KRAS Codons 12 and 13 Mutation Analysis: A Comparative Study between Direct Sequencing and a New Sensitive Real-Time PCR Assay

S. Marzinotto, F. Sessa, A. Franzoni, A. Anselmi, L. Gastaldo, Silvia Mason, G. Damante, C. Beltrami, L. Mariuzzi
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引用次数: 4

Abstract

KRAS somatic mutations are found in 30–40% of colorectal cancer (CRC). Seven mutations in codons 12 and 13 of KRAS (95% of the observed human mutations) preclude the efficacy of anti-EGFR therapy for the treatment of CRC. Assessment of KRAS mutational status has become a standard procedure in the management of patients with CRC. Technically, KRAS mutation testing can be performed with different methods, characterized by distinct sensitivities and specificities. The present study analyzed KRAS in 182 CRC histological samples by using direct sequencing and a new kit based on a Real-Time Sequence-Specific Primers-PCR technology. The kit allowed to recover as positive 17 samples that were negative or unclear by sequencing, with a recovery rate equal to 13.82%. This study proposes a fast, sensitive, and high-throughput system to identify such seven described mutations of KRAS gene in CRC samples.
KRAS密码子12和13突变分析:直接测序与新型灵敏实时PCR的比较研究
在30-40%的结直肠癌(CRC)中发现KRAS体细胞突变。KRAS密码子12和13的7个突变(占观察到的人类突变的95%)排除了抗egfr治疗结直肠癌的疗效。KRAS突变状态的评估已成为CRC患者管理的标准程序。从技术上讲,KRAS突变检测可以用不同的方法进行,具有不同的敏感性和特异性。本研究采用直接测序和基于Real-Time sequence specific primer - pcr技术的新试剂盒对182份结直肠癌组织学样本的KRAS进行了分析。试剂盒对17份测序阴性或不明确的样品恢复为阳性,回收率为13.82%。本研究提出了一种快速、灵敏、高通量的系统来鉴定CRC样本中这七种KRAS基因突变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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