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1.
Eur J Med Chem ; 269: 116278, 2024 Apr 05.
Article in English | MEDLINE | ID: mdl-38479165

ABSTRACT

Asialoglycoprotein receptor (ASGPR) specifically recognizes glycans terminated with ß-d-galactose or N-acetylgalactosamine. Its exclusive expression in mammalian hepatocytes renders it an ideal hepatic-targeted biomarker. To date, ASGPR-targeted ligands have been actively developed for drug delivery and hepatic imaging. This review provides a comprehensive summary of the progress achieved to-date in the field of developing ASGPR-targeted nuclear medicine imaging (NMI) radiotracers, highlighting the recent advancements over the last decade in terms of structure, radionuclides and labeling strategies. The biodistribution patterns, imaging characteristics, challenges and future prospective are discussed.


Subject(s)
Nuclear Medicine , Animals , Asialoglycoprotein Receptor/chemistry , Asialoglycoprotein Receptor/metabolism , Hepatocytes/metabolism , Liver/diagnostic imaging , Liver/metabolism , Mammals/metabolism , Tissue Distribution , Acetylgalactosamine/chemistry , Acetylgalactosamine/metabolism
2.
Nucl Med Commun ; 43(7): 746-755, 2022 Jul 01.
Article in English | MEDLINE | ID: mdl-35506275

ABSTRACT

Fibroblast activation protein (FAP) is a type II transmembrane protein, which is over-expressed in cancer-associated fibroblasts (CAFs). CAFs are tumor stromal cells that constitute a major component of cancer volume and are reportedly related to tumorigenesis, angiogenesis, metastasis, promotion of drug resistance and induction of tumor immunity. FAP is widely acknowledged as the signature protein of CAFs. At present, FAP inhibitors (FAPI) have achieved ideal results in tumor PET/computed tomography (CT) imaging. Theoretically, FAP-targeted drugs can inhibit tumor progression. Nonetheless, no satisfactory therapeutic effect has been observed so far, which has impeded their implementation in clinical practice. In this review, we describe the characteristics of FAP and its role in the occurrence and development of cancer. We also highlight the potential value of targeting FAP to improve current diagnostic and therapeutic approaches.


Subject(s)
Gelatinases , Neoplasms , Fibroblasts/metabolism , Gelatinases/metabolism , Humans , Membrane Proteins/metabolism , Neoplasms/diagnostic imaging , Neoplasms/therapy , Serine Endopeptidases/metabolism
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