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Genotoxicity of cytokines at chemotherapy-induced 'storm' concentrations in a model of the human bone marrow

Asurappulige, Harshini S H; Thomas, Adam D; Morse, H. Ruth

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Authors

Harshini S H Asurappulige

Adam Thomas Adam7.Thomas@uwe.ac.uk
Senior Lecturer in Human Genetics and Genomics

Dr Ruth Morse Ruth.Morse@uwe.ac.uk
Associate Professor in Biomedical Sciences



Abstract

Donor cell leukaemia (DCL) is a complication of haematopoietic stem cell transplantation where donated cells become malignant within the patient's bone marrow. As DCL predominates as acute myeloid leukaemia, we hypothesized that the cytokine storm following chemotherapy played a role in promoting and supporting leukaemogenesis. Cytokines have also been implicated in genotoxicity; thus, we explored a cell line model of the human bone marrow (BM) to secrete myeloid cytokines following drug treatment and their potential to induce micronuclei. HS-5 human stromal cells were exposed to mitoxantrone (MTX) and chlorambucil (CHL) and, for the first time, were profiled for 80 cytokines using an array. Fifty-four cytokines were detected in untreated cells, of which 24 were upregulated and 10 were downregulated by both drugs. FGF-7 was the lowest cytokine to be detected in both untreated and treated cells. Eleven cytokines not detected at baseline were detected following drug exposure. TNFα, IL6, GM-CSF, G-CSF, and TGFβ1 were selected for micronuclei induction. TK6 cells were exposed to these cytokines in isolation and in paired combinations. Only TNFα and TGFβ1 induced micronuclei at healthy concentrations, but all five cytokines induced micronuclei at storm levels, which was further increased when combined in pairs. Of particular concern was that some combinations induced micronuclei at levels above the mitomycin C positive control; however, most combinations were less than the sum of micronuclei induced following exposure to each cytokine in isolation. These data infer a possible role for cytokines through chemotherapy-induced cytokine storm, in the instigation and support of leukaemogenesis in the BM, and implicate the need to evaluate individuals for variability in cytokine secretion as a potential risk factor for complications such as DCL.

Citation

Asurappulige, H. S. H., Thomas, A. D., & Morse, H. R. (2023). Genotoxicity of cytokines at chemotherapy-induced 'storm' concentrations in a model of the human bone marrow. Mutagenesis, 38(4), 201-215. https://doi.org/10.1093/mutage/gead018

Journal Article Type Article
Acceptance Date Jun 14, 2023
Online Publication Date Jun 16, 2023
Publication Date Jul 31, 2023
Deposit Date Aug 25, 2023
Publicly Available Date Aug 25, 2023
Journal Mutagenesis
Print ISSN 0267-8357
Electronic ISSN 1464-3804
Publisher Oxford University Press (OUP)
Peer Reviewed Peer Reviewed
Volume 38
Issue 4
Pages 201-215
DOI https://doi.org/10.1093/mutage/gead018
Public URL https://uwe-repository.worktribe.com/output/10900232
Publisher URL https://academic.oup.com/mutage/advance-article-abstract/doi/10.1093/mutage/gead018/7199634?utm_source=advanceaccess&utm_campaign=mutage&utm_medium=email

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