Identification of invasion specific splice variants of the cytoskeletal protein Mena present in mammary tumor cells during invasion in vivo.

TitleIdentification of invasion specific splice variants of the cytoskeletal protein Mena present in mammary tumor cells during invasion in vivo.
Publication TypeJournal Article
Year of Publication2009
AuthorsGoswami, S, Philippar, U, Sun, D, Patsialou, A, Avraham, J, Wang, W, Di Modugno, F, Nistico, P, Gertler, FB, Condeelis, JS
JournalClin Exp Metastasis
Volume26
Issue2
Pagination153-9
Date Published2009
ISSN1573-7276
KeywordsAdenocarcinoma, Animals, Breast Neoplasms, Chemotaxis, Humans, Mammary Neoplasms, Experimental, Mice, Mice, SCID, Microfilament Proteins, Neoplasm Invasiveness, Neoplasm Metastasis, Neoplasm Transplantation, Protein Isoforms, Rats, Transplantation, Heterologous
Abstract

We have studied the gene expression pattern of invasive primary mammary tumor cells using a unique in vivo invasion assay that isolates the invasive tumor cells by chemotaxis. One of the genes upregulated in the invasive tumor cells is Mena, an actin binding protein involved in the regulation of cell motility. There are multiple known splice variants of Mena accounted for by four alternatively included exons, +, ++, +++ and 11a. Using the in vivo invasion assay in rats and mice with mammary tumors we observed that two isoforms of Mena, ++ and +++, are upregulated in the invasive tumor cells and one isoform, 11a, is downregulated. The Mena isoform switching pattern described here may provide a new biomarker for the presence of metastatic cancer cells and for prognosis.

DOI10.1007/s10585-008-9225-8
Alternate JournalClin. Exp. Metastasis
PubMed ID18985426
PubMed Central IDPMC3042857
Grant List1-U54-CA112967 / CA / NCI NIH HHS / United States
CA 100324 / CA / NCI NIH HHS / United States
CA113395 / CA / NCI NIH HHS / United States
GM58801 / GM / NIGMS NIH HHS / United States
P01 CA100324-06 / CA / NCI NIH HHS / United States
R01 CA113395-04 / CA / NCI NIH HHS / United States
R01 GM058801-10 / GM / NIGMS NIH HHS / United States

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