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Disclosing the CXCR4 expression in lymphoproliferative diseases by targeted molecular imaging.
Wester, Hans Jürgen; Keller, Ulrich; Schottelius, Margret; Beer, Ambros; Philipp-Abbrederis, Kathrin; Hoffmann, Frauke; Simecek, Jakub; Gerngross, Carlos; Lassmann, Michael; Herrmann, Ken; Pellegata, Natalia; Rudelius, Martina; Kessler, Horst; Schwaiger, Markus.
Afiliación
  • Wester HJ; 1. Pharmaceutical Radiochemistry, Technische Universität München, Garching, Germany.
  • Keller U; 2. III. Medical Department, Technische Universität München, Munich, Germany.
  • Schottelius M; 1. Pharmaceutical Radiochemistry, Technische Universität München, Garching, Germany.
  • Beer A; 3. Department of Nuclear Medicine, Technische Universität München, Munich, Germany.
  • Philipp-Abbrederis K; 2. III. Medical Department, Technische Universität München, Munich, Germany.
  • Hoffmann F; 1. Pharmaceutical Radiochemistry, Technische Universität München, Garching, Germany.
  • Simecek J; 1. Pharmaceutical Radiochemistry, Technische Universität München, Garching, Germany.
  • Gerngross C; 3. Department of Nuclear Medicine, Technische Universität München, Munich, Germany.
  • Lassmann M; 4. Department of Nuclear Medicine, University Hospital Würzburg, Würzburg, Germany.
  • Herrmann K; 4. Department of Nuclear Medicine, University Hospital Würzburg, Würzburg, Germany.
  • Pellegata N; 5. Institute of Pathology, Helmholtz Zentrum München, Munich, Germany.
  • Rudelius M; 6. Institute of Pathology, Universität Würzburg, Comprehensive Cancer Center Mainfranken, Würzburg, Germany.
  • Kessler H; 7. Institute for Advanced Study, Department of Chemistry, Technische Universität München, Garching, Germany ; 8. Chemistry Department, Faculty of Science, King Abdulaziz University, Jeddah, Saudi Arabia.
  • Schwaiger M; 3. Department of Nuclear Medicine, Technische Universität München, Munich, Germany.
Theranostics ; 5(6): 618-30, 2015.
Article en En | MEDLINE | ID: mdl-25825601
ABSTRACT
Chemokine ligand-receptor interactions play a pivotal role in cell attraction and cellular trafficking, both in normal tissue homeostasis and in disease. In cancer, chemokine receptor-4 (CXCR4) expression is an adverse prognostic factor. Early clinical studies suggest that targeting CXCR4 with suitable high-affinity antagonists might be a novel means for therapy. In addition to the preclinical evaluation of [(68)Ga]Pentixafor in mice bearing human lymphoma xenografts as an exemplary CXCR4-expressing tumor entity, we report on the first clinical applications of [(68)Ga]Pentixafor-Positron Emission Tomography as a powerful method for CXCR4 imaging in cancer patients. [(68)Ga]Pentixafor binds with high affinity and selectivity to human CXCR4 and exhibits a favorable dosimetry. [(68)Ga]Pentixafor-PET provides images with excellent specificity and contrast. This non-invasive imaging technology for quantitative assessment of CXCR4 expression allows to further elucidate the role of CXCR4/CXCL12 ligand interaction in the pathogenesis and treatment of cancer, cardiovascular diseases and autoimmune and inflammatory disorders.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Péptidos Cíclicos / Linfoma de Células B Grandes Difuso / Radiofármacos / Receptores CXCR4 / Tomografía de Emisión de Positrones / Complejos de Coordinación Tipo de estudio: Prognostic_studies Límite: Animals / Female / Humans / Male Idioma: En Revista: Theranostics Año: 2015 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Péptidos Cíclicos / Linfoma de Células B Grandes Difuso / Radiofármacos / Receptores CXCR4 / Tomografía de Emisión de Positrones / Complejos de Coordinación Tipo de estudio: Prognostic_studies Límite: Animals / Female / Humans / Male Idioma: En Revista: Theranostics Año: 2015 Tipo del documento: Article País de afiliación: Alemania