Tailoring Fibroblast-Activation Protein Targeting for Theranostics: A Comparative Preclinical Evaluation of the 68Ga- and 177Lu-Labeled Monomeric and Dimeric Fibroblast-Activation Protein Inhibitors DOTA.SA.FAPi and DOTAGA.(SA.FAPi)2

被引:2
|
作者
Lappchen, Tilman [1 ]
Bilinska, Adrianna [1 ]
Pilatis, Eirinaios [1 ]
Menendez, Elena [1 ]
Imlimthan, Surachet [1 ]
Moon, Euy Sung [2 ]
Afshar-Oromieh, Ali [1 ]
Rosch, Frank [2 ]
Rominger, Axel [1 ]
Gourni, Eleni [1 ]
机构
[1] Bern Univ Hosp, Dept Nucl Med, Inselspital, CH-3010 Bern, Switzerland
[2] Johannes Gutenberg Univ Mainz, Dept Chem TRIGA Site, D-55128 Mainz, Germany
来源
MOLECULES | 2024年 / 29卷 / 13期
关键词
fibroblast activation protein inhibitors (FAPi); FAPi-monomer; FAPi-dimer; gallium-68; lutetium-177; RADIONUCLIDE THERAPY; EXPERIENCE; PATIENT; BREAST;
D O I
10.3390/molecules29133093
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: FAP radiopharmaceuticals show promise for cancer diagnosis; however, their limited tumor residency hinders treatment. This study compared two FAPi derivatives, DOTA.SA.FAPi and DOTAGA.(SA.FAPi)(2), labeled with gallium-68 and lutetium-177, aiming to determine an optimum combination for creating theranostic pairs. Methods: The radiotracers were studied for lipophilicity, binding to human serum proteins, and binding to human cancer-associated fibroblasts (CAFs) in vitro, including saturation and internalization/externalization studies. PET/SPECT/CT and biodistribution studies were conducted in PC3 and U87MG xenografts for [Ga-68]Ga-DOTA.SA.FAPi and [Ga-68]Ga-DOTAGA.(SA.FAPi)(2). [Lu-177]Lu-DOTA.SA.FAPi and [Lu-177]Lu-DOTAGA.(SA.FAPi)(2), were evaluated in PC3 xenografts. Biodistribution studies of [Ga-68]Ga-DOTA.SA.FAPi were performed in healthy male and female mice. Results: All radiotracers exhibited strong binding to FAP. Their internalization rate was fast while only [Lu-177]Lu-DOTAGA.(SA.FAPi)(2) was retained longer in CAFs. [Ga-68]Ga-DOTAGA.(SA.FAPi)(2) and [Lu-177]Lu-DOTAGA.(SA.FAPi)(2) displayed elevated lipophilicity and affinity for human serum proteins compared to [Ga-68]Ga-DOTA.SA.FAPi and [Lu-177]Lu-DOTA.SA.FAPi. In vivo studies revealed slower washout of [Ga-68]Ga-DOTAGA.(SA.FAPi)(2) within 3 h compared to [Ga-68]Ga-DOTA.SA.FAPi. The tumor-to-tissue ratios of [Ga-68]Ga-DOTAGA.(SA.FAPi)(2) versus [Ga-68]Ga-DOTA.SA.FAPi did not exhibit any significant differences. [Lu-177]Lu-DOTAGA.(SA.FAPi)(2) maintained a significant tumor uptake even after 96 h p.i. compared to [Lu-177]Lu-DOTA.SA.FAPi. Conclusions: Dimeric compounds hold promise for therapy, while monomers are better suited for diagnostics. Finding the right combination is essential for effective disease management.
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页数:17
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