Your browser doesn't support javascript.
loading
CD44v6 Defines a New Population of Circulating Tumor Cells Not Expressing EpCAM.
Belthier, Guillaume; Homayed, Zeinab; Grillet, Fanny; Duperray, Christophe; Vendrell, Julie; Krol, Ilona; Bravo, Sophie; Boyer, Jean-Christophe; Villeronce, Olivia; Vitre-Boubaker, Jihane; Heaug-Wane, Diana; Macari-Fine, Françoise; Smith, Jai; Merlot, Matthieu; Lossaint, Gérald; Mazard, Thibault; Portales, Fabienne; Solassol, Jérôme; Ychou, Marc; Aceto, Nicola; Mamessier, Emilie; Bertucci, François; Pascussi, Jean Marc; Samalin, Emmanuelle; Hollande, Frédéric; Pannequin, Julie.
Afiliación
  • Belthier G; Institute of Functional Genomics (IGF), UMR5203 CNRS, U1191 INSERM and UM, 34094 Montpellier, France.
  • Homayed Z; Institute of Functional Genomics (IGF), UMR5203 CNRS, U1191 INSERM and UM, 34094 Montpellier, France.
  • Grillet F; Institute of Functional Genomics (IGF), UMR5203 CNRS, U1191 INSERM and UM, 34094 Montpellier, France.
  • Duperray C; Cytometry IRMB, Montpellier Rio Imaging, 34090 Montpellier, France.
  • Vendrell J; Department of Pathology and Onco-Biology, CHU Montpellier, 34295 Montpellier, France.
  • Krol I; Department of Biology, Institute of Molecular Health Sciences, ETH Zurich, 8093 Zurich, Switzerland.
  • Bravo S; Laboratoire de Biochimie, CHU Carémeau, 30900 Nîmes, France.
  • Boyer JC; Laboratoire de Biochimie, CHU Carémeau, 30900 Nîmes, France.
  • Villeronce O; Institute of Functional Genomics (IGF), UMR5203 CNRS, U1191 INSERM and UM, 34094 Montpellier, France.
  • Vitre-Boubaker J; Institute of Functional Genomics (IGF), UMR5203 CNRS, U1191 INSERM and UM, 34094 Montpellier, France.
  • Heaug-Wane D; Institute of Functional Genomics (IGF), UMR5203 CNRS, U1191 INSERM and UM, 34094 Montpellier, France.
  • Macari-Fine F; Institute of Functional Genomics (IGF), UMR5203 CNRS, U1191 INSERM and UM, 34094 Montpellier, France.
  • Smith J; Department of Clinical Pathology, Victorian Comprehensive Cancer Centre, The University of Melbourne, Melbourne, VIC 3010, Australia.
  • Merlot M; University of Melbourne Centre for Cancer Research, Victorian Comprehensive Cancer Centre, Melbourne, VIC 3010, Australia.
  • Lossaint G; Medical Oncology Department, Institut du Cancer de Montpellier (ICM), University Montpellier, 34298 Montpellier, France.
  • Mazard T; Medical Oncology Department, Institut du Cancer de Montpellier (ICM), University Montpellier, 34298 Montpellier, France.
  • Portales F; Medical Oncology Department, Institut du Cancer de Montpellier (ICM), University Montpellier, 34298 Montpellier, France.
  • Solassol J; Medical Oncology Department, Institut du Cancer de Montpellier (ICM), University Montpellier, 34298 Montpellier, France.
  • Ychou M; Department of Pathology and Onco-Biology, CHU Montpellier, 34295 Montpellier, France.
  • Aceto N; Montpellier Research Cancer Institute (IRCM), INSERM U1194, University of Montpellier, 34298 Montpellier, France.
  • Mamessier E; Medical Oncology Department, Institut du Cancer de Montpellier (ICM), University Montpellier, 34298 Montpellier, France.
  • Bertucci F; Department of Biology, Institute of Molecular Health Sciences, ETH Zurich, 8093 Zurich, Switzerland.
  • Pascussi JM; Predictive Oncology Laboratory, Cancer Research Center of Marseille (CRCM), Inserm U1068, CNRS UMR7258, Institut Paoli-Calmettes, Aix Marseille Université, 13009 Marseille, France.
  • Samalin E; Predictive Oncology Laboratory, Cancer Research Center of Marseille (CRCM), Inserm U1068, CNRS UMR7258, Institut Paoli-Calmettes, Aix Marseille Université, 13009 Marseille, France.
  • Hollande F; Institute of Functional Genomics (IGF), UMR5203 CNRS, U1191 INSERM and UM, 34094 Montpellier, France.
  • Pannequin J; Institute of Functional Genomics (IGF), UMR5203 CNRS, U1191 INSERM and UM, 34094 Montpellier, France.
Cancers (Basel) ; 13(19)2021 Oct 02.
Article en En | MEDLINE | ID: mdl-34638450
ABSTRACT
Circulating tumor cells (CTCs) are promising diagnostic and prognostic tools for clinical use. In several cancers, including colorectal and breast, the CTC load has been associated with a therapeutic response as well as progression-free and overall survival. However, counting and isolating CTCs remains sub-optimal because they are currently largely identified by epithelial markers such as EpCAM. New, complementary CTC surface markers are therefore urgently needed. We previously demonstrated that a splice variant of CD44, CD44 variable alternative exon 6 (CD44v6), is highly and specifically expressed by CTC cell lines derived from blood samples in colorectal cancer (CRC) patients. Two different approaches-immune detection coupled with magnetic beads and fluorescence-activated cell sorting-were optimized to purify CTCs from patient blood samples based on high expressions of CD44v6. We revealed the potential of the CD44v6 as a complementary marker to EpCAM to detect and purify CTCs in colorectal cancer blood samples. Furthermore, this marker is not restricted to colorectal cancer since CD44v6 is also expressed on CTCs from breast cancer patients. Overall, these results strongly suggest that CD44v6 could be useful to enumerate and purify CTCs from cancers of different origins, paving the way to more efficacious combined markers that encompass CTC heterogeneity.
Palabras clave

Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Año: 2021 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Año: 2021 Tipo del documento: Article