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A high-throughput screen indicates gemcitabine and JAK inhibitors may be useful for treating pediatric AML

Improvement in survival has been achieved for children and adolescents with AML but is largely attributed to enhanced supportive care as opposed to the development of better treatment regimens. High risk subtypes continue to have poor outcomes with event free survival rates <40% despite the use o...

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Autores principales: Drenberg, Christina D., Shelat, Anang, Dang, Jinjun, Cotton, Anitria, Orwick, Shelley J., Li, Mengyu, Jeon, Jae Yoon, Fu, Qiang, Buelow, Daelynn R., Pioso, Marissa, Hu, Shuiying, Inaba, Hiroto, Ribeiro, Raul C., Rubnitz, Jeffrey E., Gruber, Tanja A., Guy, R. Kiplin, Baker, Sharyn D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6522510/
https://www.ncbi.nlm.nih.gov/pubmed/31097698
http://dx.doi.org/10.1038/s41467-019-09917-0
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author Drenberg, Christina D.
Shelat, Anang
Dang, Jinjun
Cotton, Anitria
Orwick, Shelley J.
Li, Mengyu
Jeon, Jae Yoon
Fu, Qiang
Buelow, Daelynn R.
Pioso, Marissa
Hu, Shuiying
Inaba, Hiroto
Ribeiro, Raul C.
Rubnitz, Jeffrey E.
Gruber, Tanja A.
Guy, R. Kiplin
Baker, Sharyn D.
author_facet Drenberg, Christina D.
Shelat, Anang
Dang, Jinjun
Cotton, Anitria
Orwick, Shelley J.
Li, Mengyu
Jeon, Jae Yoon
Fu, Qiang
Buelow, Daelynn R.
Pioso, Marissa
Hu, Shuiying
Inaba, Hiroto
Ribeiro, Raul C.
Rubnitz, Jeffrey E.
Gruber, Tanja A.
Guy, R. Kiplin
Baker, Sharyn D.
author_sort Drenberg, Christina D.
collection PubMed
description Improvement in survival has been achieved for children and adolescents with AML but is largely attributed to enhanced supportive care as opposed to the development of better treatment regimens. High risk subtypes continue to have poor outcomes with event free survival rates <40% despite the use of high intensity chemotherapy in combination with hematopoietic stem cell transplant. Here we combine high-throughput screening, intracellular accumulation assays, and in vivo efficacy studies to identify therapeutic strategies for pediatric AML. We report therapeutics not currently used to treat AML, gemcitabine and cabazitaxel, have broad anti-leukemic activity across subtypes and are more effective relative to the AML standard of care, cytarabine, both in vitro and in vivo. JAK inhibitors are selective for acute megakaryoblastic leukemia and significantly prolong survival in multiple preclinical models. Our approach provides advances in the development of treatment strategies for pediatric AML.
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spelling pubmed-65225102019-05-20 A high-throughput screen indicates gemcitabine and JAK inhibitors may be useful for treating pediatric AML Drenberg, Christina D. Shelat, Anang Dang, Jinjun Cotton, Anitria Orwick, Shelley J. Li, Mengyu Jeon, Jae Yoon Fu, Qiang Buelow, Daelynn R. Pioso, Marissa Hu, Shuiying Inaba, Hiroto Ribeiro, Raul C. Rubnitz, Jeffrey E. Gruber, Tanja A. Guy, R. Kiplin Baker, Sharyn D. Nat Commun Article Improvement in survival has been achieved for children and adolescents with AML but is largely attributed to enhanced supportive care as opposed to the development of better treatment regimens. High risk subtypes continue to have poor outcomes with event free survival rates <40% despite the use of high intensity chemotherapy in combination with hematopoietic stem cell transplant. Here we combine high-throughput screening, intracellular accumulation assays, and in vivo efficacy studies to identify therapeutic strategies for pediatric AML. We report therapeutics not currently used to treat AML, gemcitabine and cabazitaxel, have broad anti-leukemic activity across subtypes and are more effective relative to the AML standard of care, cytarabine, both in vitro and in vivo. JAK inhibitors are selective for acute megakaryoblastic leukemia and significantly prolong survival in multiple preclinical models. Our approach provides advances in the development of treatment strategies for pediatric AML. Nature Publishing Group UK 2019-05-16 /pmc/articles/PMC6522510/ /pubmed/31097698 http://dx.doi.org/10.1038/s41467-019-09917-0 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Drenberg, Christina D.
Shelat, Anang
Dang, Jinjun
Cotton, Anitria
Orwick, Shelley J.
Li, Mengyu
Jeon, Jae Yoon
Fu, Qiang
Buelow, Daelynn R.
Pioso, Marissa
Hu, Shuiying
Inaba, Hiroto
Ribeiro, Raul C.
Rubnitz, Jeffrey E.
Gruber, Tanja A.
Guy, R. Kiplin
Baker, Sharyn D.
A high-throughput screen indicates gemcitabine and JAK inhibitors may be useful for treating pediatric AML
title A high-throughput screen indicates gemcitabine and JAK inhibitors may be useful for treating pediatric AML
title_full A high-throughput screen indicates gemcitabine and JAK inhibitors may be useful for treating pediatric AML
title_fullStr A high-throughput screen indicates gemcitabine and JAK inhibitors may be useful for treating pediatric AML
title_full_unstemmed A high-throughput screen indicates gemcitabine and JAK inhibitors may be useful for treating pediatric AML
title_short A high-throughput screen indicates gemcitabine and JAK inhibitors may be useful for treating pediatric AML
title_sort high-throughput screen indicates gemcitabine and jak inhibitors may be useful for treating pediatric aml
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6522510/
https://www.ncbi.nlm.nih.gov/pubmed/31097698
http://dx.doi.org/10.1038/s41467-019-09917-0
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