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Emergence of heterogeneity in acute leukemias
BACKGROUND: Leukemias are malignant proliferative disorders of the blood forming system. Sequencing studies demonstrate that the leukemic cell population consists of multiple clones. The genetic relationship between the different clones, referred to as the clonal hierarchy, shows high interindividua...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5062896/ https://www.ncbi.nlm.nih.gov/pubmed/27733173 http://dx.doi.org/10.1186/s13062-016-0154-1 |
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author | Stiehl, Thomas Lutz, Christoph Marciniak-Czochra, Anna |
author_facet | Stiehl, Thomas Lutz, Christoph Marciniak-Czochra, Anna |
author_sort | Stiehl, Thomas |
collection | PubMed |
description | BACKGROUND: Leukemias are malignant proliferative disorders of the blood forming system. Sequencing studies demonstrate that the leukemic cell population consists of multiple clones. The genetic relationship between the different clones, referred to as the clonal hierarchy, shows high interindividual variability. So far, the source of this heterogeneity and its clinical relevance remain unknown. We propose a mathematical model to study the emergence and evolution of clonal heterogeneity in acute leukemias. The model allows linking properties of leukemic clones in terms of self-renewal and proliferation rates to the structure of the clonal hierarchy. RESULTS: Computer simulations imply that the self-renewal potential of the first emerging leukemic clone has a major impact on the total number of leukemic clones and on the structure of their hierarchy. With increasing depth of the clonal hierarchy the self-renewal of leukemic clones increases, whereas the proliferation rates do not change significantly. The emergence of deep clonal hierarchies is a complex process that is facilitated by a cooperativity of different mutations. CONCLUSION: Comparison of patient data and simulation results suggests that the self-renewal of leukemic clones increases with the emergence of clonal heterogeneity. The structure of the clonal hierarchy may serve as a marker for patient prognosis. REVIEWERS: This article was reviewed by Marek Kimmel, Tommaso Lorenzi and Tomasz Lipniacki. |
format | Online Article Text |
id | pubmed-5062896 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-50628962016-10-24 Emergence of heterogeneity in acute leukemias Stiehl, Thomas Lutz, Christoph Marciniak-Czochra, Anna Biol Direct Research BACKGROUND: Leukemias are malignant proliferative disorders of the blood forming system. Sequencing studies demonstrate that the leukemic cell population consists of multiple clones. The genetic relationship between the different clones, referred to as the clonal hierarchy, shows high interindividual variability. So far, the source of this heterogeneity and its clinical relevance remain unknown. We propose a mathematical model to study the emergence and evolution of clonal heterogeneity in acute leukemias. The model allows linking properties of leukemic clones in terms of self-renewal and proliferation rates to the structure of the clonal hierarchy. RESULTS: Computer simulations imply that the self-renewal potential of the first emerging leukemic clone has a major impact on the total number of leukemic clones and on the structure of their hierarchy. With increasing depth of the clonal hierarchy the self-renewal of leukemic clones increases, whereas the proliferation rates do not change significantly. The emergence of deep clonal hierarchies is a complex process that is facilitated by a cooperativity of different mutations. CONCLUSION: Comparison of patient data and simulation results suggests that the self-renewal of leukemic clones increases with the emergence of clonal heterogeneity. The structure of the clonal hierarchy may serve as a marker for patient prognosis. REVIEWERS: This article was reviewed by Marek Kimmel, Tommaso Lorenzi and Tomasz Lipniacki. BioMed Central 2016-10-12 /pmc/articles/PMC5062896/ /pubmed/27733173 http://dx.doi.org/10.1186/s13062-016-0154-1 Text en © The Author(s) 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Stiehl, Thomas Lutz, Christoph Marciniak-Czochra, Anna Emergence of heterogeneity in acute leukemias |
title | Emergence of heterogeneity in acute leukemias |
title_full | Emergence of heterogeneity in acute leukemias |
title_fullStr | Emergence of heterogeneity in acute leukemias |
title_full_unstemmed | Emergence of heterogeneity in acute leukemias |
title_short | Emergence of heterogeneity in acute leukemias |
title_sort | emergence of heterogeneity in acute leukemias |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5062896/ https://www.ncbi.nlm.nih.gov/pubmed/27733173 http://dx.doi.org/10.1186/s13062-016-0154-1 |
work_keys_str_mv | AT stiehlthomas emergenceofheterogeneityinacuteleukemias AT lutzchristoph emergenceofheterogeneityinacuteleukemias AT marciniakczochraanna emergenceofheterogeneityinacuteleukemias |