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Rapid detection of epidermal growth factor receptor mutations with multiplex PCR and primer extension in lung cancer

机译:多重PCR和引物延伸快速检测肺癌中的表皮生长因子受体突变

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Epidermal growth factor receptor (EGFR) kinase domain mutations hyperactivate the kinase and confer kinase addiction of the non-small-cell lung cancer (NSCLC) tumor cells. Almost all of these mutations are located within exons 18-21. The -216 single nucleotide polymorphism in the promoter region is associated with increased EGFR production. We present a method for detecting these common mutations in 81 cases of NSCLC. The protocol is based on the multiplex amplification of promoter region and exons 18-21 of the EGFR genes in a single tube, followed by primer extension of the PCR products using various sizes of primers to detect base changes at -216 promoter region and codons 719, 746-750, 790, 858 of the EGFR gene. We compared the results with that from direct sequencing for detecting EGFR mutations in 81 cases of NSCLC. The two methods identified the same 26 mutations, but our method is superior to direct sequencing in terms of the amount of work and time required. We presented a simple and fast method to detect mutations of EGFR genes in NSCLC.
机译:表皮生长因子受体(EGFR)激酶结构域突变使非小细胞肺癌(NSCLC)肿瘤细胞激活该激酶并赋予激酶成瘾性。几乎所有这些突变都位于外显子18-21内。启动子区域中的-216单核苷酸多态性与EGFR产生增加有关。我们提出了一种检测81例NSCLC患者常见突变的方法。该协议基于单个管中EGFR基因启动子区域和外显子18-21的多重扩增,然后使用各种大小的引物检测PCR产物的引物延伸,以检测-216启动子区域和719位密码子的碱基变化,EGFR基因的746-750、790、858。我们将结果与直接测序法检测81例NSCLC EGFR突变的结果进行了比较。两种方法可以识别出相同的26个突变,但就工作量和所需时间而言,我们的方法优于直接测序。我们提出了一种简单快速的方法来检测NSCLC中EGFR基因的突变。

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