| Project/Area Number |
06558089
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| Research Category |
Grant-in-Aid for Scientific Research (A)
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| Allocation Type | Single-year Grants |
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| Section | 試験 |
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| Research Field |
Bioorganic chemistry
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| Research Institution | HOKKAIDO UNIVERSITY |
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Principal Investigator |
KOBAYASHI Junichi Hokkaido Univ., Fac.Pharm.Sci., Professor, 薬学部, 教授 (90221241)
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| Co-Investigator(Kenkyū-buntansha) |
SHIGEMORI Hideyuki Hokkaido Univ., Fac.Pharm.Sci., Assistant Professor, 薬学部, 助手 (70202108)
石橋 正己 北海道大学, 薬学部, 助教授 (90212927)
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| Project Period (FY) |
1994 – 1996
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| Project Status |
Completed (Fiscal Year 1996)
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| Budget Amount *help |
¥10,100,000 (Direct Cost: ¥10,100,000)
Fiscal Year 1996: ¥2,200,000 (Direct Cost: ¥2,200,000)
Fiscal Year 1995: ¥2,300,000 (Direct Cost: ¥2,300,000)
Fiscal Year 1994: ¥5,600,000 (Direct Cost: ¥5,600,000)
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| Keywords | MDR modifier / Japanese yew / multidrug-resistance / P-glycoprotein / antitumor / tubulin / P-糖タンパク / 抗がん剤 / イチイ / ジテルペン / タキソ-ル / 海洋天然物 / アルカロイド |
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| Research Abstract |
In this research project, we investigated on search for new compounds to overcome multidrug resistance (MDR) from natural sources.
From the Japanese yew Taxus cuspidata Sieb.et Zucc.collected at Sapporo, 22 new taxoids and related diterpenoids, taxuspines A-H and J-W,were isolated and the structures elucidated on the basis of spectroscopic data and chemical means. Taxuspines B,C,and J increased accumulation of vincristine in multidrug-resistant cells, while taxol did not show such activity. These new taxoids exhibited no cytotoxicity and were not toxic for mice in vivo. These results suggest that some taxoids may become useful lead compounds to overcome multidrug resistance in tumor cells. On the other hand, taxuspine D markedly inhibited Ca^<2+>-induced depolymerization of microtubules and the potency corresponded to half to one third of that of taxol, although taxuspine D lacks both the oxetane ring and N-acylphenylisoserine moiety which are associated with this unique activity in taxol. Taxuspine E,having the oxetane ring but not containing the N-acylphenylisoserine moiety, exhibited potent cytotoxicity against KB tumor cells. More powerful and specific MDR modifiers may be found through further studies of structure-activity relationship on the new compounds obtained in this study.
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