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The Synthesis and Initial Evaluation of MerTK Targeted PET Agents

MerTK (Mer tyrosine kinase), a receptor tyrosine kinase, is ectopically or aberrantly expressed in numerous human hematologic and solid malignancies. Although a variety of MerTK targeting therapies are being developed to enhance outcomes for patients with various cancers, the sensitivity of tumors t...

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Detalles Bibliográficos
Autores principales: Wang, Li, Zhou, Yubai, Wu, Xuedan, Ma, Xinrui, Li, Bing, Ding, Ransheng, Stashko, Michael A., Wu, Zhanhong, Wang, Xiaodong, Li, Zibo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8911752/
https://www.ncbi.nlm.nih.gov/pubmed/35268561
http://dx.doi.org/10.3390/molecules27051460
Descripción
Sumario:MerTK (Mer tyrosine kinase), a receptor tyrosine kinase, is ectopically or aberrantly expressed in numerous human hematologic and solid malignancies. Although a variety of MerTK targeting therapies are being developed to enhance outcomes for patients with various cancers, the sensitivity of tumors to MerTK suppression may not be uniform due to the heterogeneity of solid tumors and different tumor stages. In this report, we develop a series of radiolabeled agents as potential MerTK PET (positron emission tomography) agents. In our initial in vivo evaluation, [(18)F]-MerTK-6 showed prominent uptake rate (4.79 ± 0.24%ID/g) in B16F10 tumor-bearing mice. The tumor to muscle ratio reached 1.86 and 3.09 at 0.5 and 2 h post-injection, respectively. In summary, [(18)F]-MerTK-6 is a promising PET agent for MerTK imaging and is worth further evaluation in future studies.