School of Pharmacy
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I joined the School of Pharmacy in 2008. Following a PhD and post-doctoral work in pharmacology at Cambridge, I completed my post-doctoral training at the University of Virginia, USA. Following several years leading drug discovery programs in industry (Johnson & Johnson, Belgium and OSI pharmaceuticals, Oxford) I returned to academic research at the Institute of Cancer Research in London. At Keele, I lead teaching of pharmacology including option topics focusing on oncology molecular therapeutics. I also make teaching contributions to the School of Life Sciences and the School of Medicine. I am currently third year tutor. My research interests focus on discovering new therapeutic targets and drugs for the treatment of ovarian cancer. I have received funding from charities and research councils.
Research
- For details of my research into the treatment of ovarian cancer, please visit my laboratory web page: http://www.keele.ac.uk/istm/staff/richardsonalan/
Education
- Together with Luke Bracegirdle, I have developed "KUiz" a tool to allow academic staff to create rapidly a quiz for students that can be viewed on a smartphone or PC. For details please visit http://www.kuiz.co.uk/
- I use the Keele KAVE to teach molecular pharmacology in a 3D virtual environment, and I have shown that this improves student learning (in press, American Journal of Pharmacy Education).
- I have led the development of a synoptic assessment that allows students to integrate and entire year's learning (manuscript in preparation).
- I have developed an inexpensive method for simulating drug-receptor interactions in a classroom (manuscript submitted for publication).
Selected Publications
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2012. Autotaxin - a target for the treatment of drug-resistant ovarian cancer?. In Ovarian cancer - basic science perspective. Farghaly S (Ed.). (vol. 1). Intech. link>
Full Publications List show
Journal Articles
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2013. Preclinical Evaluation of Statins as a Treatment for Ovarian Cancer. Gynecologic Oncology, vol. 129, 417-424. doi>
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2008. Pharmacological inhibition of the Bcl-2 family of apoptosis regulators as cancer therapy. Curr Mol Pharmacol, vol. 1(3), 244-254. link>
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2008. Transient ectopic expression as a method to detect genes conferring drug resistance. International Journal of Cancer, vol. 122, 2641-2645. doi>
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2007. The Bcl-2/Bcl-XL Family Inhibitor ABT-737 Sensitizes Ovarian Cancer Cells to Carboplatin. Clinical Cancer Research, vol. 13, 7198. doi>
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2001. Serine phosphorylation of focal adhesion kinase in interphase and mitosis: A possible role in modulating binding to p130(Cas). MOLECULAR BIOLOGY OF THE CELL, vol. 12(1), 1-12. link>
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1998. Modular domains of focal adhesion-associated proteins. PROTEIN MODULES IN SIGNAL TRANSDUCTION, vol. 228, 135-163. link>
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1997. Inhibition of cell spreading by expression of the C-terminal domain of focal adhesion kinase (FAK) is rescued by coexpression of Src or catalytically inactive FAK: A role for paxillin tyrosine phosphorylation. MOLECULAR AND CELLULAR BIOLOGY, vol. 17(12), 6906-6914. link>
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1997. Identification of integrin-stimulated sites of serine phosphorylation in FRNK, the separately expressed C-terminal domain of focal adhesion kinase: A potential role for protein kinase A. BIOCHEMICAL JOURNAL, vol. 324, 141-149. link>
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1996. The identification of p130(cas)-binding proteins and their role in cellular transformation. ONCOGENE, vol. 12(11), 2467-2472. link>
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1996. Focal adhesion-associated kinases and cell signalling. JOURNAL OF NEUROCHEMISTRY, vol. 66, S7. link>
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1993. EFFECTS OF CA2+ CHELATORS ON PURIFIED INOSITOL 1,4,5-TRISPHOSPHATE (INSP3) RECEPTORS AND INSP3-STIMULATED CA2+ MOBILIZATION. JOURNAL OF BIOLOGICAL CHEMISTRY, vol. 268(16), 11528-11533. link>
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1992. PROLONGED EXPOSURE TO INOSITOL 1,4,5-TRISPHOSPHATE DOES NOT CAUSE INTRINSIC DESENSITIZATION OF THE INTRACELLULAR CA2+-MOBILIZING RECEPTOR. JOURNAL OF BIOLOGICAL CHEMISTRY, vol. 267(23), 16312-16316. link>
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1991. STRUCTURE AND FUNCTION OF INOSITOL TRISPHOSPHATE RECEPTORS. PHARMACOLOGY & THERAPEUTICS, vol. 51(1), 97-137. link>
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1994. FOCAL ADHESION KINASE - STRUCTURE AND SIGNALING. JOURNAL OF CELL SCIENCE, 109-113. link>
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Guanine nucleotide-binding protein-coupled and -uncoupled states of opioid receptors and their relevance to the determination of subtypes. Proceedings of the National Academy of Sciences of USA, vol. 89(21), 10198-10202. link>
Chapters
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2012. Autotaxin - a target for the treatment of drug-resistant ovarian cancer?. In Ovarian cancer - basic science perspective. Farghaly S (Ed.). (vol. 1). Intech. link>

