4.6 Article

An innovative single-base extension method for synchronous detection of point mutations and MSI status in colorectal cancer

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CANCER MEDICINE
卷 12, 期 7, 页码 8367-8377

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WILEY
DOI: 10.1002/cam4.5557

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colorectal cancer; MASE-CE; MSI; single-base extension; timesaver

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A new method called MASE-CE has been developed for genotyping analysis in patients with colorectal cancer. It can simultaneously detect KRAS/NRAS/BRAF gene mutations and microsatellite instability (MSI) status. The method showed high consistency with NGS and PCR-CE, and had superior sensitivity in mutation and MSI detection. This time-saving and specimen-saving method can provide timely clinical decision support.
Background: An accurate genotyping analysis is one of the critical prerequisites for patients with colorectal cancer receiving matched therapies. Conventional genotyping analysis is currently used to detect either gene mutations or MSI status, delaying the detection of critical tumor biomarkers and thus the optimal time for treatment. An assay that analyzes both biomarkers in a streamlined process is eagerly needed. Methods: We developed an assay combining Multiplex PCR Amplification, Single-base Extension and capillary electrophoresis (CE) analysis (MASE-CE) for synchronous detection of KRAS/NRAS/BRAF mutations and MSI status. In a 190 colorectal cancer cohort, we identified seven somatic mutations in KRAS, NRAS and BRAF as well as five MSI loci (D2S123/D5S346/D17S250/BAT-25/BAT-26) simultaneously. KRAS/NRAS/BRAF mutations were detected by NGS and MASE-CE, and MSI status were detected by PCR-CE and MASE-CE methods. Results: The MASE-CE method showed high consistency with NGS for mutation detection (Kappa value >= 0.8) and PCR-CE (Kappa value = 0.79). In addition, the limits of detection (LOD) of MASE-CE assay for MSI and somatic mutation were 5% and 2%, respectively. Conclusions: In somatic mutation detection and MSI detection, the LOD of MASE-CE assay was superior to that of qPCR and NGS. MASE-CE assay is a highly sensitive, time-saving and specimen-saving method, which can greatly avoid the cumbersome testing process and provide clinical decision for doctors in time.

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