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Oxygen sensing

Our laboratory is studying the role of hypoxia and related metabolic stresses in driving aggressive cancer phenotypes. A specific focus is on the role of transcriptional cascades mediated by hypoxia inducible factors (HIFs). These pathways are almost universally activated in cancer, both by micro-environmental hypoxia and by direct connections to oncogene and tumor suppressors.

We are interested in both hypoxia signalling pathways themselves, and in the general implications of activating very extensive interconnected signalling pathways during cancer development. A particular focus of our work is on understanding how multiple pro- and anti-tumorigenic effects of hypoxia pathway ‘switching’ are accommodated during cancer development, including how these processes drive tumour heterogeneity, chaotic cancer cell biology, and resistance to treatment.

Our team

Selected publications

OGFOD1 catalyzes prolyl hydroxylation of RPS23 and is involved in translation control and stress granule formation

Journal article

Singleton RS. et al, (2014), Proceedings of the National Academy of Sciences, 111, 4031 - 4036

The FIH hydroxylase is a cellular peroxide sensor that modulates HIF transcriptional activity

Journal article

Masson N. et al, (2012), EMBO reports, 13, 251 - 257

High-resolution genome-wide mapping of HIF-binding sites by ChIP-seq

Journal article

Schödel J. et al, (2011), Blood, 117, e207 - e217