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The first Japanese biobank of patient‐derived pediatric acute lymphoblastic leukemia xenograft models
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‐Prkdc ( scid ) ll2rg ( tm1Sug )/Shi...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9633318/ https://www.ncbi.nlm.nih.gov/pubmed/35879192 http://dx.doi.org/10.1111/cas.15506 |
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author | Tanaka, Kuniaki Kato, Itaru Dobashi, Yuu Imai, Jun‐ichi Mikami, Takashi Kubota, Hirohito Ueno, Hiroo Ito, Mamoru Ogawa, Seishi Nakahata, Tatsutoshi Takita, Junko Toyoda, Hidemi Ogawa, Chitose Adachi, Souichi Watanabe, Shinya Goto, Hiroaki |
author_facet | Tanaka, Kuniaki Kato, Itaru Dobashi, Yuu Imai, Jun‐ichi Mikami, Takashi Kubota, Hirohito Ueno, Hiroo Ito, Mamoru Ogawa, Seishi Nakahata, Tatsutoshi Takita, Junko Toyoda, Hidemi Ogawa, Chitose Adachi, Souichi Watanabe, Shinya Goto, Hiroaki |
author_sort | Tanaka, Kuniaki |
collection | PubMed |
description | 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‐Prkdc ( scid ) ll2rg ( tm1Sug )/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. |
format | Online Article Text |
id | pubmed-9633318 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96333182022-11-07 The first Japanese biobank of patient‐derived pediatric acute lymphoblastic leukemia xenograft models Tanaka, Kuniaki Kato, Itaru Dobashi, Yuu Imai, Jun‐ichi Mikami, Takashi Kubota, Hirohito Ueno, Hiroo Ito, Mamoru Ogawa, Seishi Nakahata, Tatsutoshi Takita, Junko Toyoda, Hidemi Ogawa, Chitose Adachi, Souichi Watanabe, Shinya Goto, Hiroaki Cancer Sci Original Articles 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‐Prkdc ( scid ) ll2rg ( tm1Sug )/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. John Wiley and Sons Inc. 2022-08-30 2022-11 /pmc/articles/PMC9633318/ /pubmed/35879192 http://dx.doi.org/10.1111/cas.15506 Text en © 2022 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) 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. |
spellingShingle | Original Articles Tanaka, Kuniaki Kato, Itaru Dobashi, Yuu Imai, Jun‐ichi Mikami, Takashi Kubota, Hirohito Ueno, Hiroo Ito, Mamoru Ogawa, Seishi Nakahata, Tatsutoshi Takita, Junko Toyoda, Hidemi Ogawa, Chitose Adachi, Souichi Watanabe, Shinya Goto, Hiroaki The first Japanese biobank of patient‐derived pediatric acute lymphoblastic leukemia xenograft models |
title | The first Japanese biobank of patient‐derived pediatric acute lymphoblastic leukemia xenograft models |
title_full | The first Japanese biobank of patient‐derived pediatric acute lymphoblastic leukemia xenograft models |
title_fullStr | The first Japanese biobank of patient‐derived pediatric acute lymphoblastic leukemia xenograft models |
title_full_unstemmed | The first Japanese biobank of patient‐derived pediatric acute lymphoblastic leukemia xenograft models |
title_short | The first Japanese biobank of patient‐derived pediatric acute lymphoblastic leukemia xenograft models |
title_sort | first japanese biobank of patient‐derived pediatric acute lymphoblastic leukemia xenograft models |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9633318/ https://www.ncbi.nlm.nih.gov/pubmed/35879192 http://dx.doi.org/10.1111/cas.15506 |
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