Abstract

BackgroundLeukemias 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.ResultsComputer 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.ConclusionComparison 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.ReviewersThis article was reviewed by Marek Kimmel, Tommaso Lorenzi and Tomasz Lipniacki.

Highlights

  • Leukemias are malignant proliferative disorders of the blood forming system

  • In the remaining 5 % of simulated patients, the following phenomena have been observed: (i) in very rare cases a slight reduction in the self-renewal rate is compensated by an increase in proliferation rate, (ii) two new clones emerge within a short time span, the selfrenewal rate of both clones is larger than the self-renewal rate of the parent clones, but one of the emerging clones has a slightly reduced self-renewal rate compared to the other

  • When a new clone arises due to a mutation, its self-renewal and proliferation rates can be larger or smaller than the corresponding rates of the parent clone

Read more

Summary

Introduction

Leukemias are malignant proliferative disorders of the blood forming system. Sequencing studies demonstrate that the leukemic cell population consists of multiple clones. Acute leukemias are clonal diseases of the blood forming (hematopoietic) system. They lead to expansion of malignant cells and resulting impairment of blood cell formation. Over the last years evidence has accumulated that many leukemia subtypes are maintained by a subpopulation of cells with stem cell-like properties [1,2,3]. These cells are referred to as leukemic stem cells (LSCs) or leukemia initiating cells (LICs) and potentially trigger relapse of the disease [4, 5].

Methods
Results
Discussion
Conclusion

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.