AI Article Synopsis

  • - This study addresses the challenge of detecting rare mutations in the EGFR gene from circulating tumor DNA (ctDNA) in lung cancer, due to interference from excess normal DNA.
  • - Researchers developed a droplet digital PCR (ddPCR) platform using a PDMS chip and double-layer glass reservoir, which efficiently creates and protects tiny droplets necessary for accurate mutation detection.
  • - The device demonstrated high sensitivity, successfully identifying the rare EGFR L858R mutation even in samples with a high background of wild-type DNA, and was validated on lung cancer patient samples.

Article Abstract

The lack of reliable and practical method for detecting rare hot mutation of epidermal growth factor receptor (EGFR) in circulating tumor DNA (ctDNA) for lung cancer has remained a challenge for general clinical application due to excess wild type DNA in clinical samples. In this study, we developed a droplet digital PCR (ddPCR) platform, integrating a PDMS chip and double-layer glass reservoir. The duplex T-junction droplet generators in PDMS chip can produce about one million uniform droplets of 4.187 pL within ∼10 min, which were then stored in the glass reservoir. The double-layer glass reservoir can protect droplets from evaporation and breaking, solving the problem of instability during thermal-cycling. The quantitative capabilities of the ddPCR chip were evaluated by testing EGFR exon gene 21, with a good linear correlation in the wide range of 10 to 10 copies/μL (R = 0.9998). We then demonstrated that the proposed ddPCR device can recognize rare EGFR L858R mutation under a background of 10 copies/μL wild-type DNA at a sensitivity of 0.0001%. Finally, we demonstrated this ddPCR platform could identify low amount of EGFR L858R mutation in ctDNA and CTCs of patients with lung cancer.

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http://dx.doi.org/10.1016/j.ab.2022.114877DOI Listing

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