<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>D'Agostino, Gianluca</dc:creator>
  <dc:creator>Cecchinato, Valentina</dc:creator>
  <dc:creator>Uguccioni, Mariagrazia</dc:creator>
  <dc:date>2018-09-25</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Infiltrating immune cells are a key component of the tumor microenvironment and play central roles in  dictating tumor fate, either promoting anti-tumor immune responses, or sustaining tumor growth,  angiogenesis and metastasis. A distinctive microenvironment is often associated to different tumor  types, with substantial differences in prognosis. The production of a variety of chemotactic factors by  cancer and stromal cells orchestrates cell recruitment, local immune responses or cancer progression.  In the last decades, different studies have highlighted how chemotactic cues, and in particular  chemokines, can act as natural antagonists or induce synergistic effects on selective receptors by  forming heterocomplexes, thus shaping migratory responses of immune cells. A variety of chemokines  has been described to be able to form heterocomplexes both in vitro and in vivo under inflammatory  conditions, but nowadays little is known on the presence and relevance of heterocomplexes in the  tumor microenvironment. In recent years, the alarmin HMGB1, which can be massively released within  the tumor microenvironment, has also been described to form a complex with the chemokine CXCL12  enhancing CXCR4-mediated signaling, thus providing an additional regulation of the activity of the  chemokine system. In the present review, we will discuss the current knowledge on the synergy  occurring between chemokines or inflammatory molecules, and describe the multiple functions exerted  by the chemokines expressed in the tumor microenvironment, pointing our attention to the synergism  as a possible modulator of tumor suppression or progression.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://susi.usi.ch/global/documents/318964</dc:identifier>
  <dc:identifier>https://n2t.net/ark:/12658/srd1318964</dc:identifier>
  <dc:identifier>https://susi.usi.ch/documents/318964/files/DAgostino_FI_2018.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.3389/fimmu.2018.02185</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/ark/12658/srd1318964</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>CC BY</dc:rights>
  <dc:source>Frontiers in immunology. - 2018, vol. 9, p. 2185</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Chemokines</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Tumor microenvironment</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Heterocomplexes</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">CXCL12</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">HMGB1</dc:subject>
  <dc:subject>info:eu-repo/classification/udc/61</dc:subject>
  <dc:title xmlns:ns6="xml" ns6:lang="en">Chemokine heterocomplexes and cancer : a novel chapter to be written in tumor immunity</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
