| Literature DB >> 17251334 |
Elizabeth C Wolstencroft1, Katy Hanlon, Lorna W Harries, Graham R Standen, Alexander Sternberg, Sian Ellard.
Abstract
Achieving a specific diagnosis of polycythemia vera (PV) and other myeloproliferative disorders (MPDs) is often costly and complex. However, the recent identification of a V617F mutation in the JH2 domain of the JAK2 gene in a high proportion of patients suffering from MPDs may provide confirmation of a diagnosis. This is an acquired mutation and, as such, may only be present in a small number of cells within a sample. There is therefore a clinical need for highly sensitive detection techniques. We have developed a sensitive real-time polymerase chain reaction (PCR)-based approach for both detection and quantification of the JAK2 V671F mutation load, which allows determination of mutation status without the need for prior purification of granulocytes. We have performed a comparison of this assay with two previously published detection methods. Although an amplification refractory mutation system (ARMS) was shown to be slightly superior in terms of sensitivity, our real-time PCR method provides the potential for quantification of the JAK2 V617F mutation, having potential future applications in the monitoring of minimal residual disease or predicting outcome of disease severity.Entities:
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Year: 2007 PMID: 17251334 PMCID: PMC1867420 DOI: 10.2353/jmoldx.2007.060083
Source DB: PubMed Journal: J Mol Diagn ISSN: 1525-1578 Impact factor: 5.568