TY - JOUR
T1 - Detection of circulating tumour cells with a hybrid (epithelial/ mesenchymal) phenotype in patients with metastatic non-small cell lung cancer
AU - Lecharpentier, A.
AU - Vielh, P.
AU - Perez-Moreno, P.
AU - Planchard, D.
AU - Soria, J. C.
AU - Farace, F.
PY - 2011/10/25
Y1 - 2011/10/25
N2 - Methods: CTCs were enriched by blood filtration using ISET (isolation by size of epithelial tumour cells), triply labelled with fluorescent anti-vimentin, anti-pan-keratin antibodies and SYTOX orange nuclear dye, and examined by confocal microscopy in six patients with metastatic non-small cell lung cancer (NSCLC). In parallel, CTCs were morphocytologically identified by an experienced cytopathologist. Results: Isolated or clusters of dual CTCs strongly co-expressing vimentin and keratin were evidenced in all patients (range 5-88/5 ml). CTCs expressing only vimentin were detected in three patients, but were less frequent (range 3-15/5 ml). No CTC expressing only keratin was detected. Conclusion: We showed for the first time the existence of hybrid CTCs with an epithelial/mesenchymal phenotype in patients with NSCLC. Their characterisation should provide further insight on the significance of EMT in CTCs and on the mechanism of metastasis in patients with NSCLC.
AB - Methods: CTCs were enriched by blood filtration using ISET (isolation by size of epithelial tumour cells), triply labelled with fluorescent anti-vimentin, anti-pan-keratin antibodies and SYTOX orange nuclear dye, and examined by confocal microscopy in six patients with metastatic non-small cell lung cancer (NSCLC). In parallel, CTCs were morphocytologically identified by an experienced cytopathologist. Results: Isolated or clusters of dual CTCs strongly co-expressing vimentin and keratin were evidenced in all patients (range 5-88/5 ml). CTCs expressing only vimentin were detected in three patients, but were less frequent (range 3-15/5 ml). No CTC expressing only keratin was detected. Conclusion: We showed for the first time the existence of hybrid CTCs with an epithelial/mesenchymal phenotype in patients with NSCLC. Their characterisation should provide further insight on the significance of EMT in CTCs and on the mechanism of metastasis in patients with NSCLC.
KW - ISET
KW - circulating tumour cells
KW - epithelial-mesenchymal transition
KW - metastasis
KW - metastatic non-small cell lung cancer
UR - http://www.scopus.com/inward/record.url?scp=80055001749&partnerID=8YFLogxK
U2 - 10.1038/bjc.2011.405
DO - 10.1038/bjc.2011.405
M3 - Article
C2 - 21970878
AN - SCOPUS:80055001749
SN - 0007-0920
VL - 105
SP - 1338
EP - 1341
JO - British Journal of Cancer
JF - British Journal of Cancer
IS - 9
ER -