alexa The Role of the Carcinoembryonic Antigen Receptor in Colorectal Cancer Progression
ISSN: 2329-6771

Journal of Integrative Oncology
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Research Article

The Role of the Carcinoembryonic Antigen Receptor in Colorectal Cancer Progression

Olga Bajenova1,2, Elena Tolkunova3, Sergey Koshkin3, Sergey Malov1, Peter Thomas4, Alexey Tomilin3 and Stephen O’Brien1

1Theodosius Dobzhansky Center for Genome Bioinformatics at St. Petersburg State University, St. Petersburg, Russia

2Department of Genetics and Biotechnology, St. Petersburg State University, St. Petersburg, Russia

3Institute of Cytology, Russian Academy of Sciences, St. Petersburg, Russia

4Department of Surgery, Creighton University, Omaha, USA

*Corresponding Author:
Olga Bajenova
Theodosius Dobzhansky Center for Genome Bioinformatics at St. Petersburg State University
41-43 Sredniy Prospekt, St Petersburg, Russia
Tel: +7-812-363-6103
E-mail: [email protected]

Received Date: March 25, 2017; Accepted Date: April 18, 2017; Published Date: April 28, 2017

Citation: Bajenova O, Tolkunova E, Koshkin S, Malov S, Thomas P, et al. (2017) The Role of the Carcinoembryonic Antigen Receptor in Colorectal Cancer Progression. J Integr Oncol 6:192. doi: 10.4172/2329-6771.1000192

Copyright: © 2017 Bajenova O, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

 

Abstract

Clinical and experimental data suggest that carcinoembryonic antigen (CEA, CD66e, CEACAM-5) plays a key role in the formation of hepatic metastasis from colorectal and other types of epithelial cancers. The molecular events involved in CEA-induced metastasis have yet to be defined. Our group first cloned the gene (CEAR) for CEA-binding protein from the surface of fixed liver macrophages, (Kupffer cells). In this study to further elucidate the role of CEAR in colorectal cancer progression, its expression in colorectal cancer cells was suppressed by short hairpin RNAs (shRNAs) in CEA-overexpressing and CEA - negative MIP-101 colorectal cancer cell lines. The data show that targeted suppression of endogenous CEAR in tumor cells resulted in changes in cell invasiveness. RT-PCR data indicated reduced levels of E-cadherin, Snail, MMP-2, and Oct-4 in the clones with suppressed CEAR suggesting a role in the epithelial mesenchymal transition. The comparative analysis of tumorigenic activity to the liver of the cell lines with suppressed CEAR has also been conducted using an intrasplenic injection model in immuno-deficient mice. This data shows a decrease in tumor progression associated with CEAR suppression. In summary the results of this study revealed a novel role for CEAR gene in the regulation of colorectal cancer cell invasiveness and progression.

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