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Annette Hayden

University of Southampton - School of Cancer Sciences

Southampton

United Kingdom

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Scholarly Papers (1)

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Modulation of the Tumor Promoting Functions of Cancer Associated Fibroblasts by Phosphodiesterase Type 5 Inhibition Increases the Efficacy of Chemotherapy in Human Preclinical Models of Esophageal Adenocarcinoma

Number of pages: 95 Posted: 15 Sep 2021
Annette Hayden, Antigoni Manousopoulou, Benjamin P. Sharpe, Andrew Cowie, Robert C. Walker, Jack Harrington, Fereshteh Izadi, Fereshteh Izadi, Stella P. Breininger, Ewan Kyle, John H. Saunders, Simon L. Parsons, Simon L. Parsons, Alison A. Ritchie, Philip A. Clarke, Pamela Collier, Spiros D. Garbis, Zoë Walters, Matthew Rose-Zerilli, Anna M. Grabowska and Timothy J. Underwood
University of Southampton - School of Cancer Sciences, Proteas Bioanalytics Inc., University of Southampton - School of Cancer Sciences, University of Southampton - School of Cancer Sciences, University of Southampton - School of Cancer Sciences, University of Southampton - School of Cancer Sciences, Swansea University - Swansea University Medical SchoolUniversity of Southampton - School of Cancer Sciences, University of Southampton - School of Cancer Sciences, University of Southampton - School of Cancer Sciences, University of Nottingham - Ex Vivo Cancer Pharmacology Centre of Excellence, Nottingham University Hospitals NHS TrustUniversity of Nottingham - Ex Vivo Cancer Pharmacology Centre of Excellence, University of Nottingham - Ex Vivo Cancer Pharmacology Centre of Excellence, University of Nottingham - Ex Vivo Cancer Pharmacology Centre of Excellence, University of Nottingham - Ex Vivo Cancer Pharmacology Centre of Excellence, Proteas Bioanalytics Inc., University of Southampton - School of Cancer Sciences, University of Southampton - School of Cancer Sciences, University of Nottingham - Ex Vivo Cancer Pharmacology Centre of Excellence and University of Southampton - School of Cancer Sciences
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Abstract:

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esophageal adenocarcinoma, cancer associated fibroblasts, phosphodiesterase type 5 inhibitors, chemotherapy, preclinical models