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毛细管电泳工作流程在结直肠癌微卫星不稳定性分析和错配修复(MMR)免疫组化染色中的高度一致性。

High concordance rate of capillary electrophoresis workflow for microsatellite instability analysis and mismatch repair (MMR) immunostaining in colorectal carcinoma.

机构信息

Department of Pathology, Molecular Diagnosis Laboratory, National Cheng Kung University Hospital, Tainan, Taiwan.

Molecular Medicine Core Laboratory, Research Center of Clinical Medicine, National Cheng Kung University Hospital, Tainan, Taiwan.

出版信息

PLoS One. 2023 Apr 25;18(4):e0284227. doi: 10.1371/journal.pone.0284227. eCollection 2023.

Abstract

Microsatellite instability (MSI) is the primary predictive biomarker for therapeutic efficacies of cancer immunotherapies. Establishment of the MSI detection methods with high sensitivity and accessibility is important. Because MSI is mainly caused by defects in DNA mismatch repair (MMR), immunohistochemical (IHC) staining for the MMR proteins has been widely employed to predict the responses to immunotherapies. Thus, due to the high sensitivity of PCR, the MSI-PCR analysis has also been recommended as the primary approach as MMR IHC. This study aimed to develop a sensitive and convenient platform for daily MSI-PCR services. The routine workflow used a non-labeling QIAxcel capillary electrophoresis system which did not need the fluorescence labeling of the DNA products or usage of a multi-color fluorescence reader. Furthermore, the 15 and 1000 bp size alignment markers were used to precisely detect the size of the DNA product. A cohort of 336 CRC cases was examined by MSI-PCR on the five mononucleotide MSI markers recommended by ESMO. The PCR products were analyzed in the screening gels, followed by high-resolution gel electrophoresis for confirmation if needed. In the MSI-PCR tests, 90.1% (303/336) cases showed clear major shift patterns in the screening gels, and only 33 cases had to be re-examined using the high-resolution gels. The cohort was also analyzed by MMR IHC is, which revealed 98.5% (331/336) concordance with MSI-PCR. In the five discordant cases, 4 (3 MSI-L and 1 MSS) showed MSH6 loss. Besides, one case exhibited MSI-H but no loss in the MMR IHC. Further NGS analysis, in this case, found that missense and frameshift mutations in the PMS2 and MSH6 genes occurred, respectively. In conclusion, the non-labeling MSI-PCR capillary electrophoresis revealed high concordance with the MMR IHC analysis and is cost- and time-effective. Therefore, it shall be highly applicable in clinical laboratories.

摘要

微卫星不稳定性(MSI)是癌症免疫疗法治疗效果的主要预测生物标志物。建立高灵敏度和易获取的 MSI 检测方法非常重要。由于 MSI 主要是由 DNA 错配修复(MMR)缺陷引起的,因此免疫组织化学(IHC)染色 MMR 蛋白已被广泛用于预测免疫治疗的反应。因此,由于 PCR 的高灵敏度,MSI-PCR 分析也被推荐作为 MMR IHC 的主要方法。本研究旨在开发一种用于日常 MSI-PCR 服务的敏感便捷平台。常规工作流程使用非标记的 QIAxcel 毛细管电泳系统,该系统不需要 DNA 产物的荧光标记,也不需要使用多色荧光读取器。此外,使用 15 和 1000 bp 大小的对齐标记物来精确检测 DNA 产物的大小。对一组 336 例 CRC 病例进行了 ESMO 推荐的五种单核苷酸 MSI 标志物的 MSI-PCR 检测。在筛选凝胶中分析 PCR 产物,如果需要,再进行高分辨率凝胶电泳进行确认。在 MSI-PCR 测试中,90.1%(303/336)的病例在筛选凝胶中显示出明显的主要移位模式,只有 33 例需要使用高分辨率凝胶重新检测。该队列也进行了 MMR IHC 分析,结果与 MSI-PCR 显示 98.5%(331/336)的一致性。在 5 个不一致的病例中,4 个(3 个 MSI-L 和 1 个 MSS)表现出 MSH6 缺失。此外,有一个病例表现为 MSI-H,但 MMR IHC 无缺失。进一步的 NGS 分析发现,该病例中 PMS2 和 MSH6 基因分别发生错义突变和移码突变。总之,非标记 MSI-PCR 毛细管电泳与 MMR IHC 分析具有高度一致性,具有成本效益和时间效益。因此,它将非常适用于临床实验室。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d396/10128978/9d74e56be81f/pone.0284227.g001.jpg

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