Sakai Kazuko, Yoneshige Azusa, Ito Akihiko, Ueda Yoji, Kondo Satoshi, Nobumasa Hitoshi, Fujita Yoshihiko, Togashi Yosuke, Terashima Masato, De Velasco Marco A, Tomida Shuta, Nishio Kazuto
Department of Genome Biology, Kinki University Faculty of Medicine, Osaka-Sayama, Osaka, Japan.
Department of Pathology, Kinki University Faculty of Medicine, Osaka-Sayama, Osaka, Japan.
Springerplus. 2015 Jan 5;4(1):7. doi: 10.1186/2193-1801-4-7. eCollection 2015.
We compared the performance of the 3D-Gene® mutation assay (3D-Gene® KRAS mutation assay kit) with the Scorpion-ARMS (therascreen® KRAS RGQ PCR Kit) and Luminex (MEBGEN™ KRAS kit) assays for the detection of KRAS mutations in formalin-fixed, paraffin-embedded tissue samples from 150 patients diagnosed with colorectal cancer. DNA was extracted from the paraffin-embedded tissue samples with or without macrodissection under hematoxylin and eosin staining and the KRAS mutation status was independently determined using these assays. Discordant results were re-analyzed by Sanger sequencing. Mutation detection analysis was successfully performed in all 150 specimens using the 3D-Gene® mutation assay without an invalid case. The concordance rate between the 3D-Gene® mutation assay and Scorpion-ARMS or Luminex was 98.7% (148/150). KRAS mutations were detected at a frequency of 35.3% (53/150) in colorectal cancer specimens. Three discrepant cases were found between the three assays. Overall, our results demonstrate a high concordance rate of between the 3D-Gene® mutation assay and the two existing in-vitro diagnostics kits. All three assays proved to be validated methods for detecting clinically significant KRAS mutations in paraffin-embedded tissue samples.
我们比较了3D-Gene®突变检测法(3D-Gene® KRAS突变检测试剂盒)与蝎形扩增阻滞突变系统(therascreen® KRAS RGQ PCR试剂盒)以及Luminex(MEBGEN™ KRAS试剂盒)检测法,用于检测150例经诊断患有结直肠癌的患者福尔马林固定、石蜡包埋组织样本中的KRAS突变。在苏木精和伊红染色下,对石蜡包埋组织样本进行或不进行宏观解剖后提取DNA,并使用这些检测法独立确定KRAS突变状态。对不一致的结果通过桑格测序进行重新分析。使用3D-Gene®突变检测法在所有150个样本中均成功进行了突变检测分析,无无效病例。3D-Gene®突变检测法与蝎形扩增阻滞突变系统或Luminex之间的一致性率为98.7%(148/150)。在结直肠癌样本中,KRAS突变的检测频率为35.3%(53/150)。在这三种检测法之间发现了3例不一致的病例。总体而言,我们的结果表明3D-Gene®突变检测法与两种现有的体外诊断试剂盒之间具有较高的一致性率。所有这三种检测法都被证明是检测石蜡包埋组织样本中具有临床意义的KRAS突变的有效方法。