Target Name: FFAR1
NCBI ID: G2864
Review Report on FFAR1 Target / Biomarker Content of Review Report on FFAR1 Target / Biomarker
FFAR1
Other Name(s): FFA1R | Free fatty acid receptor 1 | G-protein coupled receptor 40 | GPCR40 | SNORF55 | FFAR1_HUMAN | free fatty acid receptor 1 | G protein-coupled receptor 40 | GPR40

FFAR1 as A Potential Drug Target and Biomarker

FFA1R (Farnesyl-F-1-alpha-ketoglutarate reductase), also known as FFAR1, is a protein that is expressed in various tissues throughout the body. It is a key enzyme in the fatty acid biosynthesis pathway, which is a critical pathway for the production of essential fatty acids (EFAs) in the body. FFAR1 plays a crucial role in the production of these fatty acids, particularly arachidonic acid, which is a key component of cell membranes and has various physiological functions.

Drug Target and Biomarker

FFAR1 has been identified as a potential drug target for several diseases, including cardiovascular disease, neurodegenerative diseases, and autoimmune diseases. The high levels of FFAR1 expression in certain diseases, such as cancer, have also led to its potential as a biomarker for disease diagnosis and prognosis.

One of the main reasons for the potential of FFAR1 as a drug target is its involvement in various signaling pathways. FFAR1 is a key enzyme in the PI3K/Akt signaling pathway, which is involved in the regulation of cell growth, survival, and angiogenesis. This pathway has been implicated in the development and progression of many diseases, including cancer, neurodegenerative diseases, and cardiovascular disease.

In addition to its involvement in the PI3K/Akt signaling pathway, FFAR1 is also involved in the regulation of cell adhesion and migration. This is important for the development of tissues and organs, including blood vessels, neurons, and muscles.

FFAR1 has also been shown to be involved in the regulation of inflammation and immune responses. Its expression has been observed in various immune cells, including T cells, and its involvement in the production of pro-inflammatory cytokines has been implicated in the development of autoimmune diseases.

Targeting FFAR1

The development of small molecules that can specifically target FFAR1 has the potential to be a valuable tool for the treatment of diseases associated with high levels of FFAR1 expression, including cardiovascular disease, neurodegenerative diseases, and autoimmune diseases.

One approach to targeting FFAR1 is the use of inhibitors of the PI3K/Akt signaling pathway. These inhibitors can be used to reduce the levels of FFAR1 in cancer cells, which could lead to a reduction in the production of arachidonic acid and its associated risk for disease.

Another approach to targeting FFAR1 is the use of small molecules that specifically modulate the activity of FFAR1. These small molecules can be used to either activate or inhibit the activity of FFAR1, depending on the desired effect on the body.

FFAR1 as a Biomarker

FFAR1 has been shown to be a valuable biomarker for several diseases, including cancer. Its high levels of expression in cancer cells have been associated with a poor prognosis and increased risk of disease.

One approach to using FFAR1 as a biomarker is to measure its levels in cancer cells or body fluids, such as blood or urine. This can be done using techniques such as qRT-PCR, a sensitive technique for the detection of RNA, or mass spectrometry , which is a more sensitive technique for the detection of proteins.

Another approach to using FFAR1 as a biomarker is to measure its levels in body fluids or tissues. This can be done using techniques such as enzyme immunoprecipitation or protein array analysis.

Conclusion

FFAR1 is a protein that is involved in the production of essential fatty acids and has been identified as a potential drug target for several diseases, including cardiovascular disease, neurodegenerative diseases, and autoimmune diseases. Its involvement in various signaling pathways and its high levels of expression in certain diseases make it an attractive target for small molecules that can specifically modulate its activity. Further research is needed to fully understand the role of FFAR1 as a biomarker

Protein Name: Free Fatty Acid Receptor 1

Functions: G-protein coupled receptor for medium and long chain saturated and unsaturated fatty acids that plays an important role in glucose homeostasis. Fatty acid binding increases glucose-stimulated insulin secretion, and may also enhance the secretion of glucagon-like peptide 1 (GLP-1). May also play a role in bone homeostasis; receptor signaling activates pathways that inhibit osteoclast differentiation (By similarity). Ligand binding leads to a conformation change that triggers signaling via G-proteins that activate phospholipase C, leading to an increase of the intracellular calcium concentration. Seems to act through a G(q) and G(i)-mediated pathway. Mediates the anti-inflammatory effects of omega-3 polyunsaturated fatty acids (PUFAs) via inhibition of NLRP3 inflammasome activation

The "FFAR1 Target / Biomarker Review Report" is a customizable review of hundreds up to thousends of related scientific research literature by AI technology, covering specific information about FFAR1 comprehensively, including but not limited to:
•   general information;
•   protein structure and compound binding;
•   protein biological mechanisms;
•   its importance;
•   the target screening and validation;
•   expression level;
•   disease relevance;
•   drug resistance;
•   related combination drugs;
•   pharmacochemistry experiments;
•   related patent analysis;
•   advantages and risks of development, etc.
The report is helpful for project application, drug molecule design, research progress updates, publication of research papers, patent applications, etc. If you are interested to get a full version of this report, please feel free to contact us at BD@silexon.ai

More Common Targets

FFAR2 | FFAR3 | FFAR4 | FGA | FGB | FGD1 | FGD2 | FGD3 | FGD4 | FGD5 | FGD5-AS1 | FGD5P1 | FGD6 | FGF1 | FGF10 | FGF10-AS1 | FGF11 | FGF12 | FGF12-AS2 | FGF13 | FGF13-AS1 | FGF14 | FGF14-AS1 | FGF14-AS2 | FGF14-IT1 | FGF16 | FGF17 | FGF18 | FGF19 | FGF2 | FGF20 | FGF21 | FGF22 | FGF23 | FGF3 | FGF4 | FGF5 | FGF6 | FGF7 | FGF7P3 | FGF7P5 | FGF7P6 | FGF8 | FGF9 | FGFBP1 | FGFBP2 | FGFBP3 | FGFR1 | FGFR1OP2 | FGFR2 | FGFR3 | FGFR3P1 | FGFR4 | FGFRL1 | FGG | FGGY | FGL1 | FGL2 | FGR | FH | FHAD1 | FHDC1 | FHF Complex | FHIP1A | FHIP1B | FHIP2A | FHIP2B | FHIT | FHL1 | FHL2 | FHL3 | FHL5 | FHOD1 | FHOD3 | FIBCD1 | FIBIN | FIBP | Fibrinogen | Fibroblast growth factor (FGF) | Fibroblast Growth Factor Receptor (FGFR) | Fibronectin Type III Domain | FICD | FIG4 | FIGLA | FIGN | FIGNL1 | FIGNL2 | FILIP1 | FILIP1L | FILNC1 | FIP1L1 | FIRRE | FIS1 | FITM1 | FITM2 | Five friends of methylated CHTOP complex | FIZ1 | FJX1 | FKBP10 | FKBP11