Woodley, KeithDillingh, LSGiotopoulos, GeorgeMadrigal, PedroRattigan, KMPhilippe, CélineDembitz, VilmaMagee, AMSAsby, Rvan de Lagemaat, Louie NMapperley, ChristopherJames, SCPrehn, JHMTzelepis, KonstantinosRouault-Pierre, KevinVassiliou, GeorgeKranc, KamilHelgason, G VignirHuntly, BJPGallipoli, Paolo2023-09-142023-09-142023-04-14Woodley, K, Dillingh, LS, Giotopoulos, G, Madrigal, P, Rattigan, KM, Philippe, C, Dembitz, V, Magee, AMS, Asby, R, van de Lagemaat, L N, Mapperley, C, James, SC, Prehn, JHM, Tzelepis, K, Rouault-Pierre, K, Vassiliou, G, Kranc, K, Helgason, G V, Huntly, BJP & Gallipoli, P 2023, 'Mannose metabolism inhibition sensitizes acute myeloid leukaemia cells to therapy by driving ferroptotic cell death.', Nature Communications, vol. 14, 2132. https://doi.org/10.1038/s41467-023-37652-02041-1723ORCID: /0000-0002-2947-1557/work/140168203https://hdl.handle.net/2164/21669Acknowledgements We wish to thank the Barts Cancer Institute tissue bank for sample collection and processing. This research was supported by the BCI Flow cytometry facility (CRUK Core Award C16420/A18066). This work was supported by the Wellcome Trust (PG, 109967/Z/15/Z), the American Society of Haematology (PG, Global Research Award) and Cancer Research UK (PG, Advanced Clinician Scientist fellowship, C57799/A27964). K.R-P. was supported by the Academy of Medical Sciences (SBF004\1099) J.H.M.P. was supported by a research grant from Science Foundation Ireland (SFI) under Grant Number 16/RC/3948 and co-funded under the European Regional Development Fund and by FutureNeuro industry partners. K.T. was funded by Wellcome Trust (Grant References: RG94424, RG83195, G106133), UKRI Medical Research Council (RG83195) and Leukaemia UK (G108148).191565762engSDG 3 - Good Health and Well-beingcancer metabolismcancer therapeutic resistanceR MedicineWellcome TrustPG, 109967/Z/15/ZRG94424RG83195Cancer Research UKC16420/A18066C57799/A27964G106133Medical Research Council (MRC)RG83195Supplementary DataRMannose metabolism inhibition sensitizes acute myeloid leukaemia cells to therapy by driving ferroptotic cell death.Journal article10.1038/s41467-023-37652-0https://europepmc.org/articles/PMC1010486114