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ABSTRACT: Background
Here, we monitored the evolution of CTCs spread in 11 patients affected by locally advanced EC who were undergoing therapy.Methods
In this perspective study, we designed multiple blood biopsies from individual patients: before and after neoadjuvant chemo-radio therapy and after surgery. We developed a multi-target array, named Grab-all assay, to estimate CTCs for their epithelial (EpCAM/E-Cadherin/Cytokeratins) and mesenchymal/stem (N-Cadherin/CD44v6/ABCG2) phenotypes. Identified CTCs were isolated as single cells by DEPArray, subjected to whole genome amplification, and copy number aberration (CNA) profiles were determined. Through bioinformatic analysis, we assessed the genomic imbalance of single CTCs, investigated specific focal copy number changes previously
SUBMITTER: Gallerani G
PROVIDER: S-EPMC8699413 | biostudies-literature | 2021 Dec
REPOSITORIES: biostudies-literature