Konopacka Maria, Rogoliński Jacek, Sochanik Aleksander, Ślosarek Krzysztof
Centre for Translational Research and Molecular Biology of Cancer, Maria Skłodowska-Curie Memorial Cancer Centre and Institute of Oncology Gliwice Branch, Gliwice, Poland.
Department of Radiotherapy and Brachytherapy Planning, Maria Skłodowska-Curie Memorial Cancer Centre and Institute of Oncology Gliwice Branch, Gliwice, Poland.
Contemp Oncol (Pozn). 2016;20(6):449-452. doi: 10.5114/wo.2016.65603. Epub 2017 Jan 12.
Current cancer radiotherapy relies on increasingly high dose rates of ionising radiation (100-2400 cGy/min). It is possible that changing dose rates is not paralleled by treatment effectiveness. Irradiating cancer cells is assumed to induce molecular alterations that ultimately lead to apoptotic death. Studies comparing the efficacy of radiation-induced DNA damage and apoptotic death in relation to varying dose rates do not provide unequivocal data. Whereas some have demonstrated higher dose rates (single dose) to effectively kill cancer cells, others claim the opposite. Recent gene expression studies in cells subject to variable dose rates stress alterations in molecular signalling, especially in the expression of genes linked to cell survival, immune response, and tumour progression. Novel irradiation techniques of modern cancer treatment do not rely anymore on maintaining absolute constancy of dose rates during radiation emission: instead, timing and exposure areas are regulated temporally and spatially by modulating the dose rate and beam shape. Such conditions may be reflected in tumour cells' response to irradiation, and this is supported by the references provided.
当前的癌症放射治疗依赖于越来越高剂量率的电离辐射(100 - 2400 厘戈瑞/分钟)。剂量率的改变与治疗效果可能并不平行。照射癌细胞被认为会诱导分子改变,最终导致凋亡死亡。关于不同剂量率下辐射诱导的 DNA 损伤和凋亡死亡疗效的比较研究并未提供明确的数据。虽然一些研究表明较高剂量率(单次剂量)能有效杀死癌细胞,但另一些研究则持相反观点。最近对接受不同剂量率照射的细胞进行的基因表达研究强调了分子信号传导的改变,特别是与细胞存活、免疫反应和肿瘤进展相关基因的表达变化。现代癌症治疗的新型照射技术不再依赖于在辐射发射过程中保持剂量率的绝对恒定:相反,通过调节剂量率和光束形状在时间和空间上对照射时间和区域进行调控。这些情况可能反映在肿瘤细胞对辐射的反应中,所提供的参考文献也支持了这一点。