1 Ocak 2009 Dergi makalesi Açık Erişim

Larue, L.; Luciani, F.; Kumasaka, M.; Champeval, D.; Demirkan, N.; Bonaventure, J.; Delmas, V.

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  <identifier identifierType="URL">https://aperta.ulakbim.gov.tr/record/40269</identifier>
  <creators>
    <creator>
      <creatorName>Larue, L.</creatorName>
      <givenName>L.</givenName>
      <familyName>Larue</familyName>
    </creator>
    <creator>
      <creatorName>Luciani, F.</creatorName>
      <givenName>F.</givenName>
      <familyName>Luciani</familyName>
    </creator>
    <creator>
      <creatorName>Kumasaka, M.</creatorName>
      <givenName>M.</givenName>
      <familyName>Kumasaka</familyName>
    </creator>
    <creator>
      <creatorName>Champeval, D.</creatorName>
      <givenName>D.</givenName>
      <familyName>Champeval</familyName>
    </creator>
    <creator>
      <creatorName>Demirkan, N.</creatorName>
      <givenName>N.</givenName>
      <familyName>Demirkan</familyName>
    </creator>
    <creator>
      <creatorName>Bonaventure, J.</creatorName>
      <givenName>J.</givenName>
      <familyName>Bonaventure</familyName>
    </creator>
    <creator>
      <creatorName>Delmas, V.</creatorName>
      <givenName>V.</givenName>
      <familyName>Delmas</familyName>
    </creator>
  </creators>
  <titles>
    <title>Bypassing Melanocyte Senescence By Beta-Catenin: A Novel Way To Promote Melanoma</title>
  </titles>
  <publisher>Aperta</publisher>
  <publicationYear>2009</publicationYear>
  <dates>
    <date dateType="Issued">2009-01-01</date>
  </dates>
  <resourceType resourceTypeGeneral="Text">Journal article</resourceType>
  <alternateIdentifiers>
    <alternateIdentifier alternateIdentifierType="url">https://aperta.ulakbim.gov.tr/record/40269</alternateIdentifier>
  </alternateIdentifiers>
  <relatedIdentifiers>
    <relatedIdentifier relatedIdentifierType="DOI" relationType="IsIdenticalTo">10.1016/j.patbio.2008.11.003</relatedIdentifier>
  </relatedIdentifiers>
  <rightsList>
    <rights rightsURI="http://www.opendefinition.org/licenses/cc-by">Creative Commons Attribution</rights>
    <rights rightsURI="info:eu-repo/semantics/openAccess">Open Access</rights>
  </rightsList>
  <descriptions>
    <description descriptionType="Abstract">The Wnt/beta-catenin signaling pathway plays a key role in several cellular functions during embryonic development and adult homeostasis. The deregulation of this pathway may lead to the development of cancer, including melanoma. Deregulation of the Wnt/beta-catenin pathway occurs through either the induction/repression of, or specific mutations in, various members of this signaling pathway; this results in the stabilization of beta-catenin and its translocation from the cytoplasm to the nucleus, where it regulates transcription. Although nuclear beta-catenin is clearly involved in malignant transformation, the mechanism by which it exerts its effects remains elusive. This review focuses on the molecular and cellular mechanisms that are driven by beta-catenin and lead to melanocyte transformation. In particular, we describe how beta-catenin induces melanocyte immortalization, a novel activity of this multifunction protein. Finally, we discuss how beta-catenin-induced immortalization can cooperate with MAPKinase pathways to produce melanoma. (C) 2008 Elsevier Masson SAS. All rights reserved.</description>
  </descriptions>
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