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A Computational Model of Cellular Response to Modulated Radiation Fields

  • Stephen J. McMahon, Ph.D.

      Affiliations

    • Centre for Cancer Research and Cell Biology, Queen’s University Belfast, Belfast, Northern Ireland, United Kingdom
    • Corresponding Author InformationReprint requests to: Dr. Stephen J. McMahon, Centre for Cancer Research and Cell Biology, Queens University Belfast, 97 Lisburn Road, Belfast BT9 7BL, Northern Ireland, United Kingdom. Tel: (44) 2890 972779; Fax: (44) 2890 972776
  • ,
  • Karl T. Butterworth, Ph.D.

      Affiliations

    • Centre for Cancer Research and Cell Biology, Queen’s University Belfast, Belfast, Northern Ireland, United Kingdom
  • ,
  • Conor K. McGarry, M.Sc.

      Affiliations

    • Centre for Cancer Research and Cell Biology, Queen’s University Belfast, Belfast, Northern Ireland, United Kingdom
    • Radiotherapy Physics, Northern Ireland Cancer Centre, Belfast Health and Social Care Trust, Northern Ireland, United Kingdom
  • ,
  • Colman Trainor, B.Sc.

      Affiliations

    • Centre for Cancer Research and Cell Biology, Queen’s University Belfast, Belfast, Northern Ireland, United Kingdom
  • ,
  • Joe M. O’Sullivan, FRR(RCSI)

      Affiliations

    • Centre for Cancer Research and Cell Biology, Queen’s University Belfast, Belfast, Northern Ireland, United Kingdom
    • Clinical Oncology, Northern Ireland Cancer Centre, Belfast Health and Social Care Trust, Belfast, Northern Ireland, United Kingdom
  • ,
  • Alan R. Hounsell, Ph.D.

      Affiliations

    • Centre for Cancer Research and Cell Biology, Queen’s University Belfast, Belfast, Northern Ireland, United Kingdom
    • Radiotherapy Physics, Northern Ireland Cancer Centre, Belfast Health and Social Care Trust, Northern Ireland, United Kingdom
  • ,
  • Kevin M. Prise, Ph.D.

      Affiliations

    • Centre for Cancer Research and Cell Biology, Queen’s University Belfast, Belfast, Northern Ireland, United Kingdom

Received 22 July 2011; received in revised form 11 October 2011; accepted 24 October 2011. published online 27 January 2012.
Corrected Proof

Purpose

To develop a model to describe the response of cell populations to spatially modulated radiation exposures of relevance to advanced radiotherapies.

Materials and Methods

A Monte Carlo model of cellular radiation response was developed. This model incorporated damage from both direct radiation and intercellular communication including bystander signaling. The predictions of this model were compared to previously measured survival curves for a normal human fibroblast line (AGO1522) and prostate tumor cells (DU145) exposed to spatially modulated fields.

Results

The model was found to be able to accurately reproduce cell survival both in populations which were directly exposed to radiation and those which were outside the primary treatment field. The model predicts that the bystander effect makes a significant contribution to cell killing even in uniformly irradiated cells. The bystander effect contribution varies strongly with dose, falling from a high of 80% at low doses to 25% and 50% at 4 Gy for AGO1522 and DU145 cells, respectively. This was verified using the inducible nitric oxide synthase inhibitor aminoguanidine to inhibit the bystander effect in cells exposed to different doses, which showed significantly larger reductions in cell killing at lower doses.

Conclusions

The model presented in this work accurately reproduces cell survival following modulated radiation exposures, both in and out of the primary treatment field, by incorporating a bystander component. In addition, the model suggests that the bystander effect is responsible for a significant portion of cell killing in uniformly irradiated cells, 50% and 70% at doses of 2 Gy in AGO1522 and DU145 cells, respectively. This description is a significant departure from accepted radiobiological models and may have a significant impact on optimization of treatment planning approaches if proven to be applicable in vivo.

Keywords: Bystander, Cell survival, Modulated beams, Monte Carlo, Out-of-field

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 This work was supported by grants from Cancer Research UK (no. C1513/A7047 to K.M.P., and no. C212/A11342 to S.M. and A.R.H.). C.K.M. is supported by a Health and Social Care Research and Development of the Public Health Agency training fellowship award. C.T. is supported by a DEL studentship.

 Conflict of interest: none.

PII: S0360-3016(11)03466-3

doi:10.1016/j.ijrobp.2011.10.058

« BackInternational Journal of Radiation Oncology * Biology * Physics