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  1. 原著論文

Multiple Administrations of 64Cu-ATSM as a Novel Therapeutic Option for Glioblastoma: a Translational Study Using Mice with Xenografts

https://repo.qst.go.jp/records/48558
https://repo.qst.go.jp/records/48558
7384c95a-78f0-4483-9e75-6fc1a2de543a
Item type 学術雑誌論文 / Journal Article(1)
公開日 2018-03-08
タイトル
タイトル Multiple Administrations of 64Cu-ATSM as a Novel Therapeutic Option for Glioblastoma: a Translational Study Using Mice with Xenografts
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 Yoshii, Yukie

× Yoshii, Yukie

WEKO 488263

Yoshii, Yukie

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Hiroki Matsumoto

× Hiroki Matsumoto

WEKO 488264

Hiroki Matsumoto

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Yoshimoto, Mitsuyoshi

× Yoshimoto, Mitsuyoshi

WEKO 488265

Yoshimoto, Mitsuyoshi

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Zhang, Ming-Rong

× Zhang, Ming-Rong

WEKO 488266

Zhang, Ming-Rong

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Ooe, Yoko

× Ooe, Yoko

WEKO 488267

Ooe, Yoko

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Kurihara, Hiroaki

× Kurihara, Hiroaki

WEKO 488268

Kurihara, Hiroaki

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Narita, Yoshitaka

× Narita, Yoshitaka

WEKO 488269

Narita, Yoshitaka

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Jin, Zhao-Hui

× Jin, Zhao-Hui

WEKO 488270

Jin, Zhao-Hui

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Tsuji, Atsushi

× Tsuji, Atsushi

WEKO 488271

Tsuji, Atsushi

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Yoshinaga, Keiichiro

× Yoshinaga, Keiichiro

WEKO 488272

Yoshinaga, Keiichiro

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Fujibayashi, Yasuhisa

× Fujibayashi, Yasuhisa

WEKO 488273

Fujibayashi, Yasuhisa

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Higashi, Tatsuya

× Higashi, Tatsuya

WEKO 488274

Higashi, Tatsuya

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吉井 幸恵

× 吉井 幸恵

WEKO 488275

en 吉井 幸恵

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張 明栄

× 張 明栄

WEKO 488276

en 張 明栄

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大江 洋子

× 大江 洋子

WEKO 488277

en 大江 洋子

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金 朝暉

× 金 朝暉

WEKO 488278

en 金 朝暉

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辻 厚至

× 辻 厚至

WEKO 488279

en 辻 厚至

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吉永 恵一郎

× 吉永 恵一郎

WEKO 488280

en 吉永 恵一郎

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藤林 康久

× 藤林 康久

WEKO 488281

en 藤林 康久

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東 達也

× 東 達也

WEKO 488282

en 東 達也

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抄録
内容記述タイプ Abstract
内容記述 Glioblastoma is the most aggressive malignant brain tumor in humans and is difficult to cure using current
treatment options. Hypoxic regions are frequently found in glioblastoma, and increased levels of hypoxia are
associated with poor clinical outcomes of glioblastoma patients. Hypoxia plays important roles in the progression
and recurrence of glioblastoma because of drug delivery deficiencies and induction of hypoxia-inducible factor-1α
in tumor cells, which lead to poor prognosis. We focused on a promising hypoxia-targeted internal radiotherapy
agent, 64Cu-diacetyl-bis (N4-methylthiosemicarbazone) (64Cu-ATSM), to address the need for additional treatment
for glioblastoma. This compound can target the overreduced state under hypoxic conditions within tumors.
Clinical positron emission tomography studies using radiolabeled Cu-ATSM have shown that Cu-ATSM
accumulates in glioblastoma and its uptake is associated with high hypoxia-inducible factor-1α expression. To
evaluate the therapeutic potential of this agent for glioblastoma, we examined the efficacy of 64Cu-ATSM in mice
bearing U87MG glioblastoma tumors. Administration of single dosage (18.5, 37, 74, 111, and 148 MBq) and
multiple dosages (37 MBq × 4) of 64Cu-ATSM was investigated. Single administration of 64Cu-ATSM in high-dose
groups dose-dependently inhibited tumor growth and prolonged survival, with slight and reverse signs of adverse
events. Multiple dosages of 64Cu-ATSM remarkably inhibited tumor growth and prolonged survival. By splitting the
dose of 64Cu-ATSM, no adverse effects were observed. Our findings indicate that multiple administrations of
64Cu-ATSM have effective antitumor effects in glioblastoma without side effects, indicating its potential for
treating this fatal disease.
書誌情報 Translational Oncology

巻 11, 号 1, p. 24-30, 発行日 2017-11
出版者
出版者 ELSEVIER
PubMed番号
識別子タイプ PMID
関連識別子 29154146
DOI
識別子タイプ DOI
関連識別子 10.1016/j.tranon.2017.10.006
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