The superior dose distribution of particle radiation compared to photon radiation makes it a promising therapy for the treatment of tumors. However, the cellular responses to particle therapy and especially the DNA damage response (DDR) is not well characterized. Compared to photons, particles are thought to induce more closely spaced DNA lesions instead of isolated lesions. How this different spatial configuration of the DNA damage directs DNA repair pathway usage, is subject of current investigations. In this review, we describe recent insights into induction of DNA damage by particle radiation and how this shapes DNA end processing and subsequent DNA repair mechanisms. Additionally, we give an overview of promising DDR targets to improve particle therapy.
Bibliographical noteFunding Information:
This work was supported by the Dutch Cancer Society (INTO-PROT, 12092/2018) and Varian (PROTON-DDR, 2019020), and is part of the Oncode Institute, which was partly financed by the Dutch Cancer Society.
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