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Zebrafish B cell acute lymphoblastic leukemia: new findings in an old model
Acute lymphoblastic leukemia (ALL) is the most common pediatric, and ninth most common adult, cancer. ALL can develop in either B or T lymphocytes, but B-lineage ALL (B-ALL) exceeds T-ALL clinically. As for other cancers, animal models allow study of the molecular mechanisms driving ALL. Several zeb...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7170496/ https://www.ncbi.nlm.nih.gov/pubmed/32341750 http://dx.doi.org/10.18632/oncotarget.27555 |
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author | Park, Gilseung Burroughs-Garcia, Jessica Foster, Clay A. Hasan, Ameera Borga, Chiara Frazer, J. Kimble |
author_facet | Park, Gilseung Burroughs-Garcia, Jessica Foster, Clay A. Hasan, Ameera Borga, Chiara Frazer, J. Kimble |
author_sort | Park, Gilseung |
collection | PubMed |
description | Acute lymphoblastic leukemia (ALL) is the most common pediatric, and ninth most common adult, cancer. ALL can develop in either B or T lymphocytes, but B-lineage ALL (B-ALL) exceeds T-ALL clinically. As for other cancers, animal models allow study of the molecular mechanisms driving ALL. Several zebrafish (Danio rerio) T-ALL models have been reported, but until recently, robust D. rerio B-ALL models were not described. Then, D. rerio B-ALL was discovered in two related zebrafish transgenic lines; both were already known to develop T-ALL. Here, we report new B-ALL findings in one of these models, fish expressing transgenic human MYC (hMYC). We describe B-ALL incidence in a large cohort of hMYC fish, and show B-ALL in two new lines where T-ALL does not interfere with B-ALL detection. We also demonstrate B-ALL responses to steroid and radiation treatments, which effect ALL remissions, but are usually followed by prompt relapses. Finally, we report gene expression in zebrafish B lymphocytes and B-ALL, in both bulk samples and single B- and T-ALL cells. Using these gene expression profiles, we compare differences between the two new D. rerio B-ALL models, which are both driven by transgenic mammalian MYC oncoproteins. Collectively, these new data expand the utility of this new vertebrate B-ALL model. |
format | Online Article Text |
id | pubmed-7170496 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-71704962020-04-27 Zebrafish B cell acute lymphoblastic leukemia: new findings in an old model Park, Gilseung Burroughs-Garcia, Jessica Foster, Clay A. Hasan, Ameera Borga, Chiara Frazer, J. Kimble Oncotarget Research Perspective Acute lymphoblastic leukemia (ALL) is the most common pediatric, and ninth most common adult, cancer. ALL can develop in either B or T lymphocytes, but B-lineage ALL (B-ALL) exceeds T-ALL clinically. As for other cancers, animal models allow study of the molecular mechanisms driving ALL. Several zebrafish (Danio rerio) T-ALL models have been reported, but until recently, robust D. rerio B-ALL models were not described. Then, D. rerio B-ALL was discovered in two related zebrafish transgenic lines; both were already known to develop T-ALL. Here, we report new B-ALL findings in one of these models, fish expressing transgenic human MYC (hMYC). We describe B-ALL incidence in a large cohort of hMYC fish, and show B-ALL in two new lines where T-ALL does not interfere with B-ALL detection. We also demonstrate B-ALL responses to steroid and radiation treatments, which effect ALL remissions, but are usually followed by prompt relapses. Finally, we report gene expression in zebrafish B lymphocytes and B-ALL, in both bulk samples and single B- and T-ALL cells. Using these gene expression profiles, we compare differences between the two new D. rerio B-ALL models, which are both driven by transgenic mammalian MYC oncoproteins. Collectively, these new data expand the utility of this new vertebrate B-ALL model. Impact Journals LLC 2020-04-14 /pmc/articles/PMC7170496/ /pubmed/32341750 http://dx.doi.org/10.18632/oncotarget.27555 Text en http://creativecommons.org/licenses/by/3.0/ Copyright: Park et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Perspective Park, Gilseung Burroughs-Garcia, Jessica Foster, Clay A. Hasan, Ameera Borga, Chiara Frazer, J. Kimble Zebrafish B cell acute lymphoblastic leukemia: new findings in an old model |
title | Zebrafish B cell acute lymphoblastic leukemia: new findings in an old model |
title_full | Zebrafish B cell acute lymphoblastic leukemia: new findings in an old model |
title_fullStr | Zebrafish B cell acute lymphoblastic leukemia: new findings in an old model |
title_full_unstemmed | Zebrafish B cell acute lymphoblastic leukemia: new findings in an old model |
title_short | Zebrafish B cell acute lymphoblastic leukemia: new findings in an old model |
title_sort | zebrafish b cell acute lymphoblastic leukemia: new findings in an old model |
topic | Research Perspective |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7170496/ https://www.ncbi.nlm.nih.gov/pubmed/32341750 http://dx.doi.org/10.18632/oncotarget.27555 |
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