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Transactivation of Epidermal Growth Factor Receptor by G Protein-Coupled Receptors: Recent Progress, Challenges and Future Research.
- Source :
-
International journal of molecular sciences [Int J Mol Sci] 2016 Jan 12; Vol. 17 (1). Date of Electronic Publication: 2016 Jan 12. - Publication Year :
- 2016
-
Abstract
- Both G protein-coupled receptors (GPCRs) and receptor-tyrosine kinases (RTKs) regulate large signaling networks, control multiple cell functions and are implicated in many diseases including various cancers. Both of them are also the top therapeutic targets for disease treatment. The discovery of the cross-talk between GPCRs and RTKs connects these two vast signaling networks and complicates the already complicated signaling networks that regulate cell signaling and function. In this review, we focus on the transactivation of epidermal growth factor receptor (EGFR), a subfamily of RTKs, by GPCRs. Since the first report of EGFR transactivation by GPCR, significant progress has been made including the elucidation of the mechanisms underlying the transactivation. Here, we first provide a basic picture for GPCR, EGFR and EGFR transactivation by GPCR. We then discuss the progress made in the last five years and finally provided our view of the future challenge and future researches needed to overcome these challenges.
- Subjects :
- Animals
Cell Line
Endothelin-1 pharmacology
ErbB Receptors metabolism
Fibroblasts cytology
Fibroblasts drug effects
Fibroblasts metabolism
Humans
Lysophospholipids pharmacology
Rats
Receptors, G-Protein-Coupled agonists
Receptors, G-Protein-Coupled metabolism
Signal Transduction
Thrombin pharmacology
ErbB Receptors genetics
Receptor Cross-Talk
Receptors, G-Protein-Coupled genetics
Transcriptional Activation
Subjects
Details
- Language :
- English
- ISSN :
- 1422-0067
- Volume :
- 17
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- International journal of molecular sciences
- Publication Type :
- Academic Journal
- Accession number :
- 26771606
- Full Text :
- https://doi.org/10.3390/ijms17010095