EMQN实体肿瘤微卫星不稳定性分析和报告最佳实践指南。

IF 4.6 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Richard Gallon, Liam McCormick, Angelica Saetta, Cristina Albuquerque, Samantha Butler, Treena Cranston, Joanne Field, Ciaron McAnulty, Patrícia Silva, Melanie Cheetham, Katie Sheils, George J Burghel
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引用次数: 0

摘要

微卫星不稳定性(Microsatellite instability, MSI)是短串联重复DNA序列(Microsatellite)中插入和删除变异(不稳定性)的累积。高水平的MSI发生在DNA错配修复系统(MMR)功能丧失后。MMR缺乏是一种越来越重要的癌症生物标志物,与化疗耐药和免疫检查点阻断反应以及最常见的遗传性癌症综合征Lynch综合征有关。自二十多年前发现以来,我们对MSI分析的生物学理解、测试方法和临床意义迅速扩大,需要最新的最佳实践指南。一个专家工作组审查了文献并制定了15项最佳实践建议,这些建议在与EMQN合作的临床和实验室科学家协商后最终确定。其中包括关于MSI检测关键技术方面的七项建议和关于临床解释和结果报告的八项建议。后者侧重于Lynch综合征筛查和免疫检查点阻断治疗。提供了示例报告措辞,以帮助实现和标准化。还讨论了常用术语和MSI分析方法。这些指南主要针对在诊断测试实验室工作的基因组科学家,但也将为临床医生、学者和其他相关专业人员提供有用的MSI综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
EMQN best practice guidelines for analysis and reporting of microsatellite instability in solid tumours.

Microsatellite instability (MSI) is the accumulation of insertion and deletion variants (instability) in short tandem repeat DNA sequences (microsatellites). High levels of MSI occur following loss of function of the DNA mismatch repair system (MMR). MMR deficiency is an increasingly important cancer biomarker that is associated with chemotherapy resistance and response to immune checkpoint blockade, as well as one of the commonest hereditary cancer syndromes, Lynch syndrome. Since its discovery over two decades ago, our biological understanding, the testing methods, and the clinical implications of MSI analysis have expanded rapidly and up-to-date best practice guidelines are needed. An expert working group reviewed the literature and devised 15 best practice recommendations that were finalised following consultation with clinical and laboratory scientists partnered with EMQN. These include seven recommendations on key technical aspects of MSI testing and eight recommendations on the clinical interpretation and reporting of results. The latter focuses on Lynch syndrome screening and immune checkpoint blockade therapy. Example report wording is provided to assist implementation and standardisation. Common terminology and MSI analysis methods are also discussed. These guidelines are aimed primarily at genomic scientists working in diagnostic testing laboratories, but will provide a useful review of MSI for clinicians, academics, and other related professionals.

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来源期刊
European Journal of Human Genetics
European Journal of Human Genetics 生物-生化与分子生物学
CiteScore
9.90
自引率
5.80%
发文量
216
审稿时长
2 months
期刊介绍: The European Journal of Human Genetics is the official journal of the European Society of Human Genetics, publishing high-quality, original research papers, short reports and reviews in the rapidly expanding field of human genetics and genomics. It covers molecular, clinical and cytogenetics, interfacing between advanced biomedical research and the clinician, and bridging the great diversity of facilities, resources and viewpoints in the genetics community. Key areas include: -Monogenic and multifactorial disorders -Development and malformation -Hereditary cancer -Medical Genomics -Gene mapping and functional studies -Genotype-phenotype correlations -Genetic variation and genome diversity -Statistical and computational genetics -Bioinformatics -Advances in diagnostics -Therapy and prevention -Animal models -Genetic services -Community genetics
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