Carcinoembryonic antigen promotes colorectal cancer progression by targeting adherens junction complexes

被引:34
作者
Bajenova, Olga [1 ,2 ,3 ]
Chaika, Nina [3 ]
Tolkunova, Elena [4 ]
Davydov-Sinitsyn, Alexander [4 ]
Gapon, Svetlana [5 ]
Thomas, Peter [3 ]
O'Brien, Stephen [1 ]
机构
[1] St Petersburg State Univ, Theodosius Dobzhansky Ctr Genome Bioinformat, St Petersburg 199034, Russia
[2] St Petersburg State Univ, Dept Genet & Biotechnol, St Petersburg 199034, Russia
[3] Creighton Univ, Dept Surg & Biomed Sci, Omaha, NE 68178 USA
[4] Russian Acad Sci, Inst Cytol, St Petersburg 194064, Russia
[5] Boston Childrens Hosp, Boston, MA 02115 USA
关键词
Colorectal carcinoma; Carcinoembryonic antigen; Metastasis; CEAR; RNA binding protein; Adherens junction; E-cadherin; alpha-catenin; beta-catenin; p120; catenin; E-CADHERIN; CELL-ADHESION; E-SELECTIN; METASTASIS; BINDING; PROTEINS; CATENIN; CD44; CEA;
D O I
10.1016/j.yexcr.2014.04.007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Oncomarkers play important roles in the detection and management of human malignancies. Carcinoembryonic antigen (CEA, CEACAM5) and epithelial cadherin (E-cadherin) are considered as independent tumor markers in monitoring metastatic colorectal cancer. They are both expressed by cancer cells and can be detected in the blood serum. We investigated the effect of CEA production by MIP101 colorectal carcinoma cell lines on E-cadherin adherens junction (AJ) protein complexes. No direct interaction between E-cadherin and CEA was detected; however, the functional relationships between E-cadherin and its AJ partners: alpha-, beta- and p120 catenins were impaired. We discovered a novel interaction between CEA and beta-catenin protein in the CEA producing cells. It is shown in the current study that CEA overexpression alters the splicing of p120 catenin and triggers the release of soluble E-cadherin. The influence of CEA production by colorectal cancer cells on the function of E-cadherin junction complexes may explain the link between the elevated levels of CEA and the increase in soluble E-cadherin during the progression of colorectal cancer. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:115 / 123
页数:9
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