Makurat Samanta, Chomicz-Mańka Lidia, Rak Janusz
Faculty of Chemistry, University of Gdańsk, Wita Stwosza 63, 80-308, Gdańsk, Poland.
Chemphyschem. 2016 Aug 18;17(16):2572-8. doi: 10.1002/cphc.201600240. Epub 2016 May 24.
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.
尽管5-溴-2'-脱氧尿苷(5BrdU)在体外具有显著的放射增敏能力,但临床研究并未证实使用5BrdU进行放射治疗有任何优势。这种情况需要持续寻找有效的放射增敏剂。利用所提出的5BrdU放射增敏机制,我们提出了一系列5-取代尿嘧啶XYU,它们应能经历有效的离解电子附着。关于电子加成诱导的XYU降解的密度泛函理论(DFT)计算的热力学和动力学数据表明,一些经过仔细研究的衍生物具有比5BrdU本身更好的特性。合成这些有前景的放射增敏剂候选物,随后研究它们在DNA环境中以及最终在癌细胞中的放射增敏特性,是进一步确认它们在抗癌治疗中潜在适用性的步骤。