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Analysis of KRAS Mutations of Exon 2 Codons 12 and 13 by SNaPshot Analysis in Comparison to Common DNA Sequencing

机译:通过SNaPshot分析与普通DNA测序比较分析外显子2密码子12和13的KRAS突变

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摘要

Due to the call for fast KRAS mutation status analysis for treatment of patients with monoclonal antibodies for metastatic colorectal cancer, sensitive, economic, and easily feasible methods are required. Under this aspect, the sensitivity and specificity of the SNaPshot analysis in comparison to the commonly used DNA sequencing was checked. We examined KRAS mutations in exon 2 codons 12 and 13 with DNA sequencing and SNaPshot analysis in 100 formalin-fixed paraffin-embedded tumor tissue samples of pancreatic carcinoma, colorectal carcinoma, and nonsmall cell lung cancer specimens of the primary tumor or metastases. 40% of these samples demonstrated mutated KRAS genes using sequencing and SNaPshot-analysis; additional five samples (45/100) were identified only with the SNaPshot. KRAS mutation detection is feasible with the reliable SNaPshot analysis method. The more frequent mutation detection by the SNaPshot analysis shows that this method has a high probability of accuracy in the detection of KRAS mutations compared to sequencing.
机译:由于呼吁使用单克隆抗体治疗转移性结直肠癌的患者进行快速KRAS突变状态分析,因此需要灵敏,经济且简便可行的方法。在这方面,检查了与常规DNA测序相比的SNaPshot分析的敏感性和特异性。我们用DNA测序和SNaPshot分析检查了100个福尔马林固定石蜡包埋的胰腺癌,大肠癌和非小细胞肺癌标本的原发性或转移性肿瘤标本中的2个密码子12和13的KRAS突变。这些样本中有40%通过测序和SNaPshot分析显示出KRAS基因突变;仅使用SNaPshot鉴定了另外五个样品(45/100)。可靠的SNaPshot分析方法可实现KRAS突变检测。通过SNaPshot分析进行的更频繁的突变检测表明,与测序相比,该方法在检测KRAS突变方面具有较高的准确性。

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