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    <title>Burgers, S.A.</title>
    <link>http://repub.eur.nl/res/aut/6834/</link>
    <description>List of Publications</description>
    <language>en</language>
    <image>
      <url>http://repub.eur.nl/static-eur/img/logo.png</url>
      <title>RePub, Erasmus University Rotterdam</title>
      <link>http://repub.eur.nl</link>
    </image>
    <item>
      <title>Proteomic analysis of exosomes isolated from human malignant pleural effusions. (Article)</title>
      <link>http://repub.eur.nl/res/pub/13308/</link>
      <pubDate>2004-07-01T00:00:00Z</pubDate>
      <description>Exosomes are membrane vesicles from endosomal origin secreted by various
      cells such as hematopoietic, epithelial, and tumor cells. Exosomes
      secreted by tumor cells contain specific antigens potentially useful for
      immunotherapeutic purposes. Our aim was to determine if exosomes are
      present in human cancerous pleural effusions and to identify their
      proteomic content. Exosomes were purified by sucrose gradient
      ultracentrifugation, and electron microscopy was used to check both
      concentration and purity of exosomes. Proteins were separated by
      one-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis,
      and protein bands were identified by matrix-assisted laser desorption
      ionization time-of-flight mass spectrometry and Western blotting. Exosomes
      were present in pleural fluid obtained from patients suffering from
      mesothelioma (n = 4), lung cancer (n = 2), breast cancer (n = 2), and
      ovarian cancer (n = 1). As previously reported by others,
      antigen-presenting molecules, cytoskeletal proteins, and signal
      transduction-involved proteins were present. Proteins not previously
      reported were identified (SNX25, BTG1, PEDF, thrombospondin 2). Different
      types of immunoglobulins and complement factors were abundantly present in
      the sucrose fractions containing exosomes. Exosome-directed specificity of
      these immunoglobulins was not observed. In conclusion, sucrose gradient
      ultracentrifugation allows isolation of exosomes from malignant pleural
      effusions. However, pleural fluid proteins and especially immunoglobulins
      are coisolated and may hamper the use of exosomes isolated from malignant
      effusion for immunotherapy programs.</description>
    </item> <item>
      <title>Proteomic analysis of exosomes secreted by human mesothelioma cells (Article)</title>
      <link>http://repub.eur.nl/res/pub/10335/</link>
      <pubDate>2004-01-01T00:00:00Z</pubDate>
      <description>Exosomes are small membrane vesicles secreted into the extracellular
      compartment by exocytosis. Tumor exosomes may be involved in the sampling
      of antigens to antigen presenting cells or as decoys allowing the tumor to
      escape immune-directed destruction. The proteins present in exosomes
      secreted by tumor cells have been poorly defined. This study describes the
      protein composition of mesothelioma cell-derived exosomes in more detail.
      After electrophoresis of exosome preparations, matrix-assisted laser
      desorption ionization time-of-flight (MALDI-TOF) was used to characterize
      the protein spots. MHC class I was found to be present together with the
      heat shock proteins HSC70 and HSP90. In addition, we found annexins and
      PV-1, proteins involved in membrane transport and function. Cytoskeleton
      proteins and their associated proteins ezrin, moesin, actinin-4,
      desmoplakin, and fascin were also detected. Besides the molecular motor
      kinesin-like protein, many enzymes were detected revealing the cytoplasmic
      orientation of exosomes. Most interesting was the detection of
      developmental endothelial locus-1 (DEL-1), which can act as a strong
      angiogenic factor and can increase the vascular development in the
      neighborhood of the tumor. In conclusion, mesothelioma cells release
      exosomes that express a discrete set of proteins involved in antigen
      presentation, signal transduction, migration, and adhesion. Exosomes may
      play an important role in the interaction between tumor cells and their
      environment.</description>
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