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  1. 原著論文

Urokinase-targeted fusion by oncolytic Sendai virus eradicates orthotopic glioblastomas by pronounced synergy with interferon-beta gene

https://repo.qst.go.jp/records/46094
https://repo.qst.go.jp/records/46094
35f8b508-5c8d-47e5-b916-963a8fcad548
Item type 学術雑誌論文 / Journal Article(1)
公開日 2011-06-06
タイトル
タイトル Urokinase-targeted fusion by oncolytic Sendai virus eradicates orthotopic glioblastomas by pronounced synergy with interferon-beta gene
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Hasegawa, Yuzo

× Hasegawa, Yuzo

WEKO 458886

Hasegawa, Yuzo

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Iwadate, Yasuo

× Iwadate, Yasuo

WEKO 458887

Iwadate, Yasuo

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Saito, Shigeyoshi

× Saito, Shigeyoshi

WEKO 458888

Saito, Shigeyoshi

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Aoki, Ichio

× Aoki, Ichio

WEKO 458889

Aoki, Ichio

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Saeki, Naokatsu

× Saeki, Naokatsu

WEKO 458890

Saeki, Naokatsu

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Yonemitsu, Yoshikazu

× Yonemitsu, Yoshikazu

WEKO 458891

Yonemitsu, Yoshikazu

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et.al

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WEKO 458892

et.al

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長谷川 祐三

× 長谷川 祐三

WEKO 458893

en 長谷川 祐三

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岩立 康男

× 岩立 康男

WEKO 458894

en 岩立 康男

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齋藤 茂芳

× 齋藤 茂芳

WEKO 458895

en 齋藤 茂芳

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青木 伊知男

× 青木 伊知男

WEKO 458896

en 青木 伊知男

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抄録
内容記述タイプ Abstract
内容記述 Glioblastoma multiforme (GM), the most frequent primary malignant brain tumor, is highly invasive due to the expression of proteases, including urokinase-type plasminogen activator (uPA). Here, we show the potential of our new and powerful recombinant Sendai virus (rSeV) showing uPA-specific cell-to-cell fusion activity [rSeV/dMFct14 (uPA2), named "BioKnife"] for GM treatment, an effect that was synergistically enhanced by arming BioKnife with the interferon-beta (IFN-beta) gene. BioKnife killed human GM cell lines efficiently in a uPA-dependent fashion, and this killing was prevented by PA inhibitor-1. Rat gliosarcoma 9L cells expressing both uPA and its functional receptor uPAR (9L-L/R) exhibited high uPA activity on the cellular surface and were highly susceptible to BioKnife. Although parent 9L cells (9L-P) were resistant to BioKnife and to BioKnife expressing IFN-beta (BioKnife-IFNbeta), cell-cell fusion of 9L-L/R strongly facilitated the expression of IFN-beta, and in turn, IFN-beta significantly accelerated the fusion activity of BioKnife. A similar synergy was seen in a rat orthotopic brain GM model with 9L-L/R in vivo; therefore, these results suggest that BioKnife-IFNbeta may have significant potential to improve the survival of GM patients in a clinical setting.
書誌情報 Molecular Therapy

巻 18, 号 10, p. 1778-1786, 発行日 2010-07
ISSN
収録物識別子タイプ ISSN
収録物識別子 1525-0016
DOI
識別子タイプ DOI
関連識別子 10.1038/mt.2010.138
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