Filamin A regulates focal adhesion disassembly and suppresses breast cancer cell migration and invasion

Author:

Xu Yingjie1111,Bismar Tarek A.2,Su Jie1111,Xu Bin1111,Kristiansen Glen3,Varga Zsuzsanna3,Teng Lianghong2,Ingber Donald E.4445,Mammoto Akiko444,Kumar Rakesh6,Alaoui-Jamali Moulay A.1111

Affiliation:

1. Lady Davis Institute for Medical Research and Segal Cancer Centre, Jewish General Hospital, Department of Medicine and Department of Oncology, Faculty of Medicine, McGill University, Montreal, Quebec H3T 1E2, Canada

2. Department of Pathology and Laboratory Medicine, Faculty of Medicine, University of Calgary, Calgary, Alberta T2L 2K8, Canada

3. Institute of Surgical Pathology, University Hospital Zurich, 8091 Zurich, Switzerland

4. Vascular Biology Program, Department of Pathology, and Deparment of Surgery, Children’s Hospital Boston, Harvard Medical School, Boston, MA 02115

5. Wyss Institute for Biologically Inspired Engineering at Harvard University, Boston, MA 02115

6. Department of Biochemistry and Molecular Biology, The George Washington University Medical Center, Washington, DC 20037

Abstract

The actin cross-linking protein filamin A (FLNa) functions as a scaffolding protein and couples cell cytoskeleton to extracellular matrix and integrin receptor signaling. In this study, we report that FLNa suppresses invasion of breast cancer cells and regulates focal adhesion (FA) turnover. Two large progression tissue microarrays from breast cancer patients revealed a significant decrease of FLNa levels in tissues from invasive breast cancer compared with benign disease and in lymph node–positive compared with lymph node–negative breast cancer. In breast cancer cells and orthotopic mouse breast cancer models, down-regulation of FLNa stimulated cancer cell migration, invasion, and metastasis formation. Time-lapse microscopy and biochemical assays after FLNa silencing and rescue with wild-type or mutant protein resistant to calpain cleavage revealed that FLNa regulates FA disassembly at the leading edge of motile cells. Moreover, FLNa down-regulation enhanced calpain activity through the mitogen-activated protein kinase–extracellular signal-regulated kinase cascade and stimulated the cleavage of FA proteins. These results document a regulation of FA dynamics by FLNa in breast cancer cells.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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