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首页> 外文期刊>The Journal of molecular diagnostics: JMD >A PIK3CA pyrosequencing-based assay that excludes pseudogene interference
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A PIK3CA pyrosequencing-based assay that excludes pseudogene interference

机译:基于PIK3CA焦磷酸测序的检测方法,排除假基因干扰

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Phosphatidylinositol 3′-kinase gene (PIK3CA) encodes a lipid kinase that regulates signaling pathways downstream of epidermal growth factor receptor and is mutated in 10% to 30% of colorectal cancers. Activating mutations in this gene up-regulates the AKT signaling pathway, making it a potentially useful therapeutic target. Mutations in PIK3CA are not exclusive of mutations in KRAS, BRAF, or NRAS. We designed a pyrosequencing assay to detect mutations in all three positions of codons 542 and 545 in exon 9 and codon 1047 in exon 20 of this gene. The exon 9 reverse PCR primer was designed to avoid amplifying a pseudogene in chromosome 22 that has >95% homology with exons 9 through 13 in PIK3CA. Two hundred colorectal cancers from FFPE tissue previously characterized for KRAS mutation status were evaluated for PIK3CA mutations. In KRAS-mutated samples, 20% had an additional mutation in PIK3CA. The mutation rate in KRAS wild-type samples was 7.5%. When using our assay, pseudogene was not observed in any of these samples. In addition, pseudogene- and gene-specific amplification was performed on DNA from 40 additional colorectal cancers. Sequencing of these PCR products yielded the expected gene or pseudogene sequence in all cases. Thus, we have developed a PIK3CA pyrosequencing assay capable of detecting mutations in all three positions in the three hot spot codons with no pseudogene interference.
机译:磷脂酰肌醇3'激酶基因(PIK3CA)编码调节表皮生长因子受体下游信号通路的脂质激酶,并在10%至30%的大肠癌中发生突变。该基因中的激活突变上调AKT信号通路,使其成为潜在有用的治疗靶标。 PIK3CA中的突变并不排除KRAS,BRAF或NRAS中的突变。我们设计了焦磷酸测序测定法,以检测该基因第9外显子的542和545密码子和第20外显子的1047密码子的所有三个位置的突变。设计第9外显子反向PCR引物,以避免扩增第22号染色体上的假基因,该假基因与PIK3CA中第9至13外显子具有> 95%的同源性。对先前表征为KRAS突变状态的FFPE组织中的200例结直肠癌的PIK3CA突变进行了评估。在KRAS突变的样本中,有20%的PIK3CA有其他突变。 KRAS野生型样品中的突变率为7.5%。当使用我们的测定法时,在任何这些样品中均未观察到假基因。另外,对来自另外40种结直肠癌的DNA进行了假基因和基因特异性扩增。这些PCR产物的测序在所有情况下均产生了预期的基因或假基因序列。因此,我们开发了一种PIK3CA焦磷酸测序测定法,该测定法能够检测三个热点密码子中所有三个位置的突变而没有假基因干扰。

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