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ABSTRACT: Background
MYC (v-myc avian myelocytomatosis viral oncogene homolog) is one of the most frequently amplified genes in lung tumors. For the analysis of gene copy number variations, dPCR (digital PCR) is an appropriate tool. The aim of our study was the assessment of dPCR for the detection of MYC copy number variations (CNV) in lung tissue considering clinicopathological parameters. Material and Methods. MYC status was analyzed with dPCR as well as qPCR (quantitative PCR) using gDNA (genomic DNA) from tumor and adjacent nontumor tissue samples of lung cancer patients. The performance of MYC was estimated based on the AUC (area under curve).Results
The results of the MYC amplification correlated significantly between dPCR and qPCR (
SUBMITTER: Brik A
PROVIDER: S-EPMC7525309 | biostudies-literature | 2020
REPOSITORIES: biostudies-literature