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3-D浸潤性獲得と上皮形態形成制御を基盤とする腫瘍悪性化機構の研究
https://doi.org/10.24517/00034479
https://doi.org/10.24517/00034479d4734e05-ddc2-4832-8e79-b33440fda57f
名前 / ファイル | ライセンス | アクション |
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CA-PR-MATSUMOTO-K-kaken 2015-6p.pdf (567.9 kB)
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Item type | 報告書 / Research Paper(1) | |||||
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公開日 | 2017-10-05 | |||||
タイトル | ||||||
タイトル | 3-D浸潤性獲得と上皮形態形成制御を基盤とする腫瘍悪性化機構の研究 | |||||
タイトル | ||||||
言語 | en | |||||
タイトル | Mechanisms for malignant tumor progression based on acquisition of 3-D invesiveness and regulation of epithelial morphogenesis | |||||
言語 | ||||||
言語 | jpn | |||||
資源タイプ | ||||||
資源タイプ識別子 | http://purl.org/coar/resource_type/c_18ws | |||||
資源タイプ | research report | |||||
ID登録 | ||||||
ID登録 | 10.24517/00034479 | |||||
ID登録タイプ | JaLC | |||||
著者別表示 |
Matsumoto, Kunio
× Matsumoto, Kunio |
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提供者所属 | ||||||
内容記述タイプ | Other | |||||
内容記述 | 金沢大学がん進展制御研究所 | |||||
書誌情報 |
平成26(2014)年度 科学研究費補助金 基盤研究(B) 研究成果報告書 en : 2014 Fiscal Year Final Research Report 巻 2012-04-01 – 2015-03-31, p. 6p., 発行日 2015-06-08 |
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抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | がん細胞の高い浸潤性はがん転移につながる。本研究は、がん細胞における浸潤能獲得機構をエピジェネティック制御異常ならびにHGF-Met系シグナル特性から明らかにするとともに、HGF-Met相互作用を基盤として人工Met制御分子の創製を目的とした。その結果、(1) PRC複合体構成分子のタンパク質分解異常による機能破綻が、MMP-2を含む浸潤関連遺伝子の発現OFF→ONに関与すること、(2) Met-low→Met-highへの階層的発現変化が悪性黒色種の腫瘍成長、浸潤・転移性に関与することを明らかにするとともに、(3) 環状ペプチド性人工Met-アゴニスト/人工HGFの創製に成功した。 | |||||
抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | Tumor invasion, a typical characteristic of malignant tumors, is regulated not only by intrinsic gene expression profile but also extracellular factors. Met activation by HGF participates in tissue regeneration and tumor invasion. We here found that 1) aberrant proteasome-mediated proteolysis in PRC complex participates in activation of genes (e.g., MMP-2) involved in acquisition of 3-D invasiveness in human malignant mesothelioma cells, and 2) Met expression is regulated by hierarchal equilibrium between Met-low and Met-high populations in malignant melanoma cells, by which invasive and metastatic characteristics is conferred. Based on background for HGF-Met protein-protein interactions, Met-binding cyclic peptides were obtained by RaPID system, and the dimerized peptides induced Met activation and Met-mediated biological responses, in indistinguishable ability to HGF. Thus, we succeeded in generation of artificial Met-agonist / artificial HGF composed of macrocyclic peptide. | |||||
内容記述 | ||||||
内容記述タイプ | Other | |||||
内容記述 | 研究課題/領域番号:24300329, 研究期間(年度):2012-04-01 – 2015-03-31 | |||||
内容記述 | ||||||
内容記述タイプ | Other | |||||
内容記述 | 出典:研究課題「3-D浸潤性獲得と上皮形態形成制御を基盤とする腫瘍悪性化機構の研究」課題番号24300329 (KAKEN:科学研究費助成事業データベース(国立情報学研究所)) (https://kaken.nii.ac.jp/report/KAKENHI-PROJECT-24300329/24300329seika/)を加工して作成 |
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著者版フラグ | ||||||
出版タイプ | AM | |||||
出版タイプResource | http://purl.org/coar/version/c_ab4af688f83e57aa | |||||
関連URI | ||||||
識別子タイプ | URI | |||||
関連識別子 | https://kaken.nii.ac.jp/search/?qm=90201780 | |||||
関連名称 | https://kaken.nii.ac.jp/search/?qm=90201780 | |||||
関連URI | ||||||
識別子タイプ | URI | |||||
関連識別子 | https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-24300329/ | |||||
関連名称 | https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-24300329/ | |||||
関連URI | ||||||
識別子タイプ | URI | |||||
関連識別子 | https://kaken.nii.ac.jp/report/KAKENHI-PROJECT-24300329/24300329seika/ | |||||
関連名称 | https://kaken.nii.ac.jp/report/KAKENHI-PROJECT-24300329/24300329seika/ |