Mr Matthew Fisher
BSc (Hons)
School of Medicine and Population Health
Technical Specialist – BSU
matthew.fisher@sheffield.ac.uk
+44 114 215 9067
+44 114 215 9067
GU36, The Medical School
Full contact details
Mr Matthew Fisher
School of Medicine and Population Health
GU36
The Medical School
Beech Hill Road
Sheffield
S10 2RX
School of Medicine and Population Health
GU36
The Medical School
Beech Hill Road
Sheffield
S10 2RX
- Research interests
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The TMG study the blood vessels that supply tumours with oxygen and nutrients and their role in cancer therapy. Tumours require a blood supply to grow and the blood vessels provide a route for the spread of tumour cells to other sites in the body. Therefore, targeting treatment to the blood vessels rather than the tumour cells is a potential means of killing tumours. Much of the research involves using vascular disrupting agents (VDAs) e.g. CA4P, and the susceptibility of tumour vessels to vascular shutdown.
- Publications
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Featured publications
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All publications
Journal articles
- Targeting a STING agonist to perivascular macrophages in prostate tumors delays resistance to androgen deprivation therapy. Journal for ImmunoTherapy of Cancer, 12(7). View this article in WRRO
- Sialic acid blockade inhibits the metastatic spread of prostate cancer to bone. eBioMedicine, 104. View this article in WRRO
- Rac1 controls cell turnover and reversibility of the involution process in postpartum mammary glands. PLoS Biology, 21(1).
- Cover feature : Evaluation of sydnone-based analogues of Combretastatin A-4 phosphate (CA4P) as vascular disrupting agents for use in cancer therapy (ChemMedChem 24/2018). ChemMedChem, 13(24), 2600-2600. View this article in WRRO
- Evaluation of sydnone-based analogs of combretastatin A-4 phosphate (CA4P) as vascular disrupting agents for use in cancer therapy. ChemMedChem, 13(24), 2618-2626. View this article in WRRO
- ARQ-197, a small-molecule inhibitor of c-Met, reduces tumour burden and prevents myeloma-induced bone disease in vivo. PLoS One, 13(6). View this article in WRRO
- Vascular patterning of subcutaneous mouse fibrosarcomas expressing individual VEGF isoforms can be differentiated using angiographic optical coherence tomography. Biomedical Optics Express, 8(10), 4551-4567. View this article in WRRO
- The protective role of sphingosine-1-phosphate against the action of the vascular disrupting agent combretastatin A-4 3-O-phosphate. Oncotarget, 2017(8), 95648-95661. View this article in WRRO
- Differential Expression of VEGFA Isoforms Regulates Metastasis and Response to Anti-VEGFA Therapy in Sarcoma. Cancer Research, 77(10). View this article in WRRO
- Sydnone Cycloaddition Route to Pyrazole-Based Analogs of Combretastatin A4.. Journal of Medicinal Chemistry, 59(20), 9473-9488. View this article in WRRO
- An in vivo role for Rho kinase activation in the tumour vascular disrupting activity of combretastatin A-4 3-O-phosphate. British Journal of Pharmacology, 171(21), 4902-4913. View this article in WRRO
- Influence of soluble or matrix-bound isoforms of vascular endothelial growth factor-A on tumor response to vascular-targeted strategies. International Journal of Cancer, n/a-n/a.
- Do Anti-Angiogenic VEGF (VEGFxxxb) Isoforms Exist? A Cautionary Tale. PLoS ONE, 7(5). View this article in WRRO
- Abstract 5296: The role of VEGF receptors 1 and 2 on tumor vascularization and progression in single VEGF isoform expressing tumors. Cancer Research, 72(8_Supplement), 5296-5296.
- Abstract 1371: Delineating the function of single VEGF isoforms using both proteomic and molecular approaches. Cancer Research, 72(8_Supplement), 1371-1371.
- Abstract 3279: Effects of the isoforms of the angiogenic growth factor VEGF on neo-vascularization and tumor response to the tyrosine kinase inhibitor cediranib. Cancer Research, 71(8_Supplement), 3279-3279.
- Abstract 2849: Tie2-expressing macrophages (TEM) depletion may enhance the clinical efficacy of combretastatin A-4-phosphate (CA-4-P). Cancer Research, 71(8_Supplement), 2849-2849.
- Vascular effects dominate solid tumor response to treatment with combretastatin A‐4‐phosphate. International Journal of Cancer, 129(8), 1979-1989.
- TIE2-expressing macrophages limit the therapeutic efficacy of the vascular-disrupting agent combretastatin A4 phosphate in mice. Journal of Clinical Investigation, 121(5), 1969-1973.
- Microflow of fluorescently labelled red blood cells in tumours expressing single isoforms of VEGF and their response to vascular targeting agents. Medical Engineering and Physics, 33(7), 805-809. View this article in WRRO
Conference proceedings papers
- Abstract A57: Differential tumor cell expression of VEGF isoforms impacts on the tumor microenvironment, metastasis and radiation response in a mouse fibrosarcoma model. Cancer Research, Vol. 75(1_Supplement) (pp A57-A57)
- Abstract 1578: A critical role for RhoA-GTPase signaling in the tumor vascular disrupting action of combretastatin-A4-phosphate in vivo. Cancer Research, Vol. 71(8_Supplement) (pp 1578-1578)
Preprints
- Targeting of a STING Agonist to Perivascular Macrophages in Prostate Tumors Delays Resistance to Androgen Deprivation Therapy, Cold Spring Harbor Laboratory.
- Rac1 controls cell turnover and mammary gland reversibility in post-partum involution, Cold Spring Harbor Laboratory.
- Targeting a STING agonist to perivascular macrophages in prostate tumors delays resistance to androgen deprivation therapy. Journal for ImmunoTherapy of Cancer, 12(7). View this article in WRRO