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Stephen Edward Hiscox
Researcher at Cardiff University
Publications - 85
Citations - 4849
Stephen Edward Hiscox is an academic researcher from Cardiff University. The author has contributed to research in topics: Breast cancer & Cancer. The author has an hindex of 38, co-authored 85 publications receiving 4584 citations. Previous affiliations of Stephen Edward Hiscox include University of Wales & AstraZeneca.
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Journal ArticleDOI
Critical research gaps and translational priorities for the successful prevention and treatment of breast cancer.
Suzanne A. Eccles,Eric O. Aboagye,Simak Ali,Annie S. Anderson,Jo Armes,Fedor Berditchevski,Jeremy P. Blaydes,Keith Brennan,Nicola J. Brown,Helen E. Bryant,Nigel J Bundred,Joy Burchell,Anna Campbell,Jason S. Carroll,Robert Clarke,Charlotte E. Coles,Gary Cook,Angela Cox,Nicola J. Curtin,Lodewijk V. Dekker,Isabel dos Santos Silva,Stephen W. Duffy,Douglas F. Easton,Diana Eccles,Dylan R. Edwards,Joanne Edwards,D. G. R. Evans,Deborah Fenlon,James M. Flanagan,Claire Foster,William M. Gallagher,Montserrat Garcia-Closas,Julia Margaret Wendy Gee,Andy J. Gescher,Vicky Goh,Ashley M. Groves,Amanda J. Harvey,Michelle Harvie,Bryan T. Hennessy,Stephen Edward Hiscox,Ingunn Holen,Sacha J Howell,Anthony Howell,Gill Hubbard,Nicholas J. Hulbert-Williams,Myra S. Hunter,Bharat Jasani,Louise J. Jones,Timothy J. Key,Cliona C. Kirwan,Anthony Kong,Ian Kunkler,Simon P. Langdon,Martin O. Leach,David J. Mann,John Marshall,Lesley Ann Martin,Stewart G. Martin,Jennifer E. Macdougall,David Miles,William R. Miller,Joanna R. Morris,Sue Moss,Paul B. Mullan,Rachel Natrajan,James P B O'Connor,Rosemary O'Connor,Carlo Palmieri,Paul D.P. Pharoah,Emad A. Rakha,Elizabeth Reed,Simon P. Robinson,Erik Sahai,John M. Saxton,Peter Schmid,Matthew J. Smalley,Valerie Speirs,Robert Stein,John Stingl,Charles H. Streuli,Andrew Tutt,Galina Velikova,Rosemary A. Walker,Christine J. Watson,Kaye J. Williams,Leonie S. Young,Alastair M. Thompson +86 more
TL;DR: With resources to conduct further high-quality targeted research focusing on the gaps identified, increased knowledge translating into improved clinical care should be achievable within five years.
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Insulin-like growth factor-I receptor signalling and acquired resistance to gefitinib (ZD1839; Iressa) in human breast and prostate cancer cells
Helen E. Jones,Lindy Goddard,Julia Margaret Wendy Gee,Stephen Edward Hiscox,Michele Rubini,Denise Barrow,Janice Mary Knowlden,Sophie E. Williams,A. E. Wakeling,Robert Ian Nicholson +9 more
TL;DR: It is concluded that in breast and prostate cancer cells acquired resistance to gefitinib is associated with increased signalling via the IGF-1R pathway, which also plays a role in the invasive capacity of the gefitsinib-resistant phenotype.
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Hepatocyte growth factor/scatter factor, its molecular, cellular and clinical implications in cancer.
TL;DR: The HGF/SF receptor and intracellular signalling, Ras, rho, raf and rac are involved in c-met cell signalling, and Stimulation of MAP kinase pathways.
Journal ArticleDOI
Tamoxifen resistance in MCF7 cells promotes EMT-like behaviour and involves modulation of beta-catenin phosphorylation.
Stephen Edward Hiscox,Wen Guo Jiang,Kathrin Obermeier,Kathryn Mary Taylor,Liam David Morgan,Rajpal Singh Burmi,Denise Barrow,Robert Ian Nicholson +7 more
TL;DR: Results suggest that homotypic adhesion in tamoxifen‐resistant breast cancer cells is dysfunctional due to EGFR‐driven modulation of the phosphorylation status of β‐catenin and may contribute to an enhanced aggressive phenotype and transition towards a mesenchymal phenotype in vitro.
Journal ArticleDOI
Elevated Src activity promotes cellular invasion and motility in tamoxifen resistant breast cancer cells.
Stephen Edward Hiscox,Liam David Morgan,Tim P. Green,Denise Barrow,Julia Margaret Wendy Gee,Robert Ian Nicholson +5 more
TL;DR: Observations suggest that Src plays a pivotal role in mediating the motile and invasive phenotype observed in endocrine-resistant breast cancer cells, and the use of Src inhibitors in conjunction with EGFR inhibitors such as gefitinib may provide an effective method with which to prevent cancer progression and metastasis.