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  1. 医歯学総合研究科
  2. 医歯学総合研究科・学術誌論文

Suppression of Osteosarcoma Cell Invasion by Chemotherapy Is Mediated by Urokinase Plasminogen Activator Activity via Up-Regulation of EGR1

http://hdl.handle.net/10232/19982
http://hdl.handle.net/10232/19982
7169c4cd-dfb6-467b-87b1-7a9ecb095657
名前 / ファイル ライセンス アクション
Suppression Suppression of Osteosarcoma Cell Invasion by Chemotherapy Is Mediated by Urokinase Plasminogen Activator Activity via Up-Regulation of EGR1.pdf (747.5 kB)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2014-02-10
タイトル
タイトル Suppression of Osteosarcoma Cell Invasion by Chemotherapy Is Mediated by Urokinase Plasminogen Activator Activity via Up-Regulation of EGR1
タイトル言語 en
著者 松野下, 幸弘

× 松野下, 幸弘

WEKO 117739

en Matsunoshita, Yukihiro

ja-Kana マツノシタ, ユキヒロ

ja 松野下, 幸弘

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井尻, 幸成

× 井尻, 幸成

WEKO 117740

en Ijiri, Kosei

ja-Kana イジリ, コウセイ

ja 井尻, 幸成

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石堂, 康弘

× 石堂, 康弘

WEKO 117741

en Ishidou, Yasuhiro

ja-Kana イシドウ, ヤスヒロ

ja 石堂, 康弘

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永野, 聡

× 永野, 聡

WEKO 117742

en Nagano, Satoshi

ja-Kana ナガノ, サトシ

ja 永野, 聡

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山元, 拓哉

× 山元, 拓哉

WEKO 117743

en Yamamoto, Takuya

ja-Kana ヤマモト, タクヤ

ja 山元, 拓哉

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永尾, 宗子

× 永尾, 宗子

WEKO 117744

en Nagao, Hiroko

ja-Kana ナガオ, ヒロコ

ja 永尾, 宗子

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小宮, 節郎

× 小宮, 節郎

WEKO 117745

en Komiya, Setsuro

ja-Kana コミヤ, セツロウ

ja 小宮, 節郎

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瀬戸口, 啓夫

× 瀬戸口, 啓夫

WEKO 117746

en Setoguchi, Takao

ja-Kana セトグチ, タカオ

ja 瀬戸口, 啓夫

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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
要約
内容記述タイプ Other
内容記述 Background: The cellular and molecular mechanisms of tumour response following chemotherapy are largely unknown. We found that low dose anti-tumour agents up-regulate early growth response 1 (EGR1) expression. EGR1 is a member of the immediate-early gene group of transcription factors which modulate transcription of multiple genes involved in cell proliferation, differentiation, and development. It has been reported that EGR1 act as either tumour promoting factor or suppressor. We therefore examined the expression and function of EGR1 in osteosarcoma.
Methods: We investigated the expression of EGR1 in human osteosarcoma cell lines and biopsy specimens. We next examined the expression of EGR1 following anti-tumour agents treatment. To examine the function of EGR1 in osteosarcoma, we assessed the tumour growth and invasion in vitro and in vivo.
Results: Real-time PCR revealed that EGR1 was down-regulated both in osteosarcoma cell lines and osteosarcoma patients’ biopsy specimens. In addition, EGR1 was up-regulated both in osteosarcoma patient’ specimens and osteosarcoma cell lines following anti-tumour agent treatment. Although forced expression of EGR1 did not prevent osteosarcoma growth, forced expression of EGR1 prevented osteosarcoma cell invasion in vitro. In addition, forced expression of EGR1 promoted downregulation of urokinase plasminogen activator, urokinase receptor, and urokinase plasminogen activity. Xenograft mice models showed that forced expression of EGR1 prevents osteosarcoma cell migration into blood vessels.
Conclusions: These findings suggest that although chemotherapy could not prevent osteosarcoma growth in chemotherapy-resistant patients, it did prevent osteosarcoma cell invasion by down-regulation of urokinase plasminogen activity via up-regulation of EGR1 during chemotherapy periods.
内容記述言語 en
収録雑誌名 en : PLoS ONE

巻 6, 号 1, 発行日 2011
作成日
日付 2011-01-20
日付タイプ Issued
ISSN
収録物識別子タイプ EISSN
ISSN 19326203
DOI
識別子タイプ DOI
DOI https://doi.org/10.1371/journal.pone.0016234
権利
権利情報の言語 en
権利情報 © 2011 Matsunoshita et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
出版タイプ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
NDC
主題Scheme NDC
主題 493.6
公開者・出版者
出版者 Public Library of Science
出版者言語 en
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