Biofidelity Ltd, 330 Cambridge Science Park, Cambridge, CB4 0WN, UK.
Agilent Technologies LDA UK Ltd, 5500 Lakeside, Cheadle, SK8 3GR, UK.
Sci Rep. 2021 Mar 16;11(1):6068. doi: 10.1038/s41598-021-85545-3.
Accurate detection of somatic variants, against a background of wild-type molecules, is essential for clinical decision making in oncology. Existing approaches, such as allele-specific real-time PCR, are typically limited to a single target gene and lack sensitivity. Alternatively, next-generation sequencing methods suffer from slow turnaround time, high costs, and are complex to implement, typically limiting them to single-site use. Here, we report a method, which we term Allele-Specific PYrophosphorolysis Reaction (ASPYRE), for high sensitivity detection of panels of somatic variants. ASPYRE has a simple workflow and is compatible with standard molecular biology reagents and real-time PCR instruments. We show that ASPYRE has single molecule sensitivity and is tolerant of DNA extracted from plasma and formalin fixed paraffin embedded (FFPE) samples. We also demonstrate two multiplex panels, including one for detection of 47 EGFR variants. ASPYRE presents an effective and accessible method that simplifies highly sensitive and multiplexed detection of somatic variants.
在肿瘤学的临床决策中,准确检测野生型背景下的体细胞变异至关重要。现有的方法,如等位基因特异性实时 PCR,通常仅限于单个靶基因,并且缺乏灵敏度。另一方面,下一代测序方法的检测周转时间长、成本高,且实施复杂,通常限制它们只能在单个地点使用。在这里,我们报告了一种称为等位基因特异性焦磷酸解反应(ASPYRE)的方法,用于高灵敏度检测体细胞变异的面板。ASPYRE 具有简单的工作流程,并且与标准分子生物学试剂和实时 PCR 仪器兼容。我们表明,ASPYRE 具有单分子灵敏度,并且能够耐受从血浆和福尔马林固定石蜡包埋(FFPE)样本中提取的 DNA。我们还展示了两个多重面板,包括一个用于检测 47 个 EGFR 变体的面板。ASPYRE 提供了一种有效且易于使用的方法,简化了对体细胞变异的高度敏感和多重检测。