Lyn modulates Claudin-2 expression and is a therapeutic target for breast cancer liver metastasis |
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Authors: | Sébastien Tabariès Matthew G. Annis Brian E. Hsu Christine E. Tam Paul Savage Morag Park Peter M. Siegel |
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Affiliation: | 1. Goodman Cancer Research Centre, McGill University, Montréal, Québec, Canada, H3A 1A3;2. Department of Medicine, McGill University, Montréal, Québec, Canada, H3A 1A3;3. Department of Biochemistry, McGill University, Montréal, Québec, Canada, H3A 1A3;4. Department of Oncology, McGill University, Montréal, Québec, Canada, H3A 1A3 |
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Abstract: | Claudin-2 enhances breast cancer liver metastasis and promotes the development of colorectal cancers. The objective of our current study is to define the regulatory mechanisms controlling Claudin-2 expression in breast cancer cells.We evaluated the effect of several Src Family Kinase (SFK) inhibitors or knockdown of individual SFK members on Claudin-2 expression in breast cancer cells. We also assessed the potential effects of pan-SFK and SFK-selective inhibitors on the formation of breast cancer liver metastases. This study reveals that pan inhibition of SFK signaling pathways significantly elevated Claudin-2 expression levels in breast cancer cells. In addition, our data demonstrate that pan-SFK inhibitors can enhance breast cancer metastasis to the liver. Knockdown of individual SFK members reveals that loss of Yes or Fyn induces Claudin-2 expression; whereas, diminished Lyn levels impairs Claudin-2 expression in breast cancer cells. The Lyn-selective kinase inhibitor, Bafetinib (INNO-406), acts to reduce Claudin-2 expression and suppress breast cancer liver metastasis.Our findings may have major clinical implications and advise against the treatment of breast cancer patients with broad-acting SFK inhibitors and support the use of Lyn-specific inhibitors. |
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Keywords: | breast cancer liver metastasis claudins Src family kinase Lyn |
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