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Demasking of epithelial cell adhesion molecule (EpCAM) on circulating epithelial tumor cells by Tween®20 treatment in breast cancer patients

  • Katya Hekimian EMAIL logo , Ernst-Ludwig Stein , Ulrich Pachmann and Katharina Pachmann
Published/Copyright: December 7, 2012

Abstract

Background: The epithelial cell adhesion molecule (EpCAM) embedded in the plasma membrane of circulating epithelial tumor cells (CETC) is used for detection and enrichment of circulating tumor cells in peripheral blood and as a target for anti-epithelial antibodies elicited during immune response in anti-tumor immunization. Although an efficient immune response against EpCAM can be generated, the clinical application of such approaches has not been successful so far and the detection of circulating epithelial cells is highly variable. One reason for these discrepancies may be that not all circulating tumor cells are equally accessible for the specific antibody. A possible reason might be masking of EpCAM by glycoproteins or membrane lipoproteins preventing antibody binding.

Methods: We have tested the application of detergents as demasking agents known to be successful in demasking red blood cell epitopes and determined how and in which way they affect integral membrane proteins and membrane lipids.

Results: The results showed that the polysorbate Tween®20, a non-ionic detergent like organic solvent is able to demask EpCAM on CETC and makes it better accessible to its specific antibody retaining at the same time full cell viability.

Conclusions: The data presented in this study suggest that EpCAM is present on part of circulating tumor cells in a masked form and that it is possible to demask EpCAM on CETC of breast cancer patients using Tween®20 treatment. But further studies are needed to elucidate the mechanism of demasking.


Corresponding author: Katya Hekimian, Clinic for Internal Medicine II, Oncology Research Laboratory, Friedrich Schiller University Jena, Erlanger Allee 101, 07740 Jena, Germany Phone: +49 3641 9325821, Fax: +49 3641 9325827

Received: 2011-7-11
Accepted: 2011-11-15
Published Online: 2012-12-7
Published in Print: 2012-04-01

©2012 by Walter de Gruyter Berlin Boston

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