The cleavage of semaphorin 3C induced by ADAMTS1 promotes cell migration

Cary Esselens, Jordi Malapeira, Núria Colomé, Carmen Casal, Juan Carlos Rodríguez-Manzaneque, Francesc Canals, Joaquín Arribas

    Research output: Contribution to journalArticleResearchpeer-review

    76 Citations (Scopus)

    Abstract

    Metastasis is a sequential process that allows cells to move from the primary tumor and grow elsewhere. Because of their ability to cleave a variety of extracellular signaling and adhesion molecules, metalloproteases have been long considered key components of the metastatic program. However, the function of certain metalloproteases, such as ADAMTS1, is not clear and seems to depend on the cellular environment and/or the stage of tumor progression. To characterize the function of ADAMTS1, we performed two alternative proteomic approaches, difference gel electrophoresis and stable isotope labeling by amino acids in cell culture, to identify novel substrates of the metalloprotease. Both techniques showed that overexpression of ADAMTS1 leads to the release of semaphorin 3C from the extracellular matrix. Although semaphorins are well known regulators of axon guidance, accumulating evidence shows that they may also participate in tumor progression. Here, we show that the cleavage of semaphorin 3C induced by ADAMTS1 promotes the migration of breast cancer cells, indicating that the co-expression of these molecules in tumors may contribute to the metastatic program. © 2010 by The American Society for Biochemistry and Molecular Biology, Inc.
    Original languageEnglish
    Pages (from-to)2463-2473
    JournalJournal of Biological Chemistry
    Volume285
    Issue number4
    DOIs
    Publication statusPublished - 22 Jan 2010

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