微滴数字PCR分析肺腺癌患者上皮生长因子受体突变的游离DNA

Q4 Medicine
H. Faisal, Y. Horimasu, Shoko Hirano, E. Yamaoka, Takahiro Fukazawa, Masami Kanawa, K. Tanimoto, N. Hattori, N. Kohno, Yuka Ueda, T. Sueda, E. Hiyama
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引用次数: 3

摘要

无细胞DNA (cfDNA)分析可能为肺腺癌患者提供一种无创诊断方法。近年来,液滴数字PCR (ddPCR)作为一种高灵敏度的低突变等位基因检测方法得到了发展。使用细胞系评估上皮生长因子受体(EGFR)突变的ddPCR检测限,NCI-H1975检测EGFR L858R点突变,PC-9检测EGFR E746-A750del。随后,对19例肺腺癌患者的肿瘤DNA (tDNA)和cfDNA样本进行ddPCR检测EGFR突变,这些患者的肿瘤活检已经通过钳形PCR评估了EGFR突变(L858R 13例,E746-750del 3例,EGFR阴性3例)。对12例进行免疫组化分析,量化EGFR l858r阳性细胞数的比例。在16份肿瘤DNA样本中检测到EGFR点突变或缺失。在可测cfDNA样本中,L858R和E746A750del的cfDNA的ddPCR检出率分别为61.5%(8/13)和100%(3/3)。tDNA等位基因分数(AF)与EGFR l858r阳性细胞数呈相对相关。tDNA的心房颤动与cfDNA的心房颤动无相关性。在我们的研究中,cfDNA突变检测与临床病理特征无关,但cfDNA高AF的病例确实存在转移性病变。我们的研究表明,ddPCR能够对EGFR L858R和E746-A750del进行cfDNA分析,检出率高。因此,利用ddPCR分析cfDNA可作为肿瘤活检的补充,有利于肺腺癌患者的精准医疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cell-Free DNA Analysis of Epithelial Growth Factor Receptor Mutations in Lung Adenocarcinoma Patients by Droplet Digital PCR
Cell-free DNA (cfDNA) analysis may provide a non-invasive diagnostic approach for lung adenocarcinoma patients. Recently, droplet digital PCR (ddPCR) has been developed as a highly sensitive detection method for a low mutant allele percentage. The ddPCR detection limit for epithelial growth factor receptor (EGFR) mutations was evaluated using cell lines, NCI-H1975 for EGFR L858R point mutation and PC-9 for EGFR E746-A750del. Subsequently, detection of EGFR mutations by ddPCR was performed in tumor DNA (tDNA) and cfDNA samples of 19 lung adenocarcinoma patients whose tumor biopsies were already evaluated for EGFR mutations by clamp PCR (13 of L858R, 3 of E746-750del, and 3 of EGFR negative). In 12 cases, immunohistochemical analysis was performed to quantify the number of EGFR L858R-positive cells rate. EGFR point mutation or deletion were detected in 16 tumor DNA samples. In the measurable cfDNA samples, the rate of detection by ddPCR in cfDNA was 61.5% (8/13) for L858R and 100% (3/3) for E746A750del. A relative correlation was found between the allele fraction (AF) of tDNA and the number of EGFR L858R-positive cells rate. No correlation was found between the AF of tDNA and AF of cfDNA. In our study, cfDNA mutation detection was not associated with clinicopathological features, but cases with high AF of cfDNA did have metastatic lesions. Our study shows that ddPCR enables cfDNA analysis for EGFR L858R and E746-A750del, with a high detection rate. Therefore, cfDNA analysis using ddPCR may complement to tumor biopsy and is beneficial for precision medicine in lung adenocarcinoma patients.
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来源期刊
Hiroshima journal of medical sciences
Hiroshima journal of medical sciences Medicine-Medicine (all)
CiteScore
0.30
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