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首页> 外文期刊>Clinical and experimental medicine >Rapid and sensitive allele-specific (AS)-RT-PCR assay for detection of T315I mutation in chronic myeloid leukemia patients treated with tyrosine-kinase inhibitors.
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Rapid and sensitive allele-specific (AS)-RT-PCR assay for detection of T315I mutation in chronic myeloid leukemia patients treated with tyrosine-kinase inhibitors.

机译:快速和敏感的等位基因特异性(AS)-RT-PCR检测,用于检测酪氨酸激酶抑制剂治疗的慢性粒细胞白血病患者中的T315I突变。

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摘要

Point mutations in the kinase domain of BCR-ABL were described in 40-90% of patients with chronic myeloid leukemia (CML) resistant to Imatinib. We herein describe the development of a rapid allele-specific (AS)-RT-PCR assay to identify the T315I mutation, which confers full resistance to all available tyrosine-kinase inhibitors (TKI). The mutation status of 65 patients with resistant CML was evaluated, and the T315I was detected in 3/65 (4.6%). Comparisons between sequencing and AS-RT-PCR results, as well as serial dilutions experiments proved that the method is specific and reproducible, with maximum sensitivity of 1 x 10(-3). The developed assay is a convenient and easy tool to be used in research of CML resistance for rapid mutation screening and, together with sequencing, may be included in efficient strategies for early detection of TKI resistance in patients with CML.
机译:在40-90%的对伊马替尼有抗药性的慢性粒细胞白血病(CML)患者中,描述了BCR-ABL激酶结构域中的点突变。我们在本文中描述了快速等位基因特异性(AS)-RT-PCR测定法的发展,以鉴定T315I突变,该突变赋予对所有可用酪氨酸激酶抑制剂(TKI)的完全抗性。对65例CML耐药患者的突变状态进行了评估,并且T315I的检出率为3/65(4.6%)。测序和AS-RT-PCR结果之间的比较以及连续稀释实验证明,该方法具有特异性和可重复性,最大灵敏度为1 x 10(-3)。这项开发的检测方法是一种方便,易用的工具,可用于研究CML耐药性以进行快速突变筛查,并且与测序一起可纳入CML患者早期检测TKI耐药性的有效策略中。

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