Journal article
Co-targeting bromodomain and extra-terminal proteins and MCL1 induces synergistic cell death in melanoma
HY Tseng, J Dreyer, AA Emran, D Gunatilake, M Pirozyan, C Cullinane, K Dutton-Regester, H Rizos, NK Hayward, G McArthur, P Hersey, J Tiffen, S Gallagher
International Journal of Cancer | WILEY | Published : 2020
DOI: 10.1002/ijc.33000
Abstract
The treatment of melanoma has been markedly improved by the introduction of targeted therapies and checkpoint blockade immunotherapy. Unfortunately, resistance to these therapies remains a limitation. Novel anticancer therapeutics targeting the MCL1 anti-apoptotic protein have shown impressive responses in haematological cancers but are yet to be evaluated in melanoma. To assess the sensitivity of melanoma to new MCL1 inhibitors, we measured the response of 51 melanoma cell lines to the novel MCL1 inhibitor, S63845. Additionally, we assessed combination of this drug with inhibitors of the bromodomain and extra-terminal (BET) protein family of epigenetic readers, which we postulated would ass..
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Awarded by National Health and Medical Research Council
Funding Acknowledgements
This work is supported by Cancer Council NSW Project Grant 18-05 and National Health and Medical Research Council Program Grant 1093017. The authors would like to thank the Sydney Cytometry Core Research Facility and Centenary Imaging Facility for their technical support.