| Literature DB >> 34954118 |
Diana Y Vargas1, Sanjay Tyagi1, Salvatore A E Marras1, Patricia Moerzinger2, Juan A Abin-Carriquiry2, Mauricio Cuello3, Clara Rodriguez3, Andrés Martinez4, Alex Makhnin4, Andrea Farina4, Chintan Patel4, Tuan L Chuang4, Bob T Li5, Fred R Kramer6.
Abstract
SuperSelective primers, by virtue of their unique design, enable the simultaneous identification and quantitation of inherited reference genes and rare somatic mutations in routine multiplex PCR assays, while virtually eliminating signals from abundant wild-type sequences closely related to the target mutations. These assays are sensitive, specific, rapid, and low cost, and can be performed in widely available spectrofluorometric thermal cyclers. Herein, we provide examples of SuperSelective PCR assays that target eight different somatic EGFR mutations, irrespective of whether they occur in the same codon, occur at separate sites within the same exon, or involve deletions. In addition, we provide examples of SuperSelective PCR assays that detect specific EGFR mutations in circulating tumor DNA present in the plasma of liquid biopsies obtained from patients with non-small-cell lung cancer. The results suggest that multiplex SuperSelective PCR assays may enable the choice, and subsequent modification, of effective targeted therapies for the treatment of an individual's cancer, utilizing frequent noninvasive liquid biopsies.Entities:
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Year: 2021 PMID: 34954118 PMCID: PMC8961470 DOI: 10.1016/j.jmoldx.2021.11.006
Source DB: PubMed Journal: J Mol Diagn ISSN: 1525-1578 Impact factor: 5.568