Claudin-2 Promotes Breast Cancer Liver Metastasis by Facilitating Tumor Cell Interactions with Hepatocytes
Author(s) -
Sébastien Tabariès,
Fanny Dupuy,
Zhifeng Dong,
Anie Monast,
Matthew G. Annis,
Jonathan Spicer,
Lorenzo Ferri,
Atilla Ömeroğlu,
Mark Basik,
Eitan Amir,
Mark Clemons,
Peter M. Siegel
Publication year - 2012
Publication title -
molecular and cellular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.14
H-Index - 327
eISSN - 1067-8824
pISSN - 0270-7306
DOI - 10.1128/mcb.00299-12
Subject(s) - claudin , metastasis , breast cancer , biology , cancer research , liver cancer , cancer , epithelial cell adhesion molecule , cancer cell , hepatocyte , tight junction , cell adhesion molecule , pathology , immunology , medicine , microbiology and biotechnology , in vitro , hepatocellular carcinoma , biochemistry , genetics
We previously identified claudin-2 as a functional mediator of breast cancer liver metastasis. We now confirm that claudin-2 levels are elevated in liver metastases, but not in skin metastases, compared to levels in their matched primary tumors in patients with breast cancer. Moreover, claudin-2 is specifically expressed in liver-metastatic breast cancer cells compared to populations derived from bone or lung metastases. The increased liver tropism exhibited by claudin-2-expressing breast cancer cells requires claudin-2-mediated interactions between breast cancer cells and primary hepatocytes. Furthermore, the reduction of the claudin-2 expression level, either in cancer cells or in primary hepatocytes, diminishes these heterotypic cell-cell interactions. Finally, we demonstrate that the first claudin-2 extracellular loop is essential for mediating tumor cell-hepatocyte interactions and the ability of breast cancer cells to form liver metastasesin vivo . Thus, during breast cancer liver metastasis, claudin-2 shifts from acting within tight-junctional complexes to functioning as an adhesion molecule between breast cancer cells and hepatocytes.
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