EPSRC Reference: |
GR/S56283/02 |
Title: |
The influence of high Z atoms on the generation of complex DNA lesions by ionizing radiation: implications for radiotherapy |
Principal Investigator: |
Hirst, Professor D |
Other Investigators: |
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Researcher Co-Investigators: |
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Project Partners: |
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Department: |
Sch of Pharmacy |
Organisation: |
Queen's University of Belfast |
Scheme: |
Standard Research (Pre-FEC) |
Starts: |
01 October 2004 |
Ends: |
30 September 2007 |
Value (£): |
160,731
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EPSRC Research Topic Classifications: |
Medical science & disease |
Scattering & Spectroscopy |
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EPSRC Industrial Sector Classifications: |
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Related Grants: |
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Panel History: |
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Summary on Grant Application Form |
Radiotherapy remains one of the most effective forms of cancer treatment. Ionisation, leading to DNA strand breaks is one of the dominant energy absorption mechanisms for radiation of this quality. A small proportion of these breaks are not accurately repaired and result in death of cancer cells. Irradiation with heavy charged particles deposits a large amount of energy in a small volume, generating multiply-damaged sites, which are very poorly repaired and are thus highly cytotoxic. However, heavy ion beam generators are hugely expensive and currently impractical for routine clinical use, but we believe it may be possible to enhance the generation of multiply-damaged sites in DNA by a simpler mechanism. If atoms with high atomic number (Z) could be preferentially localised within tumours, their large cross section would result in multiple ionisation within a small volume. As the space charge of the multiply ionised sites can induce large amounts of Coulomb repulsion force within DNA molecules, substantial strand/bond breakage can ensue as charged fragments fly away from the sites. This would result in highly efficient cell killing and would complement the spatial targeting that is an inherent advantage of radiotherapy. Our aim is to gain an understanding of the molecular events resulting from DNA irradiation in the presence or absence of atoms with a range of (high) Z values. We will use a variety of techniques, including pulsed field gell electrophoresis and atomic force microscopy to investigate the nature of these lesions and correlate the findings with analyses of ejected molecular species using time of flight mass spectroscopy. The results obtained will be used to inform future developments of this approach in vitro and in vivo
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Key Findings |
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Potential use in non-academic contexts |
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Impacts |
Description |
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Summary |
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Date Materialised |
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Sectors submitted by the Researcher |
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Project URL: |
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Further Information: |
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Organisation Website: |
http://www.qub.ac.uk |