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Preclinical evaluation of (111)In-DTPA-INCA-X anti-Ku70/Ku80 monoclonal antibody in prostate cancer.
Evans-Axelsson, Susan; Vilhelmsson Timmermand, Oskar; Welinder, Charlotte; Borrebaeck, Carl Ak; Strand, Sven-Erik; Tran, Thuy A; Jansson, Bo; Bjartell, Anders.
Afiliação
  • Evans-Axelsson S; Division of Urological Cancers, Department of Clinical Sciences Malmö, Lund University Sweden.
  • Vilhelmsson Timmermand O; Department of Medical Radiation Physics, Clinical Sciences, Lund University Lund, Sweden.
  • Welinder C; Department of Oncology, Clinical Sciences, Lund University Lund, Sweden.
  • Borrebaeck CA; Department of Immunotechnology and CREATE Health Translational Cancer Center, Lund University Medicon Village, Lund, Sweden.
  • Strand SE; Department of Medical Radiation Physics, Clinical Sciences, Lund University Lund, Sweden ; Lund University Bioimaging Center Lund, Sweden.
  • Tran TA; Lund University Bioimaging Center Lund, Sweden.
  • Jansson B; Department of Oncology, Clinical Sciences, Lund University Lund, Sweden.
  • Bjartell A; Division of Urological Cancers, Department of Clinical Sciences Malmö, Lund University Sweden.
Am J Nucl Med Mol Imaging ; 4(4): 311-23, 2014.
Article em En | MEDLINE | ID: mdl-24982817
ABSTRACT
The aim of this investigation was to assess the Ku70/Ku80 complex as a potential target for antibody imaging of prostate cancer. We evaluated the in vivo and ex vivo tumor targeting and biodistribution of the (111)In-labeled human internalizing antibody, INCA-X ((111)In-DTPA-INCA-X antibody), in NMRI-nude mice bearing human PC-3, PC-3M-Lu2 or DU145 xenografts. DTPA-conjugated, non-labeled antibody was pre-administered at different time-points followed by a single intravenous injection of (111)In-DTPA-INCA-X. At 48, 72 and 96 h post-injection, tissues were harvested, and the antibody distribution was determined by measuring radioactivity. Preclinical SPECT/CT imaging of mice with and without the predose was performed at 48 hours post-injection of labeled DTPA-INCA-X. Biodistribution of the labeled antibody showed enriched activity in tumor, spleen and liver. Animals pre-administered with DTPA-INCA-X showed increased tumor uptake and blood content of (111)In-DTPA-INCA-X with reduced splenic and liver uptake. The in vitro and in vivo data presented show that the (111)In-labeled INCA-X antibody is internalized into prostate cancer cells and by pre-administering non-labeled DTPA-INCA-X, we were able to significantly reduce the off target binding and increase the (111)In-DTPA-INCA-X mAb uptake in PC-3, PC-3M-Lu2 and DU145 xenografts. The results are encouraging and identifying the Ku70/Ku80 antigen as a target is worth further investigation for functional imaging of prostate cancer.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2014 Tipo de documento: Article