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A sensitive and reliable semi-quantitative real-time PCR assay to detect JAK2 V617F in blood.

机译:一种灵敏可靠的半定量实时PCR检测试剂盒,可检测血液中的JAK2 V617F。

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摘要

Diagnosis of the myeloproliferative disorders, polycythemia vera (PV), essential thrombocythemia (ET) and idiopathic myelofibrosis (IMF) is difficult due to lack of diagnostic markers. Recently, the acquisition of a mutation in the Janus kinase 2 (JAK2) gene by hemopoietic cells has been described as a genetic defect underlying myeloproliferative disorders. The mutation leads to constitutive activation of JAK2, a tyrosine kinase involved in cytokine receptor signalling. Because of the clinical importance of this mutation (JAK2 V617F) in diagnosing myeloproliferative disorders and its relevance for disease progression, we developed a semi-quantitative real-time PCR test to detect JAK2 V617F. With this assay, quantities down to 0.8% JAK2 V617F amongst wild-type DNA could reliably be detected. For quantification purposes, low intra- and inter-assay variabilities ensure good reproducibility of the assay. Thus the JAK2 V617F qPCR assay described here is quick, robust, simple and more sensitive than direct sequencing, RFLP, ARMS assay and other methods published so far to detect JAK2 V617F. We therefore believe that the assay will contribute to early diagnosis of myeloproliferative disorders and to disease management, especially when JAK2-specific inhibitors have become available for therapeutic use.
机译:由于缺乏诊断标记,很难诊断骨髓增生异常,真性红细胞增多症(PV),原发性血小板增多症(ET)和特发性骨髓纤维化(IMF)。近来,造血细胞获得Janus激酶2(JAK2)基因突变已被描述为骨髓增生性疾病的遗传缺陷。该突变导致JAK2的组成性激活,JAK2是一种参与细胞因子受体信号传导的酪氨酸激酶。由于该突变(JAK2 V617F)在诊断骨髓增生性疾病中的临床重要性及其与疾病进展的相关性,我们开发了一种半定量实时PCR测试来检测JAK2 V617F。通过这种测定,可以可靠地检测到野生型DNA中低至0.8%JAK2 V617F的数量。出于定量目的,低的测定内和测定间变异性可确保测定的良好重现性。因此,此处描述的JAK2 V617F qPCR测定法比直接测序,RFLP,ARMS测定法和迄今已发布的其他方法来检测JAK2 V617F的方法更为快速,可靠,简单且敏感。因此,我们认为该测定将有助于骨髓增生异常的早期诊断和疾病的治疗,特别是当JAK2特异性抑制剂可用于治疗时。

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