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Not applicable No embargo required No No embargo required No Embargo Required Cotter, Thomas G. Stanicka, Joanna Irish Cancer Society 2015-11-24T09:36:13Z 2015-11-24T09:36:13Z 2014 2014 Internal tandem duplication of FMS-like receptor tyrosine kinase (FLT3-ITD) has been associated with an aggressive AML phenotype. FLT3-ITD expressing cell lines have been shown to generate increased levels of reactive oxygen species (ROS) and DNA double strand breaks (dsbs). However, the molecular basis of how FLT3-ITD-driven ROS leads to the aggressive form of AML is not clearly understood. Herein, we observe that the majority of H2O2 in FLT3-ITD-expressing MV4-11 cells colocalises to the endoplasmic reticulum (ER). Furthermore, ER localisation of ROS in MV4-11 cells corresponds to the localisation of p22phox, a small membrane-bound subunit of NOX complex. Furthermore, we show that 32D cells, a myeloblast-like cell line transfected with FLT3-ITD, possess higher steady protein levels of p22phox than their wild type FLT3 (FLT3-WT)-expressing counterparts. Moreover, the inhibition of FLT3-ITD, using various FLT3 tyrosine kinase inhibitors, uniformly results in a posttranslational downregulation of p22phox. We also show that depletion of NOX2 and NOX4 and p22phox, but not NOX1 proteins causes a reduction in endogenous H2O2 levels. We show that genomic instability induced by FLT3-ITD leads to an increase in nuclear levels of H2O2. The presence of H2O2 in the nucleus is largely reduced by inhibition of FLT3-ITD or NOX. Furthermore, similar results are also observed following siRNA knockdowns of p22phox or NOX4. We demonstrate that 32D cells transfected with FLT3-ITD have a higher level of DNA damage than 32D cells transfected with FLT3-WT. Additionally, inhibition of FLT3-ITD, p22phox and NOX knockdowns decrease the number of DNA dsbs. In summary, this study presents a novel mechanism of genomic instability generation in FLT3-ITD-expressing AML cells, whereby FLT3-ITD activates NOX complexes by stabilising p22phox. This in turn leads to elevated generation of ROS and DNA damage in these cells. Irish Cancer Society (Research Scholarship Award CRS11STA) Not peer reviewed Accepted Version application/pdf Stanicka, J. 2014. Redox biology of myeloid leukaemias. PhD Thesis, University College Cork. 214 https://hdl.handle.net/10468/2088 en University College Cork © 2014, Joanna Stanicka. http://creativecommons.org/licenses/by-nc-nd/3.0/ Redox NADPH oxidase Leukaemia ROS FLT3 Genomic instability false Redox biology of myeloid leukaemias Doctoral thesis Doctoral PhD (Science) t.cotter@ucc.ieinfo:eu-repo/semantics/openAccess