“Micronuclei and Disease” special issue: Aims, scope, and synthesis of outcomes

IF 6.4 2区 医学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Michael Fenech , Siegfried Knasmueller , Lisbeth E. Knudsen , Micheline Kirsch-Volders , Permal Deo , Bernhard Franzke , Helga Stopper , Maria-Grazia Andreassi , Claudia Bolognesi , Varinderpal S. Dhillon , Blanca Laffon , Karl-Heinz Wagner , Stefano Bonassi
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引用次数: 16

Abstract

The purpose of the “Micronuclei and Disease” special issue (SI) is to: (i) Determine the level of evidence for association of micronuclei (MN), a biomarker of numerical and structural chromosomal aberrations, with risk of specific diseases in humans; (ii) Define plausible mechanisms that explain association of MN with each disease; (iii) Identify knowledge gaps and research needed to translate MN assays into clinical practice.

The “MN and Disease” SI includes 14 papers. The first is a review of mechanisms of MN formation and their consequences in humans. 11 papers are systematic reviews and/or meta-analyses of the association of MN with reproduction, child health, inflammation, auto-immune disease, glycation, metabolic diseases, chronic kidney disease, cardiovascular disease, eleven common cancers, ageing and frailty. The penultimate paper focuses on effect of interventions on MN frequency in the elderly. A road map for translation of MN data into clinical practice is the topic of the final paper.

The majority of reviewed studies were case-control studies in which the ratio of mean MN frequency in disease cases relative to controls, i.e. the mean ratio (MR), was calculated. The mean of these MR values, estimated by meta-analyses, for lymphocyte and buccal cell MN in non-cancer diseases were 2.3 and 3.6 respectively, and for cancers they were 1.7 and 2.6 respectively. The highest MR values were observed in studies of cancer cases in which MN were measured in the same tissue as the tumour (MR = 4.9–10.8).

This special issue is an important milestone in the evidence supporting MN as a reliable genomic biomarker of developmental and degenerative disease risk. These advances, together with results from prospective cohort studies, are helping to identify diseases in which MN assays can be practically employed in the clinical setting to better identify high risk patients and to prioritise them for preventive therapy.

"微核与疾病"特刊:目标、范围和成果综合
"微核与疾病"特刊的目的是:(i)确定微核(数量和结构染色体畸变的生物标志物)与人类特定疾病风险之间关联的证据水平;(ii)确定MN与每种疾病之间关联的合理机制;(iii)确定将MN检测方法转化为临床实践所需的知识缺口和研究。“MN与疾病”SI收录了14篇论文。第一篇综述了锰形成的机制及其对人类的影响。11篇论文是关于MN与生殖、儿童健康、炎症、自身免疫性疾病、糖基化、代谢疾病、慢性肾脏疾病、心血管疾病、11种常见癌症、衰老和虚弱之间关系的系统综述和/或荟萃分析。倒数第二篇论文的重点是干预对老年人MN频率的影响。最后一篇论文的主题是将MN数据转化为临床实践的路线图。大多数审查的研究是病例对照研究,其中计算疾病病例中MN平均频率相对于对照组的比率,即平均比率(MR)。通过荟萃分析估计,非癌症疾病中淋巴细胞和颊细胞MN的MR平均值分别为2.3和3.6,癌症的MR平均值分别为1.7和2.6。在与肿瘤在同一组织中测量MN的癌症病例研究中观察到最高的MR值(MR = 4.9-10.8)。这一期特刊是支持MN作为发育性和退行性疾病风险可靠的基因组生物标志物的重要里程碑。这些进展,加上前瞻性队列研究的结果,正在帮助识别疾病,其中MN测定可以在临床环境中实际应用,以更好地识别高风险患者并优先进行预防治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
12.20
自引率
1.90%
发文量
22
审稿时长
15.7 weeks
期刊介绍: The subject areas of Reviews in Mutation Research encompass the entire spectrum of the science of mutation research and its applications, with particular emphasis on the relationship between mutation and disease. Thus this section will cover advances in human genome research (including evolving technologies for mutation detection and functional genomics) with applications in clinical genetics, gene therapy and health risk assessment for environmental agents of concern.
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