CXCR4/SDF-1α-mediated chemotaxis in an in vivo model of metastatic esophageal carcinoma.

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Autor/in:
Erscheinungsjahr:
2012
Medientyp:
Text
Schlagworte:
  • Animals
  • Mice
  • Neoplasm Metastasis
  • Chemokine CXCL12/*physiology
  • Chemotaxis/*physiology
  • Esophageal Neoplasms/*pathology
  • Receptors, CXCR4/*physiology
  • Animals
  • Mice
  • Neoplasm Metastasis
  • Chemokine CXCL12/*physiology
  • Chemotaxis/*physiology
  • Esophageal Neoplasms/*pathology
  • Receptors, CXCR4/*physiology
Beschreibung:
  • The chemokine receptor CXCR4 and its ligand (stromal cell-derived factor-1alpha; SDF-1?) play an important role in tumor cell chemotaxis and metastatic homing of esophageal carcinoma. Several methods are available to examine tumor cell migration in vitro. However, in vivo chemotaxis is subject to complex tumor-host interactions. The aim of this study was to establish an in vivo model of chemotaxis for esophageal carcinoma that allows the examination of tumor cell migration and metastatic homing in the complex microenvironment.
  • The chemokine receptor CXCR4 and its ligand (stromal cell-derived factor-1alpha; SDF-1?) play an important role in tumor cell chemotaxis and metastatic homing of esophageal carcinoma. Several methods are available to examine tumor cell migration in vitro. However, in vivo chemotaxis is subject to complex tumor-host interactions. The aim of this study was to establish an in vivo model of chemotaxis for esophageal carcinoma that allows the examination of tumor cell migration and metastatic homing in the complex microenvironment.
Lizenz:
  • info:eu-repo/semantics/restrictedAccess
Quellsystem:
Forschungsinformationssystem des UKE

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Quelldatensatz
oai:pure.atira.dk:publications/f03a3fee-80d4-48ab-862b-84e5f7b7c270