Zhao Jing, Zhao Jin-Yin, Chen Zhi-Xia, Zhong Wei, Li Long-Yun, Liu Li-Cheng, Hu Xiao-Xu, Chen Wei-Jun, Wang Meng-Zhao
Department of Respiratory Medicine, PUMC Hospital, CAMS and PUMC, Beijing 100730, China.
Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100029, China.
Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2016 Dec 20;38(6):643-649. doi: 10.3881/j.issn.1000-503X.2016.06.004.
Objective To establish a real-time quantitative reverse transcription polymerase chain reaction assay (qRT-PCR) for the rapid, sensitive, and specific detection of echinoderm microtubule associated protein like 4-anaplastic lymphoma kinase (EML4-ALK) fusion genes in non-small cell lung cancer. Methods The specific primers for the four variants of EML4-ALK fusion genes (V1, V2, V3a, and V3b) and Taqman fluorescence probes for the detection of the target sequences were carefully designed by the Primer Premier 5.0 software. Then, using pseudovirus containing EML4-ALK fusion genes variants (V1, V2, V3a, and V3b) as the study objects, we further analyzed the lower limit, sensitivity, and specificity of this method. Finally, 50 clinical samples, including 3 ALK-fluorescence in situ hybridization (FISH) positive specimens, were collected and used to detect EML4-ALK fusion genes using this method. Results The lower limit of this method for the detection of EML4-ALK fusion genes was 10 copies/μl if no interference of background RNA existed. Regarding the method's sensitivity, the detection resolution was as high as 1% and 0.5% in the background of 500 and 5000 copies/μl wild-type ALK gene, respectively. Regarding the method's specificity, no non-specific amplification was found when it was used to detect EML4-ALK fusion genes in leukocyte and plasma RNA samples from healthy volunteers. Among the 50 clinical samples, 47 ALK-FISH negative samples were also negative. Among 3 ALK-FISH positive samples, 2 cases were detected positive using this method, but another was not detected because of the failure of RNA extraction. Conclusion The proposed qRT-PCR assay for the detection of EML4-ALK fusion genes is rapid, simple, sensitive, and specific, which is deserved to be validated and widely used in clinical settings.
目的 建立一种实时定量逆转录聚合酶链反应检测方法(qRT-PCR),用于快速、灵敏且特异检测非小细胞肺癌中的棘皮动物微管相关蛋白样4-间变性淋巴瘤激酶(EML4-ALK)融合基因。方法 利用Primer Premier 5.0软件精心设计EML4-ALK融合基因4种变体(V1、V2、V3a和V3b)的特异性引物以及用于检测靶序列的Taqman荧光探针。然后,以含有EML4-ALK融合基因变体(V1、V2、V3a和V3b)的假病毒为研究对象,进一步分析该方法的检测下限、灵敏度和特异性。最后,收集50份临床样本,其中包括3份ALK荧光原位杂交(FISH)阳性标本,采用该方法检测EML4-ALK融合基因。结果 在无背景RNA干扰的情况下,该方法检测EML4-ALK融合基因的下限为10拷贝/μl。就该方法的灵敏度而言,在500拷贝/μl和5000拷贝/μl野生型ALK基因背景下,检测分辨率分别高达1%和0.5%。就该方法的特异性而言,用其检测健康志愿者白细胞和血浆RNA样本中的EML4-ALK融合基因时未发现非特异性扩增。在50份临床样本中,47份ALK-FISH阴性样本也为阴性。在3份ALK-FISH阳性样本中,2例采用该方法检测为阳性,但另1例因RNA提取失败未检测到。结论 所建立的用于检测EML4-ALK融合基因的qRT-PCR检测方法快速、简便、灵敏且特异,值得在临床中进行验证并广泛应用。