Target Name: SLC2A3
NCBI ID: G6515
Review Report on SLC2A3 Target / Biomarker Content of Review Report on SLC2A3 Target / Biomarker
SLC2A3
Other Name(s): glucose transporter type 3, brain | Solute carrier family 2, facilitated glucose transporter member 3 | Glucose transporter type 3, brain | Solute carrier family 2 member 3 | solute carrier family 2 member 3 | solute carrier family 2 (facilitated glucose transporter), member 3 | GTR3_HUMAN | Solute carrier family 2 (facilitated glucose transporter), member 3 | GLUT-3 | GLUT3

SLC2A3: A Glucose Transporter Type 3 and Potential Drug Target for the Treatment of Diabetes

Abstract:

SLC2A3, also known as glucose transporter type 3, is a protein that plays a crucial role in glucose metabolism and has been linked to the development and progression of type 2 diabetes. This gene has been identified as a potential drug target for the treatment of diabetes , and various studies have suggested that modulating SLC2A3 activity could be a promising strategy for the prevention and management of this disease. In this article, we will review the current understanding of SLC2A3 and its role in diabetes, as well as the potential implications of targeting this protein for therapeutic intervention.

Introduction:

Glucose transporter type 3 (SLC2A3) is a member of the SLC2A family of transporters, which are responsible for transporting various types of molecules across cell membranes. SLC2A3 is specifically involved in the transport of glucose, which is a crucial energy source for the brain. Therefore, alterations in SLC2A3 function have been implicated in various neurological and metabolic disorders, including diabetes.

SLC2A3 is expressed in various tissues throughout the body, including the brain, pancreas, and peripheral tissues. It is highly co-expressed with the transporter GLUT1, which is known to play a complementary role in glucose transport. In addition, SLC2A3 is also co -expressed with the transcription factor PDXP-L1, which has been shown to promote SLC2A3 expression andglucose uptake in pancreatic beta-cells.

SLC2A3 has been linked to the development and progression of type 2 diabetes. Several studies have shown that individuals with the SLC2A3 genotype are more likely to develop type 2 diabetes compared to those without the genotype. Additionally, modulation of SLC2A3 expression has been shown to improve insulin sensitivity and glucose tolerance in individuals with type 2 diabetes.

Targeting SLC2A3 for therapeutic intervention:

SLC2A3 is a protein that has been identified as a potential drug target for the treatment of diabetes. Several studies have shown that modulating SLC2A3 activity can improve insulin sensitivity and glucose tolerance in individuals with type 2 diabetes.

One approach to targeting SLC2A3 is to use small molecules that can modulate its expression or function. One such class of molecules is called agonists, which are molecules that bind to a specific protein with high affinity and prevent it from interacting with its ligand. Agonists have has been shown to be effective in modulating SLC2A3 expression in various tissues, including pancreatic beta-cells and skeletal muscles.

Another approach to targeting SLC2A3 is to use antibodies that can specifically bind to SLC2A3 and prevent it from participating in glucose transport. This approach has been shown to be effective in improving insulin sensitivity and glucose tolerance in individuals with type 2 diabetes.

In addition to these approaches, genetic modulation is also a promising therapeutic strategy. Several studies have shown that individuals with certain genetic variants, such as the SLC2A3 genotype, are more likely to develop type 2 diabetes. Therefore, targeting SLC2A3 with drugs or therapies that modify its expression or function could be a promising strategy for the prevention and management of diabetes.

Conclusion:

SLC2A3 is a protein that has been linked to the development and progression of type 2 diabetes. This protein plays a crucial role in glucose metabolism and has been shown to be involved in various neurological and metabolic disorders. Therefore, modulating SLC2A3 activity could be a promising strategy for the prevention and management of diabetes. Several studies have shown that SLC2A3 can be effectively modulated with small molecules, antibodies, and genetic modulation, and further research is needed to determine its full potential as a therapeutic target

Protein Name: Solute Carrier Family 2 Member 3

Functions: Facilitative glucose transporter that can also mediate the uptake of various other monosaccharides across the cell membrane (PubMed:9477959, PubMed:26176916). Mediates the uptake of glucose, 2-deoxyglucose, galactose, mannose, xylose and fucose, and probably also dehydroascorbate (PubMed:9477959, PubMed:26176916). Does not mediate fructose transport (PubMed:9477959, PubMed:26176916)

The "SLC2A3 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 SLC2A3 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

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