Abstract

This paper estimates the yields of DNA double-strand breaks (DSBs) induced by ultrasoft X-rays and uses the DSB yields and the repair outcomes to evaluate the relative biological effectiveness (RBE) of ultrasoft X-rays. We simulated the yields of DSB induction and predicted them in the presence and absence of oxygen, using a Monte Carlo damage simulation (MCDS) software, to calculate the RBE. Monte Carlo excision repair (MCER) simulations were also performed to calculate the repair outcomes (correct repairs, mutations, and DSB conversions). Compared to 60Co γ-rays, the RBE values for ultrasoft X-rays (titanium K-shell, aluminum K-shell, copper L-shell, and carbon K-shell) for DSB induction were respectively 1.3, 1.9, 2.3, and 2.6 under aerobic conditions and 1.3, 2.1, 2.5, and 2.9 under a hypoxic condition (2% O2). The RBE values for enzymatic DSBs were 1.6, 2.1, 2.3, and 2.4, respectively, indicating that the enzymatic DSB yields are comparable to the yields of DSB induction. The synergistic effects of DSB induction and enzymatic DSB formation further facilitate cell killing and the advantage in cancer treatment.

Highlights

  • The relative biological effectiveness (RBE) depends on photon energy

  • The results show that the nucleotide excision repair (NER)/LP base excision repair (BER) pathway has the lowest probability of correct repair and highest probability for mutation and double-strand breaks (DSBs) formation, which is similar to the results for 60 Co γ-rays [44], protons [40], and helium ions [44]

  • The RBE calculated from the measured DSB induction relative to 60 Co γ-rays increased from 1.4 to 2.7 as the photon energy decreased from 4.55 keV to 280 eV [3]

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Summary

Introduction

The relative biological effectiveness (RBE) depends on photon energy. In particular, RBE of ultrasoft X-rays (

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