Vral A, Thierens H, Baeyens A, De Ridder L
Department of Anatomy, Embryology, Histology and Medical Physics, University of Gent, L. Pasteurlaan 2, 9000 Gent, Belgium.
Toxicol Lett. 2004 Apr 1;149(1-3):345-52. doi: 10.1016/j.toxlet.2003.12.044.
In order to assess the applicability of the micronucleus (MN) and G2 assays as biomarkers of in vitro radiosensitivity and cancer susceptibility, we investigated the inter- and intra-individual variation of these endpoints. For the MN assay unstimulated blood cultures from 57 healthy donors were exposed in vitro to 3.5 Gy Co gamma-rays and for the G2 assay PHA stimulated cultures were irradiated with a dose of 0.4 Gy Co gamma-rays in the G2 phase of the cell cycle. For 14 donors, 2-15 repeat samples were tested over a period of 3 years. The repeat experiments revealed that the intra-individual variability was not significantly different from the inter-individual variability for both G2 and MN assays. As the intra-individual variability determines the reproducibility of the assay, our results highlight the limitations of these endpoints in detecting reproducible differences in radiation sensitivity between individuals within a normal population. Due to the high intra-individual variability and no significant difference with the inter-individual variability found in our study we conclude that care has to be taken when results obtained with chromosomal aberration assays based on one blood sample are used to assess the individual radiosensitivity. Multiple blood sampling may be necessary to draw reliable conclusions. Although more validation studies on the reliability of the G2 and MN assay will be required before they can be used in a confident way as biomarkers of individual radiosensitivity or cancer susceptibility the assays are very valuable to examine population radiosensitivity and the relationship between radiosensitivity, cancer predisposition and genotype.
为了评估微核(MN)和G2检测作为体外放射敏感性和癌症易感性生物标志物的适用性,我们研究了这些终点指标在个体间和个体内的变异情况。对于MN检测,来自57名健康供体的未刺激血液培养物在体外接受3.5 Gy的钴γ射线照射;对于G2检测,在细胞周期的G2期,用0.4 Gy的钴γ射线照射PHA刺激的培养物。对于14名供体,在3年的时间内进行了2 - 15次重复样本检测。重复实验表明,对于G2和MN检测,个体内变异性与个体间变异性没有显著差异。由于个体内变异性决定了检测的可重复性,我们的结果突出了这些终点指标在检测正常人群中个体间放射敏感性可重复差异方面的局限性。由于我们的研究中个体内变异性高且与个体间变异性无显著差异,我们得出结论,当基于一份血样的染色体畸变检测结果用于评估个体放射敏感性时必须谨慎。可能需要多次采血才能得出可靠结论。尽管在能够自信地将G2和MN检测用作个体放射敏感性或癌症易感性生物标志物之前,还需要更多关于其可靠性的验证研究,但这些检测对于检查人群放射敏感性以及放射敏感性、癌症易感性和基因型之间的关系非常有价值。