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GPCRs: Emerging anti-cancer drug targets
- Source :
- Cellular signalling. 41
- Publication Year :
- 2017
-
Abstract
- G protein-coupled receptors (GPCRs) constitute the largest and most diverse protein family in the human genome with over 800 members identified to date. They play critical roles in numerous cellular and physiological processes, including cell proliferation, differentiation, neurotransmission, development and apoptosis. Consequently, aberrant receptor activity has been demonstrated in numerous disorders/diseases, and as a result GPCRs have become the most successful drug target class in pharmaceuticals treating a wide variety of indications such as pain, inflammation, neurobiological and metabolic disorders. Many independent studies have also demonstrated a key role for GPCRs in tumourigenesis, establishing their involvement in cancer initiation, progression, and metastasis. Given the growing appreciation of the role(s) that GPCRs play in cancer pathogenesis, it is surprising to note that very few GPCRs have been effectively exploited in pursuit of anti-cancer therapies. The present review provides a broad overview of the roles that various GPCRs play in cancer growth and development, highlighting the potential of pharmacologically modulating these receptors for the development of novel anti-cancer therapeutics.
- Subjects :
- 0301 basic medicine
Protein family
Antineoplastic Agents
Biology
Bioinformatics
Metastasis
Receptors, G-Protein-Coupled
Cancer pathogenesis
03 medical and health sciences
Mice
0302 clinical medicine
Neoplasms
Drug Discovery
medicine
Animals
Humans
Molecular Targeted Therapy
Receptor
G protein-coupled receptor
Drug discovery
Cancer
Cell Biology
medicine.disease
Gene Expression Regulation, Neoplastic
030104 developmental biology
030220 oncology & carcinogenesis
Anti cancer drugs
Disease Progression
Neuroscience
Subjects
Details
- ISSN :
- 18733913
- Volume :
- 41
- Database :
- OpenAIRE
- Journal :
- Cellular signalling
- Accession number :
- edsair.doi.dedup.....d931ce70d0ece76f24a07fd99709b2af