Mena invasive (MenaINV) promotes multicellular streaming motility and transendothelial migration in a mouse model of breast cancer

Author:

Roussos Evanthia T.1,Balsamo Michele2,Alford Shannon K.2,Wyckoff Jeffrey B.13,Gligorijevic Bojana1,Wang Yarong1,Pozzuto Maria4,Stobezki Robert5,Goswami Sumanta15,Segall Jeffrey E.1,Lauffenburger Douglas A.2,Bresnick Anne R.4,Gertler Frank B.2,Condeelis John S.13

Affiliation:

1. Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, NY 10461, USA

2. David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA 02139, USA

3. Gruss Lipper Biophotonics Center, Albert Einstein College of Medicine, Bronx, NY 10461, USA

4. Department of Biochemistry, Albert Einstein College of Medicine, Bronx, NY 10461, USA

5. Department of Biology, Yeshiva University, New York, NY 10033, USA

Abstract

We have shown previously that distinct Mena isoforms are expressed in invasive and migratory tumor cells in vivo and that the invasion isoform (MenaINV) potentiates carcinoma cell metastasis in murine models of breast cancer. However, the specific step of metastatic progression affected by this isoform and the effects on metastasis of the Mena11a isoform, expressed in primary tumor cells, are largely unknown. Here, we provide evidence that elevated MenaINV increases coordinated streaming motility, and enhances transendothelial migration and intravasation of tumor cells. We demonstrate that promotion of these early stages of metastasis by MenaINV is dependent on a macrophage–tumor cell paracrine loop. Our studies also show that increased Mena11a expression correlates with decreased expression of colony-stimulating factor 1 and a dramatically decreased ability to participate in paracrine-mediated invasion and intravasation. Our results illustrate the importance of paracrine-mediated cell streaming and intravasation on tumor cell dissemination, and demonstrate that the relative abundance of MenaINV and Mena11a helps to regulate these key stages of metastatic progression in breast cancer cells.

Publisher

The Company of Biologists

Subject

Cell Biology

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