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Radioimmunoimaging of (125)I-labeled anti-CD93 monoclonal antibodies in a xenograft model of non-small cell lung cancer

Lung cancer, especially non-small cell lung cancer (NSCLC), is the most common malignant tumor associated with poor prognosis. Angiogenesis plays a vital role in NSCLC, and could be used in tumor staging and therapy evaluation. CD93 (C1q receptor) is reportedly a key regulator of tumor angiogenesis....

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Detalles Bibliográficos
Autores principales: Liu, Weiwei, Zhang, Chao, Cao, Hui, Shi, Dai, Zhao, Shanshan, Liang, Ting, Hou, Guihua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6896371/
https://www.ncbi.nlm.nih.gov/pubmed/31819775
http://dx.doi.org/10.3892/ol.2019.11036
Descripción
Sumario:Lung cancer, especially non-small cell lung cancer (NSCLC), is the most common malignant tumor associated with poor prognosis. Angiogenesis plays a vital role in NSCLC, and could be used in tumor staging and therapy evaluation. CD93 (C1q receptor) is reportedly a key regulator of tumor angiogenesis. In the present study, the efficacy and specificity of a (125)I-labeled CD93-specific monoclonal antibody ((125)I-anti-CD93 mAb) in detecting NSCLC xenografts were analyzed, and the association between CD93 expression and (125)I-anti-CD93 mAb uptake by tumors was evaluated. The targeting ability of (125)I-anti-CD93 mAb enabled its rapid, continuous and highly specific accumulation in CD93-expressing tumors in vivo. These results revealed the potential applicability of (125)I-anti-CD93 mAb for non-invasive imaging diagnosis of CD93-positive NSCLC.