Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom.
Pathology Department and Northern Genetics Service, Newcastle Hospitals, NHS Foundation Trust, Newcastle upon Tyne, United Kingdom.
PLoS One. 2018 Aug 29;13(8):e0203052. doi: 10.1371/journal.pone.0203052. eCollection 2018.
Somatic mutations in mononucleotide repeats are commonly used to assess the mismatch repair status of tumours. Current tests focus on repeats with a length above 15bp, which tend to be somatically more unstable than shorter ones. These longer repeats also have a substantially higher PCR error rate, and tests that use capillary electrophoresis for fragment size analysis often require expert interpretation. In this communication, we present a panel of 17 short repeats (length 7-12bp) for sequence-based microsatellite instability (MSI) testing. Using a simple scoring procedure that incorporates the allelic distribution of the mutant repeats, and analysis of two cohort of tumours totalling 209 samples, we show that this panel is able to discriminate between MMR proficient and deficient tumours, even when constitutional DNA is not available. In the training cohort, the method achieved 100% concordance with fragment analysis, while in the testing cohort, 4 discordant samples were observed (corresponding to 97% concordance). Of these, 2 showed discrepancies between fragment analysis and immunohistochemistry and one was reclassified after re-testing using fragment analysis. These results indicate that our approach offers the option of a reliable, scalable routine test for MSI.
核苷酸重复序列中的体细胞突变通常用于评估肿瘤的错配修复状态。目前的检测集中在长度超过 15bp 的重复序列上,这些重复序列往往比短重复序列更不稳定。这些较长的重复序列也具有更高的 PCR 错误率,而使用毛细管电泳进行片段大小分析的检测通常需要专家解释。在本通讯中,我们提出了一组 17 个短重复序列(长度为 7-12bp)用于基于序列的微卫星不稳定性(MSI)检测。使用一种简单的评分程序,该程序整合了突变重复序列的等位基因分布,并对总共 209 个样本的两个肿瘤队列进行了分析,我们表明该面板能够区分 MMR 功能正常和功能缺失的肿瘤,即使没有获得体质 DNA 也是如此。在训练队列中,该方法与片段分析达到了 100%的一致性,而在测试队列中,观察到 4 个不一致的样本(对应于 97%的一致性)。其中,2 个样本在片段分析和免疫组织化学之间存在差异,一个样本在使用片段分析重新测试后重新分类。这些结果表明,我们的方法为 MSI 提供了一种可靠、可扩展的常规检测方法。