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Imaging the distribution of an antibody-drug conjugate constituent targeting mesothelin with (89)Zr and IRDye 800CW in mice bearing human pancreatic tumor xenografts

Mesothelin is a tumor differentiation antigen expressed by epithelial tumors, including pancreatic cancer. Currently, mesothelin is being targeted with an antibody-drug conjugate (ADC) consisting of a mesothelin-specific antibody coupled to a highly potent chemotherapeutic drug. Considering the toxi...

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Detalles Bibliográficos
Autores principales: ter Weele, Eva J., van Scheltinga, Anton G.T. Terwisscha, Kosterink, Jos G.W., Pot, Linda, Vedelaar, Silke R., Lamberts, Laetitia E., Williams, Simon P., Hooge, Marjolijn N. Lub-de, de Vries, Elisabeth G.E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4747211/
https://www.ncbi.nlm.nih.gov/pubmed/26536664
Descripción
Sumario:Mesothelin is a tumor differentiation antigen expressed by epithelial tumors, including pancreatic cancer. Currently, mesothelin is being targeted with an antibody-drug conjugate (ADC) consisting of a mesothelin-specific antibody coupled to a highly potent chemotherapeutic drug. Considering the toxicity of the ADC and reduced accessibility of pancreatic tumors, non-invasive imaging could provide necessary information. We therefore developed a zirconium-89 ((89)Zr) labeled anti-mesothelin antibody ((89)Zr-AMA) to study its biodistribution in human pancreatic tumor bearing mice. Biodistribution and dose-finding of (89)Zr-AMA were studied 144 h after tracer injection in mice with subcutaneously xenografted HPAC. MicroPET imaging was performed 24, 72 and 144 h after tracer injection in mice bearing HPAC or Capan-2. Tumor uptake and organ distribution of (89)Zr-AMA were compared with nonspecific (111)In-IgG. Biodistribution analyses revealed a dose-dependent (89)Zr-AMA tumor uptake. Tumor uptake of (89)Zr-AMA was higher than (111)In-IgG using the lowest tracer dose. MicroPET showed increased tumor uptake over 6 days, whereas activity in blood pool and other tissues decreased. Immunohistochemistry showed that mesothelin was expressed by the HPAC and CAPAN-2 tumors and fluorescence microscopy revealed that AMA-800CW was present in tumor cell cytoplasm. (89)Zr-AMA tumor uptake is antigen-specific in mesothelin-expressing tumors. (89)Zr-AMA PET provides non-invasive, real-time information about AMA distribution and tumor targeting.