GCPII and its close homolog GCPIII: from a neuropeptidase to a cancer marker and beyond
Jazyk angličtina Země Singapur Médium electronic
Typ dokumentu časopisecké články, práce podpořená grantem, přehledy
PubMed
30844704
DOI
10.2741/4742
PII: 4742
Knihovny.cz E-zdroje
- MeSH
- adenokarcinom metabolismus MeSH
- antigeny povrchové metabolismus MeSH
- fenotyp MeSH
- glutamátkarboxypeptidasa II metabolismus MeSH
- glutamáty chemie MeSH
- hydrolýza MeSH
- idiopatické střevní záněty metabolismus MeSH
- jejunum metabolismus MeSH
- karboxypeptidasy metabolismus MeSH
- krysa rodu Rattus MeSH
- kyselina asparagová analogy a deriváty chemie MeSH
- lidé MeSH
- modely nemocí na zvířatech MeSH
- monoklonální protilátky chemie MeSH
- mozek metabolismus MeSH
- mutantní kmeny myší MeSH
- myši transgenní MeSH
- myši MeSH
- nádorové biomarkery metabolismus MeSH
- nádory prostaty metabolismus MeSH
- neuropeptidy chemie MeSH
- proteasy metabolismus MeSH
- tenké střevo metabolismus MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- lidé MeSH
- mužské pohlaví MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- přehledy MeSH
- Názvy látek
- antigeny povrchové MeSH
- FOLH1 protein, human MeSH Prohlížeč
- glutamátkarboxypeptidasa II MeSH
- glutamáty MeSH
- karboxypeptidasy MeSH
- kyselina asparagová MeSH
- monoklonální protilátky MeSH
- N-acetylaspartate MeSH Prohlížeč
- N-acetylglutamic acid MeSH Prohlížeč
- NAALAD2 protein, human MeSH Prohlížeč
- nádorové biomarkery MeSH
- neuropeptidy MeSH
- proteasy MeSH
Glutamate carboxypeptidases II and III (GCPII and GCPIII) are highly homologous di-zinc metallopeptidases belonging to the M28 family. These enzymes are expressed in a variety of tissues, including the brain, prostate, kidney, testis and jejunum. GCPII has been recognized as a neuropeptidase in the central nervous system, as a folate hydrolase participating in absorption of folates in the jejunum and, most importantly, as a prostate-specific membrane antigen that is highly expressed in prostate adenocarcinoma. Furthermore, it has been identified in the neovasculature of most human solid tumors. In contrast, GCPIII has not been associated with any specific physiological function or pathology, and its expression, activity and inhibition have not been as well-studied. In this review, we provide an overview of the current understanding of the structure, enzymatic activity, substrate specificity, and tissue distribution of these two homologous enzymes. We discuss their potential physiological functions and describe the available animal models, including genetically modified mice. We also review the potential use of specific monoclonal antibodies and small-molecule inhibitors recognizing GCPII/III for diagnosis, imaging and experimental therapy of human cancers and other pathologies.
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