组织因子
体内
癌症
癌症研究
抗体
病理
医学
血管内皮生长因子
紫杉醇
胰腺癌
因素七
癌细胞
血管生成
间质细胞
免疫学
生物
内科学
血管内皮生长因子受体
凝结
生物技术
作者
Shijun Zhu,Walter Kisiel,Yang Lu,Lars C. Petersen,John M. Ndungu,Terry W. Moore,Ernest T. Parker,Aiming Sun,Jann N. Sarkaria,James P. Snyder,Dennis C. Liotta,Daniel J. Brat,Bassel F. El‐Rayes,Mamoru Shoji
标识
DOI:10.3109/1061186x.2014.988217
摘要
We have developed a specific technique for imaging cancer in vivo using Cy5.5-labeled factor VIIa (fVIIa), clotting-deficient FFRck-fVIIa, paclitaxel-FFRck-fVIIa, and anti-tissue factor (TF) antibody. FVIIa is the natural ligand for TF. We took advantage of the fact that vascular endothelial cells (VECs) in cancer, but not normal tissue, aberrantly express TF due to its induction by vascular endothelial growth factor (VEGF). Under physiological conditions, TF is expressed by stromal cells and outer blood vessel layers (smooth muscle and adventitia), but not by VECs. We hypothesized that labeled fVIIa or anti-TF antibodies could be used to image the tumor vasculature in vivo. To test this, Cy5.5-labeled fVIIa, FFRck-fVIIa, paclitaxel-FFRck-fVIIa, and anti-TF antibody were developed and administered to athymic nude mice carrying xenografts including glioma U87EGFRviii, pancreatic cancer ASPC-1 and Mia PaCa-2, and squamous cell carcinoma KB-V1. Cy5.5 labeled with these targeting proteins specifically localized to the tumor xenografts for at least 14 days but unconjugated Cy5.5 did not localize to any xenografts or organs. This method of imaging TF in the tumor VECs may be useful in detecting primary tumors and metastases as well as monitoring in vivo therapeutic responses.
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