Characterization of different CTC subpopulations in non-small cell lung cancer

Annkathrin Hanssen(Universität Hamburg), Jenny Wagner, Tobias M. Gorges(Universität Hamburg), Aline Taenzer(Universität Hamburg), Faik G. Uzunoǧlu(Universität Hamburg), Christiane Driemel(Düsseldorf University Hospital), Nikolas H. Stoecklein(Düsseldorf University Hospital), Wolfram Trudo Knoefel(Düsseldorf University Hospital), Sebastian Angenendt(Düsseldorf University Hospital), Siegfried Hauch, Djordje Atanackovic(Universität Hamburg), Sonja Loges(Universität Hamburg), Sabine Riethdorf(Universität Hamburg), Klaus Pantel(Universität Hamburg), Harriet Wikman(Universität Hamburg)
Scientific Reports
June 15, 2016
Cited by 113Open Access
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Abstract

Circulating tumour cells (CTCs) serve as valuable biomarkers. However, EpCAM positive CTCs are less frequently detected in NSCLC patients compared to other epithelial tumours. First, EpCAM protein expression was analysed in primary and metastatic lung cancer tissue. In both groups 21% of the samples were EpCAM negative. Second, the CellSearch system identified 15% of patients (n = 48) as CTC positive whereas a multiplex RT-PCR for PIK3CA, AKT2, TWIST, and ALDH1 following EGFR, HER2 and EpCAM based enrichment detected CTCs in 29% of the patients. Interestingly, 86% of CTC positive patients were found to express ALDH1. Only 11% of the patients were CTC-positive by both techniques. CTC positivity was associated with patient disease state when assessed by the multiplex RT-PCR assay (p = 0.015). Patients harbouring tumours with an altered EGFR genotype were more frequently CTC-positive compared to patients with EGFR wildtype tumours. In subsets of patients, CTCs were found to express genes involved in resistance to therapy such as HER3 and MET. In conclusion, using multiple targets for CTC capture and identification increases the sensitivity of CTC detection in NSCLC patients, which can be explained by the presence of different CTC subtypes with distinct molecular features.


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