A novel imaging flow cytometry method for the detection of histone H4 acetylation in myeloid cells

Abstract

Background The histone deacetylase inhibitor (HDACI) valproic acid has been shown to inhibit the growth of multiple paediatric tumour types and is well tolerated in a childhood cancer setting. The current study was designed to develop a novel imaging flow cytometry method for the detection of histone H4 acetylation in white blood cells obtained from childhood cancer patients treated with valproic acid. Materials and methods HL‐60 cells and whole blood samples from healthy volunteers were incubated with valproic acid (0‐8 mM) for 0‐24 hours, with additional blood samples collected from ependymoma patients receiving valproic acid on the SIOP Ependymoma II clinical trial. An imaging flow cytometry method was developed using an ImageStream®χ flow cytometer, collecting 100 000 images per sample following excitation of PE tagged acH4 antibody and DAPI. Results The mean percentage of acH4‐positive cells increased to a greater extent than increases in mean and median fluorescence intensity following incubation with valproic acid. Comparable results were observed for in vitro and ex vivo experiments, and the assay was shown to be appropriate for clinical sample analysis. Myeloid cells exhibited a smaller proportion of acH4‐positive cells than the lymphoid population, but a greater fold increase above basal levels. Conclusions The percentage of acH4‐positive myeloid cells has the potential to be used as a robust pharmacodynamic biomarker for the measurement of acH4 for HDACIs. The developed assay is now being utilised in a clinical trial involving the treatment of childhood ependymoma patients with valproic acid.

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Current Methods of Post-Translational Modification Analysis and Their Applications in Blood Cancers

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