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一种用于快速简便检测PIK3CA基因中四种常见热点密码子突变的SNaPshot检测法。

A SNaPshot assay for the rapid and simple detection of four common hotspot codon mutations in the PIK3CA gene.

作者信息

Hurst Carolyn D, Zuiverloon Tahlita C M, Hafner Christian, Zwarthoff Ellen C, Knowles Margaret A

机构信息

Cancer Research UK Clinical Centre, Leeds Institute of Molecular Medicine, St James's University Hospital, Leeds, UK.

出版信息

BMC Res Notes. 2009 Apr 29;2:66. doi: 10.1186/1756-0500-2-66.

Abstract

BACKGROUND

Activating mutations in the PIK3CA gene have been identified in a variety of human malignancies and are commonly detected in hotspot codons located in the helical and kinase domains in exons 9 and 20. Existing methodologies for the detection of PIK3CA mutations are time-consuming and/or expensive. In the present study we describe the first application of a PIK3CA SNaPshot assay to the screening of frequent mutations in these exons.

FINDINGS

A SNaPshot assay for the simultaneous detection of four frequent PIK3CA hotspot mutations (E542K, E545G, E545K and H1047R) has been developed and evaluated. The assay combines multiplex PCR amplification with a multiplex primer extension assay to allow targeted detection of all four mutations in one reaction. The method was tested using samples that had previously been analysed for mutations by high-resolution melting analysis and sequencing. All mutations detected were concordant and no false positive results were obtained. Sensitivity tests showed that the SNaPshot assay could detect mutant DNA when it represents 5-10% of the total DNA present. The application of the method to the analysis of DNAs extracted from formalin-fixed paraffin-embedded samples was also demonstrated.

CONCLUSION

The SNaPshot assay described here offers a fast, sensitive, inexpensive and specific approach to the analysis of frequent PIK3CA mutations in both fresh and archival patient samples.

摘要

背景

PIK3CA基因的激活突变已在多种人类恶性肿瘤中被鉴定出来,并且常见于外显子9和20中位于螺旋和激酶结构域的热点密码子中。现有的检测PIK3CA突变的方法既耗时又昂贵。在本研究中,我们描述了PIK3CA SNaPshot检测法首次应用于这些外显子中常见突变的筛查。

研究结果

已开发并评估了一种用于同时检测四种常见PIK3CA热点突变(E542K、E545G、E545K和H1047R)的SNaPshot检测法。该检测法将多重PCR扩增与多重引物延伸检测相结合,以便在一个反应中靶向检测所有四种突变。使用先前通过高分辨率熔解分析和测序分析过突变的样本对该方法进行了测试。所有检测到的突变结果一致,未获得假阳性结果。敏感性测试表明,当突变型DNA占总DNA的5%-10%时,SNaPshot检测法能够检测到它。还展示了该方法在分析从福尔马林固定石蜡包埋样本中提取的DNA中的应用。

结论

本文所述的SNaPshot检测法为分析新鲜和存档患者样本中常见的PIK3CA突变提供了一种快速、灵敏、廉价且特异的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5af8/2683860/5eb904572ae3/1756-0500-2-66-1.jpg

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