Electrophilic 5-Substituted Uracils as Potential Radiosensitizers: A Density Functional Theory Study

Chemphyschem. 2016 Aug 18;17(16):2572-8. doi: 10.1002/cphc.201600240. Epub 2016 May 24.

Abstract

Although 5-bromo-2'-deoxyuridine (5BrdU) possesses significant radiosensitizing power in vitro, clinical studies do not confirm any advantages of radiotherapy employing 5BrdU. This situation calls for a continuous search for efficient radiosensitizers. Using the proposed mechanism of radiosensitization by 5BrdU, we propose a series of 5-substituted uracils, XYU, that should undergo efficient dissociative electron attachment. The DFT-calculated thermodynamic and kinetic data concerning the XYU degradations induced by electron addition suggests that some of the scrutinized derivatives have much better characteristics than 5BrdU itself. Synthesis of these promising candidates for radiosensitizers, followed by studies of their radiosensitizing properties in DNA context, and ultimately in cancer cells, are further steps to confirm their potential applicability in anticancer treatment.

Keywords: DNA; density functional calculations; dissociative electron attachment; nucleobases; radiopharmaceuticals.

MeSH terms

  • Models, Molecular
  • Molecular Structure
  • Quantum Theory*
  • Radiation-Sensitizing Agents / chemistry*
  • Uracil / analogs & derivatives
  • Uracil / chemistry*

Substances

  • Radiation-Sensitizing Agents
  • Uracil