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Quinacrine-CASIN combination overcomes chemoresistance in human acute lymphoid leukemia
Chemoresistance posts a major hurdle for treatment of acute leukemia. There is increasing evidence that prolonged and intensive chemotherapy often fails to eradicate leukemic stem cells, which are protected by the bone marrow niche and can induce relapse. Thus, new therapeutic approaches to overcome...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8626516/ https://www.ncbi.nlm.nih.gov/pubmed/34836965 http://dx.doi.org/10.1038/s41467-021-27300-w |
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author | Wu, Limei Chatla, Srinivas Lin, Qiqi Chowdhury, Fabliha Ahmed Geldenhuys, Werner Du, Wei |
author_facet | Wu, Limei Chatla, Srinivas Lin, Qiqi Chowdhury, Fabliha Ahmed Geldenhuys, Werner Du, Wei |
author_sort | Wu, Limei |
collection | PubMed |
description | Chemoresistance posts a major hurdle for treatment of acute leukemia. There is increasing evidence that prolonged and intensive chemotherapy often fails to eradicate leukemic stem cells, which are protected by the bone marrow niche and can induce relapse. Thus, new therapeutic approaches to overcome chemoresistance are urgently needed. By conducting an ex vivo small molecule screen, here we have identified Quinacrine (QC) as a sensitizer for Cytarabine (AraC) in treating acute lymphoblastic leukemia (ALL). We show that QC enhances AraC-mediated killing of ALL cells, and subsequently abrogates AraC resistance both in vitro and in an ALL-xenograft model. However, while combo AraC+QC treatment prolongs the survival of primary transplanted recipients, the combination exhibits limited efficacy in secondary transplanted recipients, consistent with the survival of niche-protected leukemia stem cells. Introduction of Cdc42 Activity Specific Inhibitor, CASIN, enhances the eradication of ALL leukemia stem cells by AraC+QC and prolongs the survival of both primary and secondary transplanted recipients without affecting normal long-term human hematopoiesis. Together, our findings identify a small-molecule regimen that sensitizes AraC-mediated leukemia eradication and provide a potential therapeutic approach for better ALL treatment. |
format | Online Article Text |
id | pubmed-8626516 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-86265162021-12-10 Quinacrine-CASIN combination overcomes chemoresistance in human acute lymphoid leukemia Wu, Limei Chatla, Srinivas Lin, Qiqi Chowdhury, Fabliha Ahmed Geldenhuys, Werner Du, Wei Nat Commun Article Chemoresistance posts a major hurdle for treatment of acute leukemia. There is increasing evidence that prolonged and intensive chemotherapy often fails to eradicate leukemic stem cells, which are protected by the bone marrow niche and can induce relapse. Thus, new therapeutic approaches to overcome chemoresistance are urgently needed. By conducting an ex vivo small molecule screen, here we have identified Quinacrine (QC) as a sensitizer for Cytarabine (AraC) in treating acute lymphoblastic leukemia (ALL). We show that QC enhances AraC-mediated killing of ALL cells, and subsequently abrogates AraC resistance both in vitro and in an ALL-xenograft model. However, while combo AraC+QC treatment prolongs the survival of primary transplanted recipients, the combination exhibits limited efficacy in secondary transplanted recipients, consistent with the survival of niche-protected leukemia stem cells. Introduction of Cdc42 Activity Specific Inhibitor, CASIN, enhances the eradication of ALL leukemia stem cells by AraC+QC and prolongs the survival of both primary and secondary transplanted recipients without affecting normal long-term human hematopoiesis. Together, our findings identify a small-molecule regimen that sensitizes AraC-mediated leukemia eradication and provide a potential therapeutic approach for better ALL treatment. Nature Publishing Group UK 2021-11-26 /pmc/articles/PMC8626516/ /pubmed/34836965 http://dx.doi.org/10.1038/s41467-021-27300-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Wu, Limei Chatla, Srinivas Lin, Qiqi Chowdhury, Fabliha Ahmed Geldenhuys, Werner Du, Wei Quinacrine-CASIN combination overcomes chemoresistance in human acute lymphoid leukemia |
title | Quinacrine-CASIN combination overcomes chemoresistance in human acute lymphoid leukemia |
title_full | Quinacrine-CASIN combination overcomes chemoresistance in human acute lymphoid leukemia |
title_fullStr | Quinacrine-CASIN combination overcomes chemoresistance in human acute lymphoid leukemia |
title_full_unstemmed | Quinacrine-CASIN combination overcomes chemoresistance in human acute lymphoid leukemia |
title_short | Quinacrine-CASIN combination overcomes chemoresistance in human acute lymphoid leukemia |
title_sort | quinacrine-casin combination overcomes chemoresistance in human acute lymphoid leukemia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8626516/ https://www.ncbi.nlm.nih.gov/pubmed/34836965 http://dx.doi.org/10.1038/s41467-021-27300-w |
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