Mena invasive (Mena[superscript INV]) and Mena11a isoforms play distinct roles in breast cancer cell cohesion and association with TMEM
نویسندگان
چکیده
Mena, an actin regulatory protein, functions at the convergence of motility pathways that drive breast cancer cell invasion and migration in vivo. The tumor microenvironment spontaneously induces both increased expression of the MenaINV and decreased expression of Mena11a isoforms in invasive and migratory tumor cells. Tumor cells with this Mena expression pattern participate with macrophages in migration and intravasation in mouse mammary tumors in vivo. Consistent with these findings, anatomical sites containing tumor cells with high levels of Mena expression associated with perivascular macrophages were identified in human invasive ductal breast carcinomas and called TMEM. The number of TMEM sites positively correlated with the development of distant metastasis in humans. Here we demonstrate that mouse mammary tumors generated from EGFP-MenaINV expressing tumor cells are significantly less cohesive and have discontinuous cell-cell contacts compared to Mena11a xenografts. Using the mouse PyMT model we show that metastatic mammary tumors express 8.7 fold more total Mena and 7.5 fold more MenaINV mRNA than early non-metastatic ones. Furthermore, MenaINV expression in fine needle aspiration biopsy (FNA) samples of human invasive ductal carcinomas correlate with TMEM score while Mena11a does not. These results suggest that MenaINV is the isoform associated with breast cancer cell discohesion, invasion and intravasation in mice and in humans. They also imply that MenaINV expression and TMEM score measure related aspects of a common tumor cell dissemination mechanism and provide new insight into metastatic risk. Correspondence: Evanthia T. Roussos [email protected], (718) 678-1131, John Condeelis [email protected], Maja H. Oktay, (718) 920-6091,[email protected]. Evanthia T. Roussos ([email protected]), Sumanta Goswami ([email protected]), Michele Balsamo ([email protected]), Yarong Wang ([email protected]), Robert Stobezki ([email protected]), Esther Adler ([email protected]), Brian D. Robinson ([email protected]), Joan G. Jones ([email protected]), Frank B. Gertler ([email protected]), John S. Condeelis ([email protected]), Maja H. Oktay ([email protected]) NIH Public Access Author Manuscript Clin Exp Metastasis. Author manuscript; available in PMC 2012 September 27. Published in final edited form as: Clin Exp Metastasis. 2011 August ; 28(6): 515–527. doi:10.1007/s10585-011-9388-6. N IH PA Athor M anscript N IH PA Athor M anscript N IH PA Athor M anscript
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Mena invasive (MenaINV) promotes multicellular streaming motility and transendothelial migration in a mouse model of breast cancer.
We have shown previously that distinct Mena isoforms are expressed in invasive and migratory tumor cells in vivo and that the invasion isoform (Mena(INV)) 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...
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