EDB Fibronectin Specific Peptide for Prostate Cancer Targeting

被引:81
作者
Han, Zheng [1 ]
Zhou, Zhuxian [1 ]
Shi, Xiaoyue [1 ]
Wang, Junpeng [1 ]
Wu, Xiaohui [1 ]
Sun, Da [1 ]
Chen, Yinghua [2 ]
Zhu, Hui [3 ]
Magi-Galluzzi, Cristina [4 ]
Lu, Zheng-Rong [1 ]
机构
[1] Case Western Reserve Univ, Dept Biomed Engn, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Dept Physiol & Biophys, Cleveland, OH 44106 USA
[3] Cleveland Clin Fdn, Glickman Urol Inst, Cleveland, OH 44106 USA
[4] Cleveland Clin Fdn, Robert J Tomsich Pathol & Lab Med Inst, Cleveland, OH 44106 USA
关键词
EPITHELIAL-MESENCHYMAL TRANSITION; ONCOFETAL FIBRONECTIN; REACTIVE STROMA; IN-VITRO; PROGRESSION; THERAPY; LOCALIZATION; EXPRESSION; MARKER; GRADE;
D O I
10.1021/acs.bioconjchem.5b00178
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Extradomain-B fibronectin (EDB-FN), one of the oncofetal fibronectin (onfFN) isoforms, is a high-molecular-weight glycoprbtein that mediates cell adhesion and migration. The expression of EDB-FN is associated with a number of cancer-related biological processes such as tumorigenesis, angiogenesis, and epithelial-to-mesenchymal transition (EMT). Here, we report the development of a small peptide specific to EDB-FN for targeting prostate cancer. A cyclic nonapeptide, CTVRTSADC (ZD2), was identified using peptide phage display. A ZD2-Cy5 conjugate was synthesized to accomplish molecular imaging of prostate cancer in vitro and in vivo. ZD2-Cy5 demonstrated effective binding to up-regulated EDB-FN secreted by TGF-beta-induced PC3 cancer cells following EMT. Following intravenous injections, the targeted fluorescent probe specifically bound to and delineated PC3-GFP prostate tumors in nude mice bearing the tumor xenografts. ZD2-Cy5 also showed stronger binding to human prostate tumor specimens with a higher Gleason score (GS9) compared to those with a lower score (GS 7), with no binding in benign prostatic hyperplasia (BPH). Thus, the ZD2 peptide is a promising strategy for molecular imaging and targeted therapy of prostate cancer.
引用
收藏
页码:830 / 838
页数:9
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