期刊
BIOCONJUGATE CHEMISTRY
卷 28, 期 9, 页码 2361-2371出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.bioconjchem.7b00374
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资金
- Region Pays de la Loire within the Erasmus-Mundus Program NanoFar
- University of Liege
- FNRS
- European Regional Development Fund
- Walloon Region
- Fondation ULB
- Fonds Erasme
- Association Vincotte Nuclear (AVN)
Epidermal growth-factor receptor (EGFR) is involved in cell growth and proliferation and is over-expressed in malignant tissues. Although anti-EGFR-based inimunotherapy became a standard of care for patients with EGFR-positive tumors, this strategy of addressing cancer tumors by targeting EGFR with monoclonal antibodies is less-developed for patient diagnostic and monitoring. Indeed, antibodies exhibit a slow blood clearance, which is detrimental for positron emission tomography (PET) imaging. New molecular probes are proposed to overcome such limitations for patient monitoring, making use of low-molecular-weight protein scaffolds as alternatives to antibodies, such as Nanofitins with better pharmacokinetic profiles. Anti-EGFR Nanofitin B10 was reformatted by genetic engineering to exhibit a unique cysteine moiety at its C-terminus, which allows the development of a fast and site-specific radiolabeling procedure with F-18-4-fluorobenzamido-N-ethylamino-maleimide (F-18-FBEM). The in vivo tumor targeting and imaging profile of the anti-EGFR Cys B10 Nanofitin was investigated in a double-tumor xenograft model by static small-animal PET at 2 h after tail-vein injection of the radiolabeled Nanofitin F-18 FBEM Cys B10. The image showed that the EGFR-positive tumor (A431) is clearly delineated in comparison to the EGFR-negative tumor (H520) with a significant tumor-to background contrast. F-18 FBEM Cys B10 demonstrated a significantly higher retention in A431 tumors than in H520 tumors at 2.5 h post-injection with a A431-to-H520 uptake ratio of 2.53 +/- 0.18 and a tumor-to-blood ratio of 4.55 +/- 0.63. This study provides the first report of Nanofitin scaffold used as a targeted PET radiotracer for in vivo imaging of EGFR-positive tumor, with the anti-EGFR BIO Nanofitin used as proof-of-concept. The fast generation of specific Nanofitins via a fully in vitro selection process, together with the excellent imaging features of the Nanofitin scaffold, could facilitate the development of valuable PET-based companion diagnostics.
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