Chen
- 金沢大学 がん進展制御研究所 分子病態研究分野
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- 東條 有伸
- 東京大学 医科学研究所 先端医療研究センター 分子療法分野
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- 後藤 典子
- 金沢大学 がん進展制御研究所 分子病態研究分野
書誌事項
- タイトル別名
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- Cancer treatments targeting mitochondrial enzymes involved in one-carbon metabolism
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<p>One-carbon metabolism, also called folate-mediated metabolism, has been targeted for the treatment of patients with cancer. However, therapeutic windows available to the inhibitors of one-carbon metabolism are limited and some patients have been shown to develop resistance to anti-folate drugs. Recently, we showed that mitochondrial enzymes involved in one-carbon metabolism have greater specifi city toward cancer cells than the cytoplasmic enzymes. In our study, we knocked down the methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2, methenyltetrahydrofolate cyclohydrolase (MTHFD2) gene in order to inhibit the activity of one such mitochondrial enzyme. Cell cycle progression was analyzed using propidium iodide, and stem cell-like nature was evaluated in terms of aldehyde dehydrogenase activity on a fl ow cytometric setup. Our results showed a drastic decrease in cellular proliferation and stem cell-like phenotypes in the MTHFD2 knockdown cells. From a mechanistic point of view, the inhibition of cellular growth could be predominantly ascribed to the depletion of purine nucleotides, and that of stem cell-like phenotypes was attributable to the accumulation of 1-(5'-phosphoribosyl)-5-amino-4- imidazolecarboxamide.</p>
収録刊行物
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- サイトメトリーリサーチ
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サイトメトリーリサーチ 30 (2), 9-13, 2020-12-11
日本サイトメトリー学会
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詳細情報 詳細情報について
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- CRID
- 1391975831218432128
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- NII論文ID
- 130007952546
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- ISSN
- 24240664
- 09166920
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- 本文言語コード
- ja
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- データソース種別
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- JaLC
- CiNii Articles
- KAKEN
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- 抄録ライセンスフラグ
- 使用不可