dc.contributor.author
Hanssen, Annkathrin
dc.contributor.author
Wagner, Jenny
dc.contributor.author
Gorges, Tobias M.
dc.contributor.author
Taenzer, Aline
dc.contributor.author
Uzunoglu, Faik G.
dc.contributor.author
Driemel, Christiane
dc.contributor.author
Stoecklein, Nikolas H.
dc.contributor.author
Knoefel, Wolfram T.
dc.contributor.author
Angenendt, Sebastian;
dc.contributor.author
Hauch, Siegfried
dc.contributor.author
Atanackovic, Djordje
dc.contributor.author
Loges, Sonja
dc.contributor.author
Riethdorf, Sabine
dc.contributor.author
Pantel, Klaus
dc.contributor.author
Wikman, Harriet
dc.date.accessioned
2018-06-08T03:20:37Z
dc.date.available
2016-11-01T09:32:16.083Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/14974
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-19162
dc.description.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.
en
dc.rights.uri
http://creativecommons.org/licenses/by/4.0/
dc.subject
Epithelial–mesenchymal transition
dc.subject
Non-small-cell lung cancer
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit
dc.title
Characterization of different CTC subpopulations in non-small cell lung cancer
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation
Scientific Reports. - 6 (2016), Artikel Nr. 28010
dcterms.bibliographicCitation.doi
10.1038/srep28010
dcterms.bibliographicCitation.url
http://www.nature.com/articles/srep28010
refubium.affiliation
Charité - Universitätsmedizin Berlin
de
refubium.mycore.fudocsId
FUDOCS_document_000000025636
refubium.note.author
Der Artikel wurde in einer reinen Open-Access-Zeitschrift publiziert.
refubium.resourceType.isindependentpub
no
refubium.mycore.derivateId
FUDOCS_derivate_000000007280
dcterms.accessRights.openaire
open access