このアイテムのアクセス数: 109
このアイテムのファイル:
ファイル | 記述 | サイズ | フォーマット | |
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cas.15506.pdf | 3.49 MB | Adobe PDF | 見る/開く |
完全メタデータレコード
DCフィールド | 値 | 言語 |
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dc.contributor.author | Tanaka, Kuniaki | en |
dc.contributor.author | Kato, Itaru | en |
dc.contributor.author | Dobashi, Yuu | en |
dc.contributor.author | Imai, Jun‐ichi | en |
dc.contributor.author | Mikami, Takashi | en |
dc.contributor.author | Kubota, Hirohito | en |
dc.contributor.author | Ueno, Hiroo | en |
dc.contributor.author | Ito, Mamoru | en |
dc.contributor.author | Ogawa, Seishi | en |
dc.contributor.author | Nakahata, Tatsutoshi | en |
dc.contributor.author | Takita, Junko | en |
dc.contributor.author | Toyoda, Hidemi | en |
dc.contributor.author | Ogawa, Chitose | en |
dc.contributor.author | Adachi, Souichi | en |
dc.contributor.author | Watanabe, Shinya | en |
dc.contributor.author | Goto, Hiroaki | en |
dc.contributor.alternative | 田中, 邦明 | ja |
dc.contributor.alternative | 加藤, 格 | ja |
dc.contributor.alternative | 三上, 貴司 | ja |
dc.contributor.alternative | 窪田, 博仁 | ja |
dc.contributor.alternative | 上野, 浩生 | ja |
dc.contributor.alternative | 小川, 誠司 | ja |
dc.contributor.alternative | 中畑, 龍俊 | ja |
dc.contributor.alternative | 滝田, 順子 | ja |
dc.contributor.alternative | 足立, 壯一 | ja |
dc.date.accessioned | 2023-06-01T05:03:32Z | - |
dc.date.available | 2023-06-01T05:03:32Z | - |
dc.date.issued | 2022-11 | - |
dc.identifier.uri | http://hdl.handle.net/2433/283090 | - |
dc.description.abstract | A lack of practical resources in Japan has limited preclinical discovery and testing of therapies for pediatric relapsed and refractory acute lymphoblastic leukemia (ALL), which has poor outcomes. Here, we established 57 patient-derived xenografts (PDXs) in NOD.Cg-Prkdcscidll2rgtm1Sug/ShiJic (NOG) mice and created a biobank by preserving PDX cells including three extramedullary relapsed ALL PDXs. We demonstrated that our PDX mice and PDX cells mimicked the biological features of relapsed ALL and that PDX models reproduced treatment-mediated clonal selection. Our PDX biobank is a useful scientific resource for capturing drug sensitivity features of pediatric patients with ALL, providing an essential tool for the development of targeted therapies. | en |
dc.language.iso | eng | - |
dc.publisher | Wiley | en |
dc.publisher | Japanese Cancer Association | en |
dc.rights | © 2022 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. | en |
dc.rights | This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. | en |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | - |
dc.subject | biobank | en |
dc.subject | leukemia | en |
dc.subject | pediatric | en |
dc.subject | preclinical | en |
dc.subject | xenograft | en |
dc.title | The first Japanese biobank of patient‐derived pediatric acute lymphoblastic leukemia xenograft models | en |
dc.type | journal article | - |
dc.type.niitype | Journal Article | - |
dc.identifier.jtitle | Cancer Science | en |
dc.identifier.volume | 113 | - |
dc.identifier.issue | 11 | - |
dc.identifier.spage | 3814 | - |
dc.identifier.epage | 3825 | - |
dc.relation.doi | 10.1111/cas.15506 | - |
dc.textversion | publisher | - |
dc.identifier.pmid | 35879192 | - |
dcterms.accessRights | open access | - |
dc.identifier.pissn | 1347-9032 | - |
dc.identifier.eissn | 1349-7006 | - |
出現コレクション: | 学術雑誌掲載論文等 |

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