Elmendorff-Dreikorn K, Chauvin C, Slor H, Kutzner J, Batel R, Müller W E, Schröder H C
Klinik und Poliklinik für Radiologie, Klinikum der Johannes Gutenberg-Universität, Mainz, Germany.
Cell Mol Biol (Noisy-le-grand). 1999 Mar;45(2):211-8.
A newly developed, fast and sensitive microplate assay (Fast Micromethod) was used for the assessment of gamma-radiation-induced DNA damage in peripheral blood mononuclear cells (PBMC) from healthy donors of various ages and from cancer patients undergoing radiotherapy. This assay detects the presence of DNA single-strand breaks and alkali-labile sites by monitoring the rate of DNA unwinding under alkaline conditions using the fluorescent dye PicoGreen, which preferentially binds to double-stranded DNA at high pH (>12.0); it requires only minimal amounts of material (approximately 3 x 10(3) cells/well) and can be performed within 3 hrs. or less. EDTA blood samples were collected from patients not undergoing chemotherapy prior and immediately after irradiation, or were collected from healthy donors and irradiated ex vivo. The results revealed that the amount of DNA strand breaks in PBMC, induced by application of a single dose to patients in the course of radiotherapy treatment, markedly varied between different individuals. To examine the effect of age on DNA damage, the basal levels of DNA damage in PBMC from a total of 30 healthy donors were determined: 10 were 20 to 30 years of age, 10 were 40 to 60 years of age and 10 were >70 years of age. It was found that the mean basal level of DNA damage from donors in the >70-year age group was significantly higher (by 97%) than that of the 20- to 30-year age group and 27% higher than that of the 40- to 60-year age group. Measurements of the level of induced DNA damage in PBMC isolated from blood after 2 Gy irradiation with 60Co gamma-rays revealed no significant differences between donors aged 20-30 and 40-60. However, there was a strong increase (by 2.3- to 2.9-fold) in radiosensitivity in the age group >70. The microplate assay described may be used as a pretherapeutic sensitivity test for the assessment of the individual radiosensitivity of patients prior to radiation therapy.
一种新开发的快速灵敏的微孔板检测法(快速微量法)用于评估不同年龄健康供者以及接受放疗的癌症患者外周血单个核细胞(PBMC)中γ射线诱导的DNA损伤。该检测法通过使用荧光染料PicoGreen监测碱性条件下DNA解旋速率来检测DNA单链断裂和碱不稳定位点的存在,PicoGreen在高pH值(>12.0)时优先结合双链DNA;它只需要极少量的材料(约3×10³个细胞/孔),并且可以在3小时或更短时间内完成。从未接受化疗的患者放疗前和放疗后立即采集EDTA血样,或者从健康供者采集血样并进行离体照射。结果显示,在放疗过程中对患者单次给药诱导的PBMC中DNA链断裂量在不同个体之间有显著差异。为了研究年龄对DNA损伤的影响,测定了总共30名健康供者PBMC中DNA损伤的基础水平:10名年龄在20至30岁,10名年龄在40至60岁,10名年龄大于70岁。发现年龄大于70岁组供者的DNA损伤平均基础水平显著高于20至30岁组(高97%),比40至60岁组高27%。对用⁶⁰Coγ射线2 Gy照射后从血液中分离出的PBMC中诱导的DNA损伤水平进行测量,结果显示20至30岁和40至60岁的供者之间没有显著差异。然而,年龄大于70岁组的放射敏感性有显著增加(增加2.3至2.9倍)。所描述的微孔板检测法可作为放疗前敏感性检测,用于评估患者放疗前的个体放射敏感性。