Details

Autor(en) / Beteiligte

• Liu, Kehuang
• Jiang, Tao
• Rao, Wanqian
• Chen, Bei
• Yin, Xiaoqin
• Xu, Pengfei
• Hu, Shuo

Titel

Peptidic heterodimer-based radiotracer targeting fibroblast activation protein and integrin αvβ3

Ist Teil von

• European journal of nuclear medicine and molecular imaging, 2024-05, Vol.51 (6), p.1544-1557

Ort / Verlag

Berlin/Heidelberg: Springer Berlin Heidelberg

Erscheinungsjahr

2024

Quelle

Alma/SFX Local Collection

Beschreibungen/Notizen

• Purpose Several studies have demonstrated the advantages of heterodimers over their corresponding monomers due to the multivalency effect. This effect leads to an increased number of effective targeted receptors and, consequently, improved tumor uptake. Fibroblast activation protein (FAP) and integrin α v β 3 are found to be overexpressed in different components of the tumor microenvironment. In our pursuit of enhancing tumor uptake and retention, we designed and developed a novel peptidic heterodimer that synergistically targets both FAP and integrin α v β 3 . Methods FAP-RGD was synthesized from FAP-2286 and c(RGDfK) through a multi-step organic synthesis. The dual receptor binding property of 68 Ga-FAP-RGD was investigated by cell uptake and competitive binding assays. Preclinical pharmacokinetics were determined in HT1080-FAP and U87MG tumor models using micro-positron emission tomography/computed tomography (micro-PET/CT) and biodistribution studies. The antitumor efficacy of 177 Lu-FAP-RGD was assessed in U87MG tumor models. The radiation exposure and clinical diagnostic performance of 68  Ga-FAP-RGD were evaluated in healthy volunteers and cancer patients. Results Bi-specific radiotracer 68 Ga-FAP-RGD exhibited high binding affinity for both FAP and integrin α v β 3 . In comparison to 68 Ga-FAP-2286 and 68 Ga-RGDfK, 68 Ga-FAP-RGD displayed enhanced tumor uptake and longer tumor retention time in preclinical models. 177 Lu-FAP-RGD could efficiently suppress the growth of U87MG tumor in vivo when applied at an activity of 18.5 and 29.6 MBq. The effective dose of 68 Ga-FAP-RGD was 1.06 × 10 −2  mSv/MBq. 68 Ga-FAP-RGD demonstrated low background activity and stable accumulation in most neoplastic lesions up to 3 h. Conclusion Taking the advantages of multivalency effect, the bi-specific radiotracer 68 Ga-FAP-RGD showed superior tumor uptake and retention compared to its corresponding monomers. Preclinical studies with 68 Ga- or 177 Lu-labeled FAP-RGD showed favorable image contrast and effective antitumor responses. Despite the excellent performance of 68 Ga-FAP-RGD in clinical diagnosis, experimental efforts are currently underway to optimize the structure of FAP-RGD to increase its potential for clinical application in endoradiotherapy.