Staff Profile
Dr Rebecca Hill
Academic Clinical Lecturer
- Email: rebecca.hill@ncl.ac.uk
- Telephone: +44 (0) 191 208 2245
- Address: Wolfson Childhood Cancer Research Centre,
Northern Institute for Cancer Research,
Herschel Building, Level 6,
Newcastle University,
Newcastle upon Tyne,
NE1 7RU
Qualifications
PhD (Newcastle University Medical Sciences Doctoral Thesis Prize), Newcastle University, 2015
Certificate of Medical Education, Newcastle University, 2009
MRCPCH, Royal College of Paediatrics, 2006
MB BCh (with Commendation), University of Wales College of Medicine, 2003
Previous Positions
Mar 2015-present, NIHR Academic Clinical Lecturer, Northern Institute for Cancer Research
Sept 2014-Mar 2015, Paediatric Oncology National Grid Trainee, Newcastle upon Tyne NHS Trust
Mar 2010-Sept 2014, Clinical Research Associate, Northern Institute for Cancer Research
Sept 2008-Sept 2014, Paediatric Oncology Registrar, Newcastle upon Tyne NHS Trust
Mar 2007-Sept 2008, Paediatric Specialist Registrar, Northern Deanery
Aug 2006-Mar 2007, Paediatric Senior House Officer, Rhondda Cynon Taff NHS Trust
Aug 2004-Aug 2006, Paediatric Senior House Officer, Cardiff and Vale NHS Trust
Aug 2003-Aug2004, Pre-Registration House Officer, Swansea/Cardiff and Vale NHS Trust
Awards and Funding
Academy of Medical Sciences: Starter Grant
Action Medical Research Clinical: Research Fellowship
Cancer Research UK: Research Training Bursary
https://www.cancerresearchuk.org
European Society for Paediatric Oncology: Merit Award
ITCC: Society Ambassador, Methods in Clinical Cancer Research Workshop
https://www.ecco-org.eu/Events/MCCR-Workshop
JGW Patterson Foundation: Bridging Funding, Project Grant and Research Grant
http://jgwpattersonfoundation.co.uk
NECCR: Postgraduate Research Studentships
Newcastle University: Medical Sciences Doctoral Thesis Prize
https://www.ncl.ac.uk/fms/postgrad/awards/awards.htm
Professional Memberships
International Society for Paediatric Oncology Europe (SIOPE) - Young Oncologists Group
National Cancer Research Institute (NCRI) Clinical Studies Group - Brain Tumour Subgroup
Children’s Cancer and Leukaemia Group (CCLG) - Brain Tumour Special Interest Group
UK Embryonal Brain Tumour Group
British Medical Association
Royal College of Paediatrics and Child Health
The British Association for Cancer Research
European Association for Cancer Research
Research Interests
Medulloblastoma is the most common malignant brain tumour of childhood. Despite intensive, multimodal upfront-therapy (neurosurgery, radiotherapy and chemotherapy), relapse occurs in approximately 30% of patients and is almost universally fatal. Furthermore, relapse accounts for the majority of deaths in medulloblastoma, and a considerable, disproportionate amount of childhood cancer deaths overall.
In the past decade there has been an unprecedented expansion in our understanding of medulloblastoma at diagnosis, for example the discovery of the four consensus molecular subgroups (MBWNT, MBSHH, MBGroup3 and MBGroup4) and their translation into clinical trials and improved treatment stratification. Despite these discoveries in the disease at diagnosis, equivalent advances have yet to be made in the disease at relapse.
However, work undertaken by the Paediatric Brain Tumour Group, NICR, indicates that treatment selection pressure drives the evolution of therapy-resistance and disease recurrence in medulloblastoma. Parallel and convergent mechanisms of disease progression and treatment resistance are witnessed in a variety of cancer types, providing hope that these mechanisms are predictable and consequently therapeutically targetable. My particular area of research therefore focuses on understanding the evolving biology of medulloblastoma recurrence, aiming to identify anticipate and target these mechanisms to reduce relapse rates and improve disease survival.
- Izquierdo E, Yuan L, George S, Hubank M, Jones C, Proszek P, Shipley J, Gatz SA, Stinson C, Moore AS, Clifford SC, Hicks D, Lindsey JC, Hill RM, Jacques TS, Chalker J, Thway K, O'Connor S, Marshall L, Moreno L, Pearson A, Chesler L, Walker BA, De Castro DG. Development of a targeted sequencing approach to identify prognostic, predictive and diagnostic markers in paediatric solid tumours. Oncotarget 2017, 8(67), 112036-112050.
- Schwalbe EC, Lindsey JC, Nakjang S, Crosier S, Smith AJ, Hicks D, Rafiee G, Hill RM, Iliasova A, Stone T, Pizer B, Michalski A, Joshi A, Wharton SB, Jacques TS, Bailey S, Williamson D, Clifford SC. Novel molecular subgroups for clinical classification and outcome prediction in childhood medulloblastoma: a cohort study. The Lancet Oncology 2017, 18(7), 958-971.
- Lindsey JC, Hill RM, Schwalbe EC, Shrimpton ER, Howell CI, Rafiee G, Crosier S, Smith A, Ryan SL, Williamson D, Bailey S, Clifford SC. Molecular and Prognostic Heterogeneity within MYC and MYCN Amplified Medulloblastomas. In: International Symposium on Paediatric Neuro-Oncology (ISPNO). 2016, Liverpool, UK: Oxford University Press.
- Hicks D, Rafiee G, Schwalbe E, Howell C, Lindsey J, Hill R, Smith A, Crosier S, Joshi A, Robson K, Wharton S, Jacques T, Williamson D, Bailey S, Clifford S. Subgroup-Directed Stratification of Risk in Infant Medulloblastoma. In: 17th International Symposium on Pediatric Neuro-Oncology (ISPNO). 2016, Liverpool, UK: Oxford University Press.
- Williamson D, Lindsey JC, Hicks D, Crosier S, Smith A, Bashton M, Hill R, Joshi A, Jacques TS, Schwalbe EC, Bailey S, Clifford SC. The Transcriptional Landscape of Medulloblastoma: Group 3 and Group 4 Tumours Comprise a Single Clinically Significant Expression Continuum. In: 17th International Symposium on Pediatric Neuro-Oncology (ISPNO). 2016, Liverpool, UK: Oxford University Press.
- Hill RM, Kuijper S, Lindsey JC, Petrie K, Schwalbe EC, Barker K, Boult JKR, Williamson D, Ahmad Z, Hallsworth A, Ryan SL, Poon E, Robinson SP, Ruddle R, Raynaud FI, Howell L, Kwok C, Joshi A, Nicholson SL, Crosier S, Ellison DW, Wharton SB, Robson K, Michalski A, Hargrave D, Jacques TS, Pizer B, Bailey S, Swartling FJ, Weiss WA, Chesler L, Clifford SC. Combined MYC and P53 Defects Emerge at Medulloblastoma Relapse and Define Rapidly Progressive, Therapeutically Targetable Disease. Cancer Cell 2015, 27(1), 72-84.
- Hill R, Kuijper S, Lindsey J, Schwalbe E, Barker K, Boult J, Williamson D, Ahmad Z, Hallsworth A, Ryan S, Poon E, Robinson S, Ruddle R, Raynaud F, Howell L, Kwok C, Joshi A, Nicholson SL, Crosier S, Wharton S, Robson K, Michalski A, Hargrave D, Jacques T, Pizer B, Bailey S, Swartling F, Petrie K, Weiss W, Chesler L, Clifford S. MYC and TP53 defects emerge and interact at medulloblastoma relapse, define rapidly progressive disease and can be targeted therapeutically. In: 16th International Symposium on Pediatric Neuro-Oncology. 2014, Singapore: Oxford University Press.
- Hill RM, Kuijper S, Lindsey J, Schwalbe EC, Barker K, Boult J, Williamson D, Ahmad Z, Hallsworth A, Ryan S, Poon E, Robinson S, Ruddle R, Raynaud F, Howell L, Kwok C, Joshi A, Nicholson S, Crosier S, Wharton S, Jacques T, Robson K, Michalski A, Hargrave D, Pizer B, Bailey S, Swartling FJ, Petrie K, Weiss WA, Chesler L, Clifford S. MYC and TP53 defects interact at medulloblastoma relapse to define rapidly progressive disease and can be targeted therapeutically. In: AACR Annual Meeting. 2014, San Diego, CA, USA: American Association for Cancer Research.
- Schwalbe EC, Hayden JT, Rogers HA, Miller S, Lindsey JC, Hill RM, Nicholson SL, Kilday JP, Adamowicz-Brice M, Storer L, Jacques TS, Robson K, Lowe J, Williamson D, Grundy RG, Bailey S, Clifford SC. Histologically defined central nervous system primitive neuro-ectodermal tumours (CNS-PNETs) display heterogeneous DNA methylation profiles and show relationships to other paediatric brain tumour types. Acta Neuropathologica 2013, 126(6), 943-946.
- Zhukova N, Ramaswamy V, Remke M, Pfaff E, Shih DJ, Martin DC, Castelo-Branco P, Baskin B, Ray PN, Bouffet E, von-Bueren AO, Jones DT, Northcott PA, Kool M, Sturm D, Pugh TJ, Pomeroy SL, Cho YJ, Pietsch T, Gessi M, Rutkowski S, Bognar L, Klekner A, Cho BK, Kim SK, Wang KC, Eberhart CG, Fevre-Montange M, Fouladi M, French PJ, Kros M, Grajkowska WA, Gupta N, Weiss WA, Hauser P, Jabado N, Jouvet A, Jung S, Kumabe T, Lach B, Leonard JR, Rubin JB, Liau LM, Massimi L, Pollack IF, Shin-Ra Y, Van-Meir EG, Zitterbart K, Schüller U, Hill RM, Lindsey JC, Schwalbe EC, Bailey S, Ellison DW, Hawkins C, Malkin D, Clifford SC, Korshunov A, Pfister S, Taylor MD, Tabori U. Subgroup-Specific Prognostic Implications of TP53 Mutation in Medulloblastoma. Journal of Clinical Oncology 2013, 31(23), 2927-2935.
- Lindsey JC, Hill RM, Megahed H, Lusher ME, Schwalbe EC, Cole M, Hogg TL, Gilbertson RJ, Ellison DW, Bailey S, Clifford SC. TP53 Mutations in Favorable-Risk Wnt/Wingless-Subtype Medulloblastomas. Journal of Clinical Oncology 2011, 29(12), E344-E346.