Sir Peter Ratcliffe grew up in north Lancashire and won an open scholarship to study medicine at Gonville and Caius College, Cambridge. He undertook clinical training at St. Bartholomew’s Hospital, London, and after series of posts at the London postgraduate hospitals, moved to Oxford to train in nephrology. In 1990 he obtained a Wellcome Trust Senior Fellowship to work on cellular responses to hypoxia, retrained in molecular biology and founded a new laboratory working on hypoxia biology in cancer and circulatory diseases. He was appointed Nuffield Professor and Head of the Nuffield Department of Clinical Medicine in 2003, a position he held until 2016. He is currently Director of the Target Discovery Institute, and a Member of the Ludwig Institute for Cancer Research. He is a Fellow of the Royal Society and the Academy of Medical Sciences and is an honorary member of the American Academy of Arts and Sciences. In the 2014 New Year’s Honours List, he was knighted for services to clinical medicine.
Professor Ratcliffe has led the hypoxia biology laboratory at Oxford for more than 20 years. The laboratory discovered the widespread operation of a system of direct oxygen sensing that is conserved throughout the animal kingdom and operates through a novel form of cell signalling involving post-translational hydroxylation of specific amino acids. Catalysis of these hydroxylations requires molecular oxygen and this generates the oxygen-sensitive signal. The laboratory now works extensively with Professor Chris Schofield in Chemistry to define the extent of biological operation and the therapeutic tractability of drug-based manipulation of the system in human disease.
Key Previous Publications
- The tumour suppressor protein VHL targets hypoxia-inducible factors for oxygen-dependent proteolysis. P.H.Maxwell, M.S.Wiesener, G.-W.Chang, S.C.Clifford, E.C.Vaux, M.E.Cockman, C.C.Wykoff, C.W.Pugh, E.R.Maher, P.J.Ratcliffe. Nature 399 (1999) 271-275.
- Targeting of HIF-a to the von Hippel-Lindau ubiquitylation complex by O2-regulated prolyl hydroxylation. P.Jaakkola, D.R.Mole, Y.-M.Tian, M.I.Wilson, J.Gielbert, S.J.Gaskell, A.vonKriegsheim, H.F.Hebestreit, M.Mukherji, C.J.Schofield, P.H.Maxwell, C.W.Pugh, P.J.Ratcliffe. Science 292 (2001) 468-472.
- C. elegans EGL-9 and mammalian homologs define a family of dioxygenases that regulate HIF by prolyl hydroxylation. A.C.R.Epstein, J.M.Gleadle, L.A.McNeill, K.S.Hewitson, J.F.O’Rourke, D.R.Mole, M.Mukherji, E.Metzen, M.I.Wilson, A.Dhanda, Y.-M.Tian, N.Masson, D.L.Hamilton, P.Jaakkola, R.Barstead, J.Hodgkin, P.H.Maxwell, C.W.Pugh, C.J.Schofield, P.J.Ratcliffe. Cell 107 (2001) 43-54
Selected Recent publications
- The FIH hydroxylase is a cellular peroxide sensor that modulates HIF transcriptional activity. Masson N, Singleton RS, Sekirnik R, Trudgian DC, Ambrose LJ, Miranda MX, Tian YM, Kessler BM, Schofield CJ, Ratcliffe PJ. EMBO Rep. 13 (2012) 251-7.
- Common genetic variants at the 11q13.3 renal cancer susceptibility locus influence binding of HIF to an enhancer of cyclin D1expression. Schödel J, Bardella C, Sciesielski L, Brown JM, Pugh CW, Buckle V, Tomlinson IP, Ratcliffe PJ, Mole DR. Nature Genetics 44 (2012) 420-5.
- Renal cyst formation in Fh1-deficient mice is independent of the Hif/Phd pathway: roles for fumarate in KEAP1 succination and Nrf2 signaling. Adam J, Hatipoglu E, O’Flaherty L, Ternette N, Sahgal N, Lockstone H, Baban D, Nye E, Stamp GW, Wolhuter K, Stevens M, Fischer R, Carmeliet P, Maxwell PH, Pugh CW, Frizzell N, Soga T, Kessler BM, El-Bahrawy M, Ratcliffe PJ, Pollard PJ. Cancer Cell. 20 (2011) 524-37.
- Proteomics-based identification of novel factor inhibiting HIF (FIH) substrates indicates widespread asparaginyl hydroxylation of ankyrin repeat domain-containing proteins. M.E.Cockman, J.D.Webb, H.B.Kramer, B.M.Kessler, P.J.Ratcliffe. Molecular & Cellular Proteomics 8 (2009) 535-546.
- Heterozygous deficiency of PHD2 restores tumor oxygenation and inhibits metastasis via endothelial normalization. M.Mazzone, D.Dettori, R.L.deOliveira, S.Loges, T.Schmidt, B.Jonckx, Y.-M.Tian, A.A.Lanahan, P.Pollard, C.R.deAlmodovar, F.DeSmet, S.Vinckier, J.Aragones, K.Debackere, A.Luttun, S.Wyns, B.Jordan, A.Pisacane, B.Gallez, M.G.Lampugnani, E.Dejana, M.Simons, P.Ratcliffe, P.Maxwell, P.Carmeliet. Cell 136 (2009) 839-851.