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The clinical relevance of the adhesion G protein-coupled receptor F5 for human diseases and cancers.
Jacenik, Damian; Hikisz, Pawel; Beswick, Ellen J; Fichna, Jakub.
Afiliación
  • Jacenik D; Department of Cytobiochemistry, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, Poland. Electronic address: damian.jacenik@biol.uni.lodz.pl.
  • Hikisz P; Department of Oncobiology and Epigenetics, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, Poland. Electronic address: pawel.hikisz@biol.uni.lodz.pl.
  • Beswick EJ; Division of Gastroenterology, Department of Internal Medicine, University of Kentucky, Lexington, KY, United States. Electronic address: ebeswick@gmail.com.
  • Fichna J; Department of Biochemistry, Faculty of Medicine, Medical University of Lodz, Lodz, Poland. Electronic address: jakub.fichna@umed.lodz.pl.
Biochim Biophys Acta Mol Basis Dis ; 1869(5): 166683, 2023 06.
Article en En | MEDLINE | ID: mdl-36878303
ABSTRACT
Among the numerous adhesion G protein-coupled receptors (GPCRs), adhesion G protein-coupled estrogen receptor F5 (ADGRF5) contains unique domains in the long N-terminal tail which can determine cell-cell and cell-matrix interaction as well as cell adhesion. Nevertheless, the biology of ADGRF5 is complex and still poorly explored. Accumulating evidence suggests that the ADGRF5 activity is fundamental in health and disease. For instance, ADGRF5 is essential in the proper function of lungs and kidney as well as the endocrine system, and its signification in vascularization and tumorigenesis has been demonstrated. The most recent studies have provided findings about the diagnostic potential of ADGRF5 in osteoporosis and cancers, and ongoing studies suggest other diseases as well. Here, we elaborate on the current state of knowledge about the ADGRF5 in the physiology and pathophysiology of human diseases and highlight its high potential as a novel target in various therapeutic areas.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Relevancia Clínica / Neoplasias Límite: Humans Idioma: En Revista: Biochim Biophys Acta Mol Basis Dis Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Relevancia Clínica / Neoplasias Límite: Humans Idioma: En Revista: Biochim Biophys Acta Mol Basis Dis Año: 2023 Tipo del documento: Article