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首页> 外文期刊>Applied immunohistochemistry and molecular morphology: AIMM >Sensitive Genotyping of Somatic Mutations in the EGFR, KRAS, PIK3CA, BRAF Genes from NSCLC Patients Using Hydrogel Biochips
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Sensitive Genotyping of Somatic Mutations in the EGFR, KRAS, PIK3CA, BRAF Genes from NSCLC Patients Using Hydrogel Biochips

机译:使用水凝胶生物芯片对来自NSCLC患者的EGFR,KRAS,PIK3CA,BRAF基因的体细胞突变进行敏感基因分型

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摘要

Targeted inhibitors of the epidermal growth factor receptor (EGFR) are used for the treatment of non-small cell lung cancer (NSCLC). Somatic mutations in the EGFR gene and key effectors of the EGFR-signaling pathway (KRAS, BRAF, PIK3CA) are associated with sensitivity to these drugs. We developed a highly sensitive LUNG CANCER (LC)-biochip approach for the detection of the most common EGFR, KRAS, PIK3CA, and BRAF gene mutations. The locked nucleic acid clamp PCR technique was used to increase the sensitivity of the assay, then allele-specific hybridization of a fluorescently labeled target on a biochip was performed. To prove the feasibility of the approach, clinical samples from 112 patients with NSCLC were analyzed.
机译:表皮生长因子受体(EGFR)的靶向抑制剂用于治疗非小细胞肺癌(NSCLC)。 EGFR基因的体细胞突变和EGFR信号通路的关键效应子(KRAS,BRAF,PIK3CA)与对这些药物的敏感性有关。我们开发了一种高度灵敏的肺癌(LC)生物芯片方法,用于检测最常见的EGFR,KRAS,PIK3CA和BRAF基因突变。使用锁定的核酸钳PCR技术来增加测定的灵敏度,然后对生物芯片上的荧光标记靶标进行等位基因特异性杂交。为了证明该方法的可行性,对112例NSCLC患者的临床样本进行了分析。

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