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Improving radiotherapy via novel drug-radiation interactions

Project fact file

Professor Stewart Martin
School / Division
Division of Cancer and Stem Cells
Radiation biology; Combined therapies; Biomarkers; Drug interactions; Radiotherapy; Breast cancer; Pancreatic cancer
Fee band
Lab-based research
Date posted
November 2017

Project description

There is an urgent need to develop new therapeutic strategies for particular clinical situations. Early stage invasive breast cancer patients are commonly treated using breast conserving surgery (BCS) and radiotherapy (R/T). R/T is also widely used in the treatment of many brain cancers. Although treatment is often effective a significant proportion of individuals will develop local recurrence (LR), indicating a failure of primary therapy. A variety of clinico-pathological parameters are associated with risk of LR such as age, nodal status, tumour size, grade and vascular invasion. For breast cancer, the rate of LR is particularly high in women under the age of 40 and although LR rates can be
decreased by use of additional R/T, the associated LR rate is still, unfortunately, high. The reason why young women have such a worse prognosis remains unclear. Risk factors are used to assist patient stratification into low and high risk to determine initial treatment decisions but currently there is no method of identifying those patients at high risk of developing LR after therapy. There is, therefore, a need for biomarkers of response to allow more effective treatment, particularly as survival after relapse is poor, especially if diagnosed within 2 years after BCS.

The cytotoxicity of conventional R/T, is primarily mediated via the production of reactive oxygen species (ROS) and free radicals, that leads to increased oxidative stress, lipid and protein peroxidation, DNA damage and cell death. Redox buffering systems, signalling pathways and DNA repair systems are often deregulated in cancer cells and can interfere with the effectiveness of R/T. A number of studies have shown, in vitro, that the regulation of R/T response is complex with a number of pathways being interlinked. This project will examine expression of specific proteins in cancer, concentrating on breast and brain cancers, via histopathology based techniques and correlate response to R/T. It will also, using a variety of in vitro systems (2D and novel 3D), use agents to modify important, clinically relevant, targets to improve therapeutic response. As hypoxia is a major contributor to radioresistance drug efficacy will be examined under both normoxic and hypoxic conditions (single agent and combined with radiation).

Please email a CV with a covering letter to Professor Stewart Martin ( ), who can also supply more information to interested parties.




School of Medicine

University of Nottingham
Medical School
Nottingham, NG7 2UH

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