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用于诊断常规监测的数字液滴PCR:准备好开始了吗?

Droplet Digital PCR for Monitoring in Diagnostic Routine: Ready to Start?

作者信息

Bochicchio Maria Teresa, Petiti Jessica, Berchialla Paola, Izzo Barbara, Giugliano Emilia, Ottaviani Emanuela, Errichiello Santa, Rege-Cambrin Giovanna, Venturi Claudia, Luciano Luigiana, Daraio Filomena, Calistri Daniele, Rosti Gianantonio, Saglio Giuseppe, Martinelli Giovanni, Pane Fabrizio, Cilloni Daniela, Gottardi Enrico M, Fava Carmen

机构信息

Biosciences Laboratory, IRCCS Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST) "Dino Amadori", 47014 Meldola, Italy.

Department of Clinical and Biological Sciences, University of Turin, AOU San Luigi Gonzaga, Orbassano, 10043 Turin, Italy.

出版信息

Cancers (Basel). 2021 Oct 30;13(21):5470. doi: 10.3390/cancers13215470.

Abstract

mRNA levels represent the key molecular marker for the evaluation of minimal residual disease (MRD) in chronic myeloid leukemia (CML) patients and real-time quantitative PCR (RT-qPCR) is currently the standard method to monitor it. In the era of tyrosine kinase inhibitors (TKIs) discontinuation, droplet digital PCR (ddPCR) has emerged to provide a more precise detection of MRD. To hypothesize the use of ddPCR in clinical practice, we designed a multicentric study to evaluate the potential value of ddPCR in the diagnostic routine. Thirty-seven RNA samples from CML patients and five from healthy donors were analyzed using both ddPCR QXDx %IS Kit and LabNet-approved RT-qPCR methodologies in three different Italian laboratories. Our results show that ddPCR has a good agreement with RT-qPCR, but it is more precise to quantify transcript levels. Furthermore, we did not find differences between duplicate or quadruplicate analysis in terms of % IS values. Droplet digital PCR could be confidently introduced into the diagnostic routine as a complement to the RT-qPCR.

摘要

信使核糖核酸(mRNA)水平是评估慢性髓性白血病(CML)患者微小残留病(MRD)的关键分子标志物,实时定量聚合酶链反应(RT-qPCR)是目前监测MRD的标准方法。在酪氨酸激酶抑制剂(TKIs)停药时代,液滴数字聚合酶链反应(ddPCR)已出现,可更精确地检测MRD。为设想ddPCR在临床实践中的应用,我们设计了一项多中心研究,以评估ddPCR在诊断常规中的潜在价值。在意大利的三个不同实验室,使用ddPCR QXDx %IS试剂盒和经LabNet批准的RT-qPCR方法,对37份CML患者的RNA样本和5份健康供体的RNA样本进行了分析。我们的结果表明,ddPCR与RT-qPCR具有良好的一致性,但在定量转录本水平方面更精确。此外,就%IS值而言,我们在重复或四重分析之间未发现差异。液滴数字聚合酶链反应可作为RT-qPCR的补充,自信地引入诊断常规。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b909/8582412/513bd3027f76/cancers-13-05470-g001.jpg

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