Bonassi Stefano, Biasotti Barbara, Kirsch-Volders Micheline, Knasmueller Siegfried, Zeiger Errol, Burgaz Sema, Bolognesi Claudia, Holland Nina, Thomas Philip, Fenech Michael
Mutagenesis. 2009 Jul;24(4):295-302. doi: 10.1093/mutage/gep019. Epub 2009 May 28.
The study of DNA damage in exfoliated buccal cells is a minimally invasive method for monitoring populations for exposure to genotoxic agents. The presence of micronuclei (MN) and other nuclear anomalies within these cells has been shown to be associated with genetic defects in genome maintenance, accelerated ageing, genotoxic damage and some degenerative diseases. To identify important information gaps regarding these biomarkers, a new initiative was launched within the framework of the HUman MicroNucleus (HUMN) collaborative programme, the HUMN(XL) project ('XL' designating eXfoLiated cell). An invitation to join the project was sent out together with a questionnaire to all laboratories that have published on the buccal micronucleus assay. Overall, 188 messages were delivered and 58 laboratories from 25 countries agreed to participate (43 contributing data). The questionnaire was designed to collect methodological information regarding the laboratory's performance of the assay and to assess the extent and type of epidemiological data that are routinely collected. The results provide an overview of the most commonly used methods for buccal cell collection and preparation, slide preparation, staining, scoring criteria and an evaluation of epidemiological data, including demographics, genetic background, gender, health status, occupation, exposure, lifestyle and dietary habit. According to this survey, a potential base of 15 103 subjects can be included in future pooled analyses. A number of protocol discrepancies emerged, implying that method standardization is a major priority. The results of this survey will contribute to (i) identify technical and epidemiological key variables that impact on buccal MN frequency in human populations, (ii) drive the design of future intra- and interlaboratory validation studies and (iii) determine the role of MN frequency and other biomarkers, in monitoring genomic damage and predicting cancer and other degenerative diseases.
研究脱落颊细胞中的DNA损伤是一种微创方法,用于监测人群接触遗传毒性剂的情况。这些细胞中微核(MN)和其他核异常的存在已被证明与基因组维持中的遗传缺陷、加速衰老、遗传毒性损伤和一些退行性疾病有关。为了确定关于这些生物标志物的重要信息差距,在人类微核(HUMN)合作计划的框架内启动了一项新举措,即HUMN(XL)项目(“XL”表示脱落细胞)。向所有发表过颊黏膜微核试验的实验室发出了加入该项目的邀请,并附上了一份问卷。总体而言,共发送了188条信息,来自25个国家的58个实验室同意参与(43个提供了数据)。该问卷旨在收集有关实验室检测方法的信息,并评估常规收集的流行病学数据的范围和类型。结果概述了颊细胞收集和制备、载玻片制备、染色、评分标准等最常用的方法,以及对流行病学数据的评估,包括人口统计学、遗传背景、性别、健康状况、职业、接触情况、生活方式和饮食习惯。根据这项调查,未来的汇总分析中可能纳入15103名受试者。出现了一些方案差异,这意味着方法标准化是一个主要优先事项。这项调查的结果将有助于:(i)确定影响人群颊黏膜微核频率的技术和流行病学关键变量;(ii)推动未来实验室内部和实验室间验证研究的设计;(iii)确定微核频率和其他生物标志物在监测基因组损伤以及预测癌症和其他退行性疾病方面的作用。