Alison Banham
BA, MA, DPhil (Oxon), FRCPath
Emeritus Professor
The study of transcriptional de-regulation in B-cell malignancies and the development of novel antibodies for cancer therapy.
Alison Banham's academic qualifications include BA, MA and D.Phil. (PhD) degrees from the University of Oxford and Fellowship of the Royal College of Pathologists.
Professor Banham is a founder member and Vice President of the European Network of Monoclonal Antibody Producing Laboratories. She is internationally recognised for her expertise in the production and characterisation of monoclonal antibodies and has written guidelines to promote effective antibody validation. She has also made key contributions to the design and delivery of EuroMabNet workshops that teach young scientists how to validate antibodies.
Since 1995 Professor Banham's main research focus has been within the field of cancer, particularly aggressive B-cell malignancies, focussing initially on the identification and characterisation of novel diagnostic and prognostic biomarkers. These have included the FOXP family of forkhead transcription factors (FOXP1-4) and the cancer testis antigen PASD1. These de-regulated transcription factors have functional roles in tumour biology and strategies are being investigated to enable their future therapeutic targeting in diffuse large B-cell lymphoma and multiple myeloma.
Professor Banham's team are also generating novel therapeutic antibodies. These include antibodies targeting the tumour vasculature, in particular the Notch ligand Jagged-1 and the adhesion G-protein coupled receptor ELTD1. She is also pursuing the development of TCR mimic antibodies which recognise peptides from intracellular tumour proteins that are presented on the cell surface by MHC class I molecules. This enables targeting of the intracellular proteome and antibodies to the p53 oncosuppressor are being further characterised.
Key publications
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FOXP1 suppresses immune response signatures and MHC class II expression in activated B-cell-like diffuse large B-cell lymphomas.
Journal article
Brown PJ. et al, (2016), Leukemia, 30, 605 - 616
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The European antibody network's practical guide to finding and validating suitable antibodies for research.
Journal article
Roncador G. et al, (2016), MAbs, 8, 27 - 36
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A core human primary tumor angiogenesis signature identifies the endothelial orphan receptor ELTD1 as a key regulator of angiogenesis.
Journal article
Masiero M. et al, (2013), Cancer Cell, 24, 229 - 241
Recent publications
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Carbonic anhydrase 9 (CA9) expression in non-small-cell lung cancer: correlation with regulatory FOXP3+T-cell tumour stroma infiltration.
Journal article
Giatromanolaki A. et al, (2020), Br J Cancer
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CRISPR/Cas9-Mediated Foxp1 Silencing Restores Immune Surveillance in an Immunocompetent A20 Lymphoma Model.
Journal article
Felce SL. et al, (2020), Front Oncol, 10
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ADGRL4/ELTD1 Silencing in Endothelial Cells Induces ACLY and SLC25A1 and Alters the Cellular Metabolic Profile.
Journal article
Favara DM. et al, (2019), Metabolites, 9
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Development of therapeutic anti-JAGGED1 antibodies for cancer therapy.
Journal article
Masiero M. et al, (2019), Mol Cancer Ther
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ADGRL4/ELTD1 is a highly conserved angiogenesis-associated orphan adhesion GPCR that emerged with the first vertebrates and comprises 3 evolutionary variants.
Journal article
Favara DM. et al, (2019), BMC Evol Biol, 19
ORCID
0000-0002-3197-273X