86/90Y-Labeled Monoclonal Antibody Targeting Tissue Factor for Pancreatic Cancer Theranostics

被引:19
|
作者
Ferreira, Carolina A. [4 ]
Ehlerding, Emily B. [1 ]
Rosenkrans, Zachary T. [3 ]
Jiang, Dawei [1 ]
Sun, Tuanwei [1 ]
Aluicio-Sarduy, Eduardo [1 ]
Engle, Jonathan W. [1 ]
Ni, Dalong [1 ]
Cai, Weibo [2 ,3 ]
机构
[1] Univ Wisconsin, Dept Radiol & Med Phys, Madison, WI 53705 USA
[2] Univ Wisconsin, Dept Radiol & Med Phys, Dept Biomed Engn, Madison, WI 53705 USA
[3] Univ Wisconsin, Dept Pharmaceut Sci, Madison, WI 53705 USA
[4] Univ Wisconsin, Dept Biomed Engn, Madison, WI 53705 USA
基金
美国国家卫生研究院;
关键词
tissue factor; positron emission tomography (PET); radioimmunotherapy; yttrium-86; yttrium-90; theranostics; pancreatic cancer; FACTOR EXPRESSION; PHASE-I; THERAPY; PET; ANGIOGENESIS; INHIBITION; THROMBOSIS;
D O I
10.1021/acs.molpharmaceut.0c00127
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Pancreatic cancer is highly aggressive, with a median survival time of less than 6 months and a 5-year overall survival rate of around 7%. The poor prognosis of PaCa is largely due to its advanced stage at diagnosis and the lack of efficient therapeutic options. Thus, the development of an efficient, multifunctional PaCa theranostic system is urgently needed. Overexpression of tissue factor (TF) has been associated with increased tumor growth, angiogenesis, and metastasis in many malignancies, including pancreatic cancer. Herein, we propose the use of a TFtargeted monoclonal antibody (ALT836) conjugated with the pair Y-86(/)90 as a theranostic agent against pancreatic cancer. For methods, serial PET imaging with (86)YDTPA-ALT836 was conducted to map the biodistribution the tracer in BXPC-3 tumor-bearing mice. Y-90-DTPA-ALT836 was employed as a therapeutic agent that also allowed tumor burden monitoring through Cherenkov luminescence imaging. The results were that the uptake of Y-86-DTPA-ALT836 in BXPC-3 xenograft tumors was high and increased over time up to 48 h postinjection (p.i.), corroborated through ex vivo biodistribution studies and further confirmed by Cherenkov luminescence Imaging. In therapeutic studies, Y-90-DTPA-ALT836 was found to slow tumor growth relative to the control groups and had significantly smaller (p < 0.05) tumor volumes 1 day p.i. Histological analysis of ex vivo tissues revealed significant damage to the treated tumors. The conclusion is that the use of the Y-86(/90) theranostic pair allows PET imaging with excellent tumor-to-background contrast and treatment of TF-expressing pancreatic tumors with promising therapeutic outcomes.
引用
收藏
页码:1697 / 1705
页数:9
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