Advanced Cancer Models and Therapeutics Group
Developing novel Immunotherapeutic approaches to cancer using advanced physiological disease models and spatial biological approaches.
Utilising our cross-disciplinary team spanning cancer biologists, surgeon-scientists, engineers and spatial biologists, our group focusses on difficult to treat cancers. We achieve this through the development of human cancer model systems, cutting edge spatial biology and the development of novel therapeutics.
Cancer Model Systems (Gordon-Weeks/Fisher)
A perfect cancer model system is entirely human, incorporates the plethora of cell types found with tissues and includes a physiological route for drug delivery. Current systems fail on one and sometimes all of these parameters and failure to develop systems that faithfully recapitulate human cancer biology now provides a bottle neck to successful therapeutic design. Our model systems range from organ-on-chip microfluidic systems, through tissue avatars all the way to whole organ perfusion platforms enabling delivery of therapeutics coupled with pre- and post-treatment tissue analysis. We will use these systems to uncover mechanisms of inherent immune evasion, therapeutic resistance, to de-risk clinical trials and reduced animal experimentation in cancer research.
Spatial Biology (Gordon-Weeks)
The coupling of AI and advanced imaging techniques is leading to a field change in the way we analyse cancer samples. Spatial biological approaches involve the mapping of multiple cell types across large areas of tissue such that topology and structure can be understood and utilised to describe biological phenomena. The recent addition of whole transcriptome, single cell spatial pipelines is enabling understanding of how the transcriptome of specific cell types changes based on tissue location and proximity with communicating cell types. We utilise these techniques to analyse archived cancer specimens and to interrogate the biological efficacy of therapeutics delivered to our cancer models. This is building a greater understanding of how the cancer manipulates its tissue of origin to evade immune destruction and support disease progression.
Therapeutic Development (Fisher/Seymour)
Principle Investigators
Lab Members
Key Publications
Colorectal cancer liver metastatic growth depends on PAD4-driven citrullination of the extracellular matrix.
Yuzhalin AE. et al, (2018), Nat Commun, 9
Phase 1 study of intravenous administration of the chimeric adenovirus enadenotucirev in patients undergoing primary tumor resection.
Garcia-Carbonero R. et al, (2017), J Immunother Cancer, 5
Preclinical Safety Studies of Enadenotucirev, a Chimeric Group B Human-Specific Oncolytic Adenovirus.
Illingworth S. et al, (2017), Mol Ther Oncolytics, 5, 62 - 74
Neutrophils promote hepatic metastasis growth through fibroblast growth factor 2-dependent angiogenesis in mice.
Gordon-Weeks AN. et al, (2017), Hepatology, 65, 1920 - 1935
FGF2 alters macrophage polarization, tumour immunity and growth and can be targeted during radiotherapy.
Im JH. et al, (2020), Nat Commun, 11
Latest publications
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T cell engagers: expanding horizons in oncology and beyond.
Journal article
Albayrak G. et al, (2025), Br J Cancer
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Ex vivo model of functioning human lymph node reveals role for innate lymphocytes and stroma in response to vaccine adjuvant.
Journal article
Fergusson JR. et al, (2025), Cell Rep, 44
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Iatrogenic Subcapsular Haematoma Leads to 151% Growth of Future Liver Remnant.
Journal article
Fu H. et al, (2025), Cardiovasc Intervent Radiol
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Induction of macrophage efferocytosis in pancreatic cancer via PI3Kγ inhibition and radiotherapy promotes tumour control.
Journal article
Russell SN. et al, (2025), Gut, 74, 825 - 839
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A commentary on: “Effect of Preoperative Autologous Blood Storage in Major Hepatectomy for Perihilar Malignancy: A Randomized Controlled Trial”
Journal article
Lakha AS. and Gordon-Weeks A., (2025), AME Surgical Journal, 5
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Simultaneous versus delayed resection of synchronous colorectal liver metastases: A systematic review and meta-analysis.
Journal article
Lakha AS. et al, (2025), Eur J Surg Oncol, 51

