Inhibiting the system x((C)over-bar)/glutathione axis selectively targets cancers with mutant-p53 accumulation
Web of Science
AuthorLiu, DS; Duong, CP; Haupt, S; Montgomery, KG; House, CM; Azar, WJ; Pearson, HB; Fisher, OM; Read, M; Guerra, GR; ...
Source TitleNature Communications
PublisherNATURE PUBLISHING GROUP
University of Melbourne Author/sClemons, Nicholas; Duong, Cuong; Guerra, Glen Robert; Haupt, Ygal; Phillips, Wayne; Cullinane, Carleen; Haupt, Susan; Liu, David; PEARSON, HELEN; Read, Matthew; ...
AffiliationSir Peter MacCallum Department of Oncology
Surgery (St Vincent's)
Document TypeJournal Article
CitationsLiu, D. S., Duong, C. P., Haupt, S., Montgomery, K. G., House, C. M., Azar, W. J., Pearson, H. B., Fisher, O. M., Read, M., Guerra, G. R., Haupt, Y., Cullinane, C., Wiman, K. G., Abrahmsen, L., Phillips, W. A. & Clemons, N. J. (2017). Inhibiting the system x((C)over-bar)/glutathione axis selectively targets cancers with mutant-p53 accumulation. NATURE COMMUNICATIONS, 8 (1), https://doi.org/10.1038/ncomms14844.
Access StatusOpen Access
NHMRC Grant codeNHMRC/1120293
TP53, a critical tumour suppressor gene, is mutated in over half of all cancers resulting in mutant-p53 protein accumulation and poor patient survival. Therapeutic strategies to target mutant-p53 cancers are urgently needed. We show that accumulated mutant-p53 protein suppresses the expression of SLC7A11, a component of the cystine/glutamate antiporter, system xC-, through binding to the master antioxidant transcription factor NRF2. This diminishes glutathione synthesis, rendering mutant-p53 tumours susceptible to oxidative damage. System xC- inhibitors specifically exploit this vulnerability to preferentially kill cancer cells with stabilized mutant-p53 protein. Moreover, we demonstrate that SLC7A11 expression is a novel and robust predictive biomarker for APR-246, a first-in-class mutant-p53 reactivator that also binds and depletes glutathione in tumours, triggering lipid peroxidative cell death. Importantly, system xC- antagonism strongly synergizes with APR-246 to induce apoptosis in mutant-p53 tumours. We propose a new paradigm for targeting cancers that accumulate mutant-p53 protein by inhibiting the SLC7A11-glutathione axis.
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