Claudin-2 Promotes Breast Cancer Liver Metastasis by Facilitating Tumor Cell Interactions with Hepatocytes

Author:

Tabariès Sébastien12,Dupuy Fanny13,Dong Zhifeng12,Monast Anie12,Annis Matthew G.12,Spicer Jonathan4,Ferri Lorenzo E.4,Omeroglu Atilla5,Basik Mark6,Amir Eitan7,Clemons Mark8,Siegel Peter M.123

Affiliation:

1. Goodman Cancer Research Centre, McGill University, Montréal, Québec, Canada

2. Departments of Medicine, McGill University, Montréal, Québec, Canada

3. Biochemistry, McGill University, Montréal, Québec, Canada

4. Departments of Surgery, McGill University Health Center, Montréal, Québec, Canada

5. Pathology, McGill University Health Center, Montréal, Québec, Canada

6. Segal Cancer Centre, Sir Mortimer B. Davis Jewish General Hospital, Montréal, Québec, Canada

7. Division of Medical Oncology, University of Toronto and Princess Margaret Hospital, Toronto, Ontario, Canada

8. Division of Medical Oncology, The Ottawa Hospital Cancer Centre, Ottawa, Ontario, Canada

Abstract

ABSTRACT 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 metastases in 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.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

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