Meet our Council Members
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Professor David WalkerProfessor Paediatric Oncology
Children's Brain Tumour Research Centre
University of Nottingham
Nottingham NUH NHS Trust
B Med Sci BM BS FRCP FRCPCH
- Member SIOPEurope Board 2009-
- Member SIOPE Brain Tumour Committee (Representative for Training)
- Member Steering Group All Party Parliamentary Group for Brain and Spinal Tumours
- Co Chairman International Consortium of Low Grade Glioma
- Chair Brain Tumour Clinical Trials Committee UK Childrens Cancer Study Group (UKCCSG) 1990-1997
- Chair Societé Internationale d'Oncologie Pediatrique (SIOP) Brain Tumour Committee 1998-2000
- Clinical trials of novel therapies in brain and spinal tumours
- Health Services Research into Pathways to diagnosis of CNS tumours in childhood and adolescents
- Optimizing drug delivery to CNS tumours
- Low grade glioma of childhood
- Regional brain injury syndromes in childhood brain tumours
SIOPE Board Member
Avenue E.Mounier 83
Mr David Jellinek
- Consultant Neurosurgeon Royal Hallamshire Hospital Sheffield
- Honorary Senior Lecturer Neurosurgery University of Sheffield
|FRCS (Surg. Neurol.)||1994|
|Bachelor of Medical Science||1979|
Current research involves collaboration with the University of Sheffield in imaging brain tumours at 3Tesla to assess early predictive signs of malignant transformation of low grade glioma.
CLINICAL ACTIVITY AND CLINICAL RESEARCH
Neurosurgical Oncology: I am Lead clinician of the South Yorkshire Neuro Oncology MDT. I am chair of the DOH rare tumour group. I introduced 3 dimensional real time intraoperative brain scanning with high resolution ultrasound to the UK – a rapid a inexpensive practical alternative to intraoperative MRI scanning.
Wilkinson ID, Romanowski CA, Jellinek DA, Morris J, Griffiths PD
Motor functional MRI for pre-operative and intraoperative neurosurgical guidance.
Br J Radiol. 2003 Feb;76(902):98-103
Wharton SB, Hibberd S, Eward KL, Crimmins D, Jellinek DA, Levy D, Stoeber K, Williams GH.
DNA replication licensing and cell cycle kinetics of oligodendroglial tumours.
Br J Cancer. 2004 Jul 19;91(2):262-9.
Henson JD, Hannay JA, McCarthy SW, Royds JA, Yeager TR, Robinson RA, Wharton SB, Jellinek DA, Arbuckle SM, Yoo J, Robinson BG, Learoyd DL, Stalley PD, Bonar SF, Yu D, Pollock RE, Reddel RR.
A robust assay for alternative lengthening of telomeres in tumors shows the significance of alternative lengthening of telomeres in sarcomas and astrocytomas.
Clin Cancer Res. 2005 Jan 1;11(1):217-25
Chen YJ, Hakin-Smith V, Teo M, Xinarianos GE, Jellinek DA, Carroll T, McDowell D, MacFarlane MR, Boet R, Baguley BC, Braithwaite AW, Reddel RR, Royds JA.
Association of mutant TP53 with alternative lengthening of telomeres and favorable prognosis in glioma.
Cancer Res. 2006 Jul 1;66(13):6473-6
Wilkinson ID, Jellinek DA, Levy D, Giesel FL, Romanowski CA, Miller BA, Griffiths PD
Dexamethasone and enhancing solitary cerebral mass lesions: alterations in perfusion and blood-tumor barrier kinetics shown by magnetic resonance imaging.
Neurosurgery. 2006 Apr;58(4):640-6; discussion 640-6.
Dr Jeremy Rees
I am the Lead Clinician for Neuro-oncology at the National Hospital for Neurology and Neurosurgery where I have been a Consultant Neurologst since 1999. I also work at University College London Hospital, Royal Marsden Hospital, Mount Vernon Cancer Centre and Royal National Orthopaedic Hospital in Stanmore. I have a special interest and expertise in looking after patients with brain and spinal tumours particularly low-grade gliomas e.g. astrocytomas and oligodendrogliomas. I also see patients with cancer who have neurological problems such as neuropathy due to chemotherapy, radiotherapy side effects and paraneoplastic syndromes.
I qualified in 1988 from University College and Middlesex Medical School with distinctions in Medicine, Surgery and Therapeutics. After general professional training in various postgraduate London teaching hospitals, I was awarded a prestigious MRC Clinical Training Fellowship at Guy's Hospital, investigating the association between C jejuni infection and Guillain-Barre syndrome completing a PhD in 1985. I then did my neurology training at the Royal Free Hospital, National Hospital for Neurology and Neurosurgery, St Thomas' Hospital and neuro-oncology training at Memorial Sloan Kettering Cancer Center, New York.
I am the only neurologically trained neuro-oncologist in England, Ireland and Wales and am referred patients with neurological problems due to brain tumours or other cancers from all over the country and from abroad. I am a member of the National Cancer Research Network Brain Tumour Clinical Studies Group and worked with the Department of Health to draw up national guidelines for the referral of patients with suspected brain tumours.
I have extensive teaching experience both of medical students and qualified doctors, have given invited lectures at national and international neurology conferences and provided expert witness reports in medical negligence cases involving misdiagnosis and treatment of brain tumours.
I have published over fifty papers and reviews in scientific and medical journals, have contributed chapters on brain tumours and neurological complications of cancer to various reference books including the Oxford Textbook of Medicine and have recently edited a new book on neuro-oncology.
Professor Silvia Marino
Silvia Marino is Professor of Neuropathology at Barts and The London School of Medicine and Dentistry, Queen Mary University of London and also Honorary Consultant Neuropathologist at Barts and The London NHS Trust.
After studying Medicine at the University of Turin in Italy, Professor Marino trained in Neuropathology and Histopathology at the University of Zurich in Switzerland. She trained in molecular genetics with Professor Anton Berns at The Netherlands Cancer Institute in Amsterdam as a Marie Curie Postdoctoral Fellow of the European Community studying the role of the tumour suppressor Rb and p53 in the pathogenesis of medulloblastoma in genetically engineered mouse models.
She established her own laboratory research group in 2002 firstly at the Institute of Pathology, University of Zurich and then since 2006 at the Blizard Institute of Cell and Molecular Science in London, studying basic cellular and molecular mechanisms controlling the development of the central nervous system and how these mechanisms can contribute to developmental neuropathology and tumourigenesis when deregulated.
Professor Sebastian Brandner
Professor and Chair of Neuropathology
Division of Neuropathology and
Dept. of Neurodegenerative Disease
UCL Institute of Neurology
London WC1N 3BG
Clinical activity and diagnostic service :
The Department of Neuropathology at Queen Square is one of the leading academic and diagnostic neuropathology departments in the UK. The Department provides service for the National Hospital of Neurology and Neurosurgery, University College London Hospital, and receives a substantial number of national referrals.
The Department contributes to five weekly MDTs and carries out regular audits and a weekly case review forum.
Four honorary consultants and one locum consultant contribute to service and to research. Their involvement in research projects, leadership in clinical diagnostics and their research and publication activity is an indicator for the contribution of the Department of Neuropathology to the outstanding role of Queen Square in British clinical neurosciences.
We provide a comprehensive molecular diagnostic service for brain tumours. These tests help (i) improving our diagnoses and they are important to tell clinical oncologists how the patients may respond to chemotherapy.
We currently offer tests for the following gene mutations or chromosomal losses: 1p19q, EGFR amplification , EGFRvIII mutation, Chr 10q LOH )PTEN locus) and IDH-1/IDH-2 sequencing. We also routinely test all gliomas for MGMT promoter methylation.
The aim for 2010 is to test for the BRAF fusion gene in pilocytic astrocytomas (60-70% of PA are reported to have the fusion gene mutation). Although this has no direct prognostic implication, it will improve our diagnostic accuracy.
We provide these services to all patients operated on intrinsic brain tumours at the national Hospital and for referred cases from the UK and abroad.
Brain tumours and neural stem cells: Understanding the histogenesis and molecular pathogenesis of brain tumours. We are using transgenic mouse models to modify tumour suppressor genes in adult stem cells and trace the development of brain tumours.
We have recently established a mouse model for brain tumours, by inactivating tumour suppressor genes in the neural stem cell compartment. By injecting Cre-expressing virus into the ventricles of the mice the targeted genes are recombined only in cells located near the sub-ventricular zone (SVZ) which contains the glioma is induced in mice where PTEN and P53 or the trio of genes PTEN, P53 and Rb are targeted. We also have shown that in vitro recombined neural stem cells (i.e. neurospheres) of the same genotypes can be grown to tumour spheres in vitro and then grafted into the brain of a mouse. These grafts grow to brain tumours with an almost identical morphological phenotype compared those arising in vivo.
Development of a translational model for brain tumours: We will take these findings further and are currently translating them to human brain tumours. We will investigate whether human tumour-derived, cultured cells can be grafted into a mouse brain and yet mimic the primary human brain tumour. This system will enable us to study human tumour biology in a model very closely resembling the primary tumour. It will further allow us to test anti cancer therapies. It will further allow us to test anti cancer therapies. Ca 100 tumours are banked every year and from 30 tumours we establish cultures and cell lines.
|2006-2011||Role of Neural stem cells in CNS tumourigenesis
|2006-2009||PhD studentship (Alexander Swales); Role of Neural stem cells in CNS tumourigenesis
Brain Research Trust
|2006-2009||PhD studentship (Pedro Rodenas); Transgenic mouse model for aberrant Wnt signaling in the CNS
MRC capacity building studentship
|2006-2009||Wnt signalling in Neural stem cell differentiation and Tumourigenesis of the CNS
Samantha Dixon Research Trust
|2008-2011||Genomic and expression profiling of brain tumours Best research for Best health / UCLH comprehensive Biomedical Centre|
|2009-2010||High Field Imaging of a human glioma xenograft model, (BRT, Brain Tumour Fund)|
UCL Institute of Neurology; Division of Neuropathology:
MRC Neuromuscular Centre (UCL)
University College London Hospitals
- Jacques TS, Swales A, Brzozowski MJ, Henriquez NV, Linehan JM, Mirzadeh Z, O'Malley C, Naumann H, Alvarez-Buylla A, Brandner S. (2009): Combinations of genetic mutations in the adult neural stem cell compartment determine brain tumour phenotypes EMBO J. Nov 19. [Epub ahead of print]
- Robinson JP, Vanbrocklin MW, Guilbeault AR, Signorelli DL, Brandner S, Holmen SL (2009) Activated BRAF induces gliomas in mice when combined with Ink4a/Arf loss or Akt activation. Oncogene. Oct 26. [Epub ahead of print]
- Nayeem N, Kerr F, Naumann H, Linehan J, Lovestone S, and Brandner S (2007) Hyperphosphorylation of tau and neurofilaments and activation of CDK5 and ERK1/2 in PTEN-deficient cerebella. Mol Cell Neurosci, 34, 400-408.
- Wadsworth JD, Joiner S, Linehan JM, Cooper S, Powell C, Mallinson G, Buckell J, Gowland I, Asante EA, Budka H, Brandner S, and Collinge J (2006) Phenotypic heterogeneity in inherited prion disease (P102L) is associated with differential propagation of protease-resistant wild-type and mutant prion protein. Brain, 129, 1557-1569.
- Haegele L, Ingold B, Naumann H, Tabatabai G, Ledermann B, and Brandner S (2003) Wnt signalling inhibits neural differentiation of embryonic stem cells by controlling bone morphogenetic protein expression. Mol Cell Neurosci, 24, 696-708.
Prof. Dr. Clemens Oliver Hanemann, M.D.,Ph.D., FRCP
Current position: Chair in clinical neurology Peninusla Medical School
Consultant neurologist and academic lead department of neurology PHNT
Lead Neurologist, Peninsula Neuro oncology network
|Sept 2006||Board exam Medical Genetics|
|Nov 1998||Habilitation for Neurobiology and Neurology|
|Jan 1996||Board exam Neurology|
|Jan 1984 - Feb 1985||
Thesis (MD/PhD), Inst. of Molecular Neurobiology, University of Hamburg
|Oct 1981 - May 1988||
Medical school, University of Hamburg, (Würzburg, Glasgow, Johns Hopkins, Harvard)
|March 2010 - Nov 2010||
Assistant medical director R&D Plymouth Hospital NHS Trust
|March 2009 - March 2010||Deputy director R&D Plymouth Hospital NHS Trust|
|Since January 2000||
Assistant Professor, PI (Neurobiology/Neurology) University Ulm Neurology consultant
|1998||Assistant Professor (Neurobiology /Neurology), Dep. Neurology, Düsseldorf|
|Sept 1996||Neurology fellow, Department of Neurology, University of Düsseldorf|
|Sept 1990 - Sept 1996||Neurology resident, Department of Neurology, University of Düsseldorf|
Dep. Paediatric Neurology University of Michigan, Ann Arbor, USA
|February - March 1996||Lab. Neuromorphology, Department of Neurology, University Nijmegen|
|Sept 1988 - Sept 1990||
DFG research fellowship: at the Molecular Neurobiol. Lab, Dep. Neurology, University of Düsseldorf
Peer review experience
• Reviewer for the following journals:
J Neuroscience Methods; Neuropediatrics; Neuroscience Letters; PLOS Biology; Journal of Neurology, Neurosurgery and Psychiatry; Brain, Annals of Neurology, Neurogenetics, Biomed Central, Int J Cancer, Human Mutation, Brain Pathology, Neurobiology of disease, Genes, Chromosomes and Cancer, Human Molecular Genetics, Cancer Res, Oncogene, J Med Gen
• Ad hoc (frequently multiple times) reviewer for the following funding bodies:
Telethon, University Leiden, Bavarian government, Wellcome Trust, Prinses Beatrix Foundation, Childrens Tumour Foundation, Brain Tumour UK, Wales Office of Research and Development for Health and Social Care (WORD) Research Funding Scheme, Lord Dowding Fund, Deutsche Forschungsgemeinschaft (DFG)
• Member of funding committees:
Childrens Tumour Foundation
Lord Dowding Fund
• Member of other committees:
Member of the council British Neuro Oncology Society (since October 2010)
Translational subgroup NCRI brain tumour CSG
NCRI brain tumour CSG (since October 2010)
DeNDRoN MND GSG
Peninsula Medical School research committee (until November 2010)
Other external recognition
DFG scholarship at the laboratory for molecular Neurobiology, Dep. Neurology, Univ. Düsseldorf, 9/88-9/90
Bennigsen-Foerder award from the state NRW (highest scientific award from the state of NRW)
Previously consultant for Nexgenix pharamaceuticals
Invited to Novartis advisory board on Neurofibromatosis
Recent research grants
RDA PHD studentship, 1/06-1/09, £60808
Northcott Devon Medical Foundation, Verbrauchsmittel, £ 5000
RDA PhD studentship, 10/06-9/09, £61088
ChildrensTumour foundation, Drug Discovery award (2008), 11000$
ChildrensTumour foundation, Drug Discovery award (2009), 11000$
Dr Hadwen Trust (2008) 3 years covering a postdoctoral fellow and consumables, £130065
RDA PhD studentship with Dr Parkinson, £ 60000
PMS internal PhD studentship with Dr Caroll £ 39000
Deafness Research UK (2009) PhD studentship, £ 39349
PI, co-applicant in MND/DeNDRoN multi centre trial (LiCALS) to test Lithium in ALS, MNDA, £394.000
Novartis research fund (2010) £80.000
Hammer Out Brain tumour charity (2010) PhD studentship £36000
Supervisor of 14 Ph.D. and M.D. students (past and present)
Invited talks: 35
Selected papers (peer reviewed)
Sum citationen: 2457, h-index:22
Spreyer, G. Kuhn, C.O. Hanemann, C. P. Gillen, R. Kuhn, G. Lemke, H.W. Müller, (1991) Axon regulated expression of a Schwann cell mRNA homologous to a growth arrest specific gene, EMBO Journal 10 (12) 3661-3668
Timmerman V., Nelis E, Van Hul W. Nieuwenhuijsen B.W., Chen K.L., Ben Othman K., Cullen B., Leachz R.J., Hanemann C.O., Dejonghe P., Raymakers P., van Ommen G.-J.B., Martin J.J., Müller H.W., Vance J.M., Fischbeck K.H. and Van Broeckhoven C. (1992), The peripheral myelin protein gene pmp22 is Contained within the Charcot-Marie-Tooth disease type 1A duplication, Nature Genetics 1 171-175
Matsunami N., Smith B., Ballard L., Lensch M.W., Robertson M., Albertson H., Hanemann C.O., Müller H.W., et al. (1992), Peripheral myelin protein-22 gene maps in the duplication in chromosome 17 p11.2 associated with Charcot-Marie-Tooth 1A, Nature Genetics 1 176-179
CO Hanemann, Müller HW (1998). Pathogenesis of CMT1A neuropathy, Trends in Neuroscience 21: 282-286
CO Hanemann, Gabreëls-Festen AAWM, Stoll G, Müller HW (1996) Low affinity NGFR expression in CMT1A nerve biopsies. Brain 119: 1461-1469
CO Hanemann, D D´Urso, AAWM Gabreels:Festen, HW Müller (2000). Altered distribution of PMP22 in nerve biopsies from CMT1A patients with different PMP22 mutations, Brain 123:1001-6
Schulze K, Hanemann CO*, et al. (2002) Transduction of wt-merlin into human schwannomma cells decreases schwannoma cell growth and induces apoptosis. Human Molecular Genetics 11 (1) 69-76 *Corresponding author
Sperfeld AD, Hein C, Schröder JM, Ludolph AC Hanemann CO (2002) Occurrence and characterisation of peripheral nerve involvement in Neurofibromatosis Type 2 Brain 125:996-1004
Kämpchen K, Mielke K, Utermark T, Langmesser S, Hanemann CO (2003) Upregulation of the Rac1/JNK signalling pathway in primary human schwannoma cells, Human Molecular Genetics 12 (11): 1211-1221
Hirokawa J, Tikoo A, Huynh J, Utermark T, Hanemann CO, Giovannini M, Xiao GH, Testa JR, Wood J, Maruta H (2004). A clue to the therapy of neurofibromatosis type 2: NF2/Merlin is a PAK1 inhibitor. Cancer Journal 10 (1): 20-6
Utermark T, Kämpchen K, Haneman CO (2005). Reduced apotosis in Schwannomas, Brain Pathology, 15 (1): 17-22
Hanemann CO, Kämpchen K, Kaufmann D, Krause BJ. (2005) FDG PET CT of a giant retroperitoneal Schwannoma occurring in an NF2 patient, Arch Neurology, 62: 674-5.
Utermark T, Schubert SJA, Hanemann CO. (2005) Rearrangements of the intermediate filament GFAP in primary human schwannoma cells, Neurobiol Dis, 19:1-9
Grönholm M, Muranen T, Hanemann CO, Utermark T, Carpen O,.2006 Merlin interacts with the cell cycle regulator Hei10, Oncogene, 25:4389-98
Hirokawa Y, Nakajima H, Hanemann CO, Kurtz A, Frahm S, Mautner V, Maruta H (2005) Signal therapy of NF1-deficient tumor xenograft in mice by anti-PAK1 drug FK228, Cancer Biology and Therapy 4(4): 379-381
Hanemann CO, Bartelt-Kirbach B, Diebold R, Kämpchen K, Langmesser S, Utermark T (2006). Differential gene expression between human Schwannoma and control Schwann cells, J Neuropath Apl Neurobiol, 32:605-14
Hanemann CO, Evans DG (2006). News on the genetics, epidemiology, medical care and translational research of Schwannomas invited review J Neurol 253: 1533-41
Flaiz C, Kämpchen K, Matthies C; Hanermann CO (2007). Actin rich protrusions and non-localised GTPase activation in merlin deficient schwannomas, JNEN, 66:608-616
Hanemann CO (2008) Magic but treatable? Tumours due to loss of Merlin, Brain, 131:606-15
Ammoun S, Flaiz C, Ristic N, Hanemann CO (2008) Dissecting and targeting receptor-dependent and independent Erk pathway in human schwannoma, Cancer Research, 68:5236-5245
C. Flaiz, J Chernoff, S Ammoun, JR Peterson, CO Hanemann (2009). Regulation of Rac by PAK in schwannoma, Exp. Neurol, 218:137-144
M Widmer, CO Hanemann J Zajicek, (2008) High concentration s of cannabinoids activate apoptosis in human U373MG glioma cells,J. Neurosci. Res, 86(14):3212-20
C Flaiz, Utermark T, Parkinson D, Poetsch A, Hanemann CO (2008) Impaired intercellular adhesion and immature adherens junctions in merlin-deficient human primary schwannoma cells, Glia, 56:506-515
Christine Flaiz, Sylwia Ammoun , Anja Biebl , C Oliver Hanemann (2009) Altered adhesive structures and their relation to RhoGTPase activation in merlin-deficient schwannoma, Brain Pathology, 19:27-38
D Hilton N Ristic, CO Hanemann (2009) Activation of Erk, Akt and JNK signalling pathway in schwannomas in situ, Histopathology, 55:744-9
S Ammoun, D Hilton, C Matthies, CO Hanemann AZD62244 (2010), a MEK inhibitor, reduces Schwannoma proliferation,Neurobiol Dis, ;37(1):141-6.
S Ammoun CH. Cunliffe, JC. Allen, D Zagzag, CO Hanemann* and MA Karajannis (2010) EGF Receptor Family Activation and Lapatinib in Vestibular Schwannoma, Neurooncology, epub*corresponding author
Li W, You L, Cooper J, Schiavon G, Zhou L, Ishii R, Pepe-Caprio A, Giovannini M, Long SB, Erdjument-Bromage H, Hanneman CO, Zhou P, Tempst P & Giancotti F (2010). Merlin/NF2 Suppresses Tumorigenesis by Inhibiting the E3 Ubiquitin Ligase CRL4-DCAF1 in the Nucleus, Cell, 140:477-90
S Ammoun and CO Hanemann New Therapeutic Approaches for merlin deficient tumours, emerging molecular targets, Nature Reviews Neurology, invited
S Ammoun, MC Schmid, J Trainer and CO Hanemann, Evaluation of the efficiency of Imatinib and Nilotinib in the inhibition of PDGF-R- mediated ERK and AKT activation and proliferation of human schwannoma, in revision.
Professor Bob Lea is presently a Professor in Neurosciences, and Research Co-ordinator in the School of Pharmacy and Pharmaceutical Sciences, University of Central Lancashire.
His initial research concerned the neurobiology of endocrine/behaviour interactions. During this time he collaborated extensively with the Roslin Institute, Edinburgh, and research groups in North America, Europe and Japan.
Since 2003 his research interests shifted to clinical neuroscience and in particular the problem of brain tumour. In this respect he is co-founder of Brain Tumour North West, (2007), a strategic alliance of University and Health institutions throughout the North West of the UK. This enables the region to become a focus for co-ordinated, multi-disciplinary brain tumour research centred on the use of primary tissue.
Bob Lea has published over 100 peer reviewed articles in addition to a number of reviews and book chapters.
Dr Adam Waldman
BSc (Hons) MA PhD MBBChir MRCP FRCR
- Consultant Neuroradiologist and Honorary Clinical Reader, Imperial College, London
- Research Director, Imperial Hospitals Imaging Directorate
Royal College of Radiologists Roentgen Professor 2009
- Chair: National Cancer Research Network Brain Tumour Imaging Subgroup
- Member: National Cancer Research Network Brain Tumour Group
British Society of Neuroradiologists representative to BNOS
I originally studied basic sciences, and undertook a PhD and post-doctoral research in biophysics before training in medicine at Cambridge. My radiology and neuroradiology training was in London, and I have been a consultant since 2001. One of my main research interests is in basic and translational imaging development in neuro-oncology with particular reference to non-invasive tumour characterisation and improved imaging biomarkers for therapeutic development and clinical practice.
Dr Colin Watts
- HEFCE Senior Clinical Lecturer, Dept Clinical Neurosciences, Cambridge University
- Honorary Consultant Neurosurgeon Addenbrooke’s’ Hospital.
|FRCS (Surg. Neurol.)||2002|
|Bachelor of Medical Science||1990|
LABORATORY AND TRANSLATIONAL RESEARCH
My current research focuses on the similarities between brain cancer stem cells and endogenous adult stem cells. Building on our experience of handling human fetal and adult neural stem cells we have developed the Cambridge Protocol in which we have improved the efficiency of derivation of brain cancer stem cells to nearly 100% for high grade glioma. This has enabled us to begin to characterise these cells and compare them with normal glial progenitors. Using this approach I hope to be able to identify potential targets for further investigation and development leading to novel Phase I studies. I am also investigating the potential of these stem-like cells to predict and facilitate drug response in patients.
CLINICAL ACTIVITY AND CLINICAL RESEARCH
Neurosurgical Oncology: I am involved in the development of a brain tumour MDT approach and refinement of the pathway of care in accordance with NICE Cancer guidelines. This has also led to the development of a brain tumour outpatient clinic and counselling service in collaboration with clinical neuro-oncologists. The department has been proactive in recruiting patients to national studies including BR12 and the Cerepro trial and is seeking participation in further trials within the EORTC. Integration of clinical practice with ongoing research programmes has also led to increasing utilisation of surgical specimens including donations to our tumour tissue bank established by Prof Peter Collins. I am also the PI in a Phase 1 trial investigating the safety of using carmustine wafers in patients who have undergone fluorescence-guided tumour resections (GALA-5).
|GALA-5 Trial CRUK||2010 - 2012|
|Characterising Glioma Stem Cells ACT||2009 - 2010|
|Stem cells in the injured brain MRC G108/507||2003 - 2008|
|Fate mapping adult stem cells MRC stem cell initiative grant 67437 (with Prof J Fawcett)||2004 - 2007|
AWARDS AND APPOINTMENTS
|Committee member NCRI Clinical Trials Group, Brain Tumours||2008|
|Council Member British Neuro-Oncology Society (BNOS)||2008|
|Committee Member NCRI technology sub-group, Brain Tumours||2006 to date|
|HEFCE Senior Clinical Lecturer||2010 - 2015|
|MRC Clinician Scientist||2003 - 2008|
|MRC Clinical Training Fellowship||1996 - 1999|
Zhou JW, Raha-Chowhury R, Fawcett JW, Watts C Cytoplasmic Translocation/Nuclear Retention of Olig2 Mediates the Cell Fate Choice for NG2+Olig2+ Progenitors Following Acute Brain Injury. E.J.N. 2009 29; 1853-69.
Fael MT*, Ball SLR*, Zhou JW*, Fawcett JW*, Ichimura K, Collins P, Watts C*§ A system for efficient propagation of brain tumour stem cells. J. Neurosci Methods 2009 176; 192-199.
Clelland,C.D., Barker,R.A., Watts,C. Cell therapy in Huntington’s disease.
Neurosurg. Focus. 24, E9 (2008)
Joannides AJ, Webber DJ, Raineteau O, Kelly C, Irvine KA, Watts C, Rosser AE, Kemp PJ, Blakemore WF, Compston A, Caldwell MA, Allen ND, Chandran S.
Environmental signals regulate lineage choice and temporal maturation of neural stem cells from human embryonic stem cells.
Brain. 2007 May;130(Pt 5):1263-75.
Ozen I, Galichet C, Watts C, Parras C, Guillemot F, Raineteau O.
Proliferating neuronal progenitors in the postnatal hippocampus transiently express the proneural gene Ngn2.
Eur J Neurosci. 2007 25; 2591-2603.
Watts C, McConkey H, Anderson L, Caldwell M
Anatomical perspectives on adult stem cells. J Anat 207: 197-208; 2005
Rosser AE, Barker RA, Harrower T, Watts C, Farrington M, Ho AK, Burnstein RM, Menon DK, Gillard JH, Pickard JD, Dunnett SB, for the NEST-UK consortium.
Unilateral transplantation of human primary fetal tissue in four patients with Huntington’s disease: NEST-UK safety report ISRCTN no 26485475. J Neurol Neurosurg Psychiatry 73: 678-685; 2002
Eyre JA, Miller S, Clowrey GJ, Conway EA, Watts C
Functional corticospinal projections are established prenatally in the human foetus permitting involvement in the development of spinal motor centres. Brain 123: 51-64; 2000.
Maryanne’s career revolved around the Pharmaceutical Industry, at first, within several pharmaceutical companies where she was responsible for provision of medical information to healthcare professionals as well as clinical trial management.
After that she worked extensively in the sector which provides services to the Pharmaceutical Industry, notably marketing research, business intelligence and consultancy.
Latterly, she was Managing Director of a small company which facilitated benchmarking of sales, medical, marketing and research operations amongst UK and International pharmaceutical companies.
On leaving full time employment, Maryanne was for 6 years a Trustee for Brain Tumour UK, subsequently The Brain Tumour Charity, and has followed that by volunteering within the International Brain Tumour Alliance (IBTA) as well as for BNOS.
She is particularly interested in clinical research, pharmaceutical industry liaison, drug development, ensuring high quality, actionable statistical data, and marketing.