You Juneseok, Park Chanho, Jang Kuewhan, Park Jinsung, Na Sungsoo
Department of Mechanical Engineering, Korea University, Seoul 02841, Korea.
Division of Foundry, Samsung Electronics, Hwaseong-si 18448, Korea.
Materials (Basel). 2022 May 5;15(9):3301. doi: 10.3390/ma15093301.
The detection of circulating tumor DNA is a major challenge in liquid biopsies for cancer. Conventionally, quantitative polymerase chain reactions or next-generation sequencing are used to detect circulating tumor DNA; however, these techniques require significant expertise, and are expensive. Owing to the increasing demand for a simple diagnostic method and constant monitoring of cancer, a cost-effective detection technique that can be conducted by non-experts is required. The aim of this study was to detect the circulating tumor DNA containing the epidermal growth factor receptor (EGFR) exon 19 deletion, which frequently occurs in lung cancer. By applying walker DNA to a catalytic hairpin assembly and using the differential dispersibility of gold nanoparticles, we detected EGFR exon 19 deletion mutant #2 DNA associated with lung cancer. Our sensing platform exhibited a limit of detection of 38.5 aM and a selectivity of 0.1% for EGFR exon 19 wild-type DNA. Moreover, we tested and compared EGFR exon 19 deletion mutants #1 and #3 to evaluate the effect of base pair mismatches on the performance of the said technique.
循环肿瘤DNA的检测是癌症液体活检中的一项重大挑战。传统上,定量聚合酶链反应或下一代测序用于检测循环肿瘤DNA;然而,这些技术需要专业知识,且成本高昂。由于对简单诊断方法的需求不断增加以及对癌症的持续监测,需要一种非专业人员也能进行的经济高效的检测技术。本研究的目的是检测含有表皮生长因子受体(EGFR)外显子19缺失的循环肿瘤DNA,这种缺失在肺癌中经常出现。通过将沃克DNA应用于催化发夹组装,并利用金纳米颗粒的差异分散性,我们检测到了与肺癌相关的EGFR外显子19缺失突变体#2 DNA。我们的传感平台对EGFR外显子19野生型DNA的检测限为38.5 aM,选择性为0.1%。此外,我们测试并比较了EGFR外显子19缺失突变体#1和#3,以评估碱基对错配对上述技术性能的影响。