Target Name: GLA
NCBI ID: G2717
Review Report on GLA Target / Biomarker Content of Review Report on GLA Target / Biomarker
GLA
Other Name(s): alpha-galactosidase A | alpha-D-galactoside galactohydrolase | GALA | agalsidase alfa | Alpha-D-galactoside galactohydrolase | Alpha-gal A | Agalsidase | melibiase | alpha-D-galactosidase A | Agalsidase alfa | Alpha-D-galactoside galactohydrolase 1 | alpha-D-galactoside galactohydrolase 1 | galactosidase alpha | alpha-gal A | Alpha-galactosidase A | Melibiase | GLA variant 1 | Alpha-D-galactosidase A | galactosylgalactosylglucosylceramidase GLA | Galactosidase alpha, transcript variant 1 | Galactosylgalactosylglucosylceramidase GLA | AGAL_HUMAN

GLA as A Drug Target Or Biomarker: Potential and Mechanisms

GLA (alpha-galactosidase A) is a protein that is expressed in most tissues of the body. It is a key enzyme in the glycosylation process, which is the final step in the breakdown of carbohydrates by the body. GLA is also involved in the development and maintenance of the extracellular matrix (ECM), which is a complex tissue matrix that provides support and structure to various body systems.

Recent studies have suggested that GLA may have potential as a drug target or biomarker. One of the main reasons for this is the fact that GLA has been shown to play a role in the development and progression of various diseases, including cancer, neurodegenerative diseases, and autoimmune disorders.

In addition, GLA has also been shown to be involved in several cellular processes that are important for human health, including cell signaling, angiogenesis, and fibrosis. This suggests that targeting GLA may be a promising way to treat a variety of diseases that are currently difficult to treat.

One of the key advantages of targeting GLA is its potential to disrupt the formation of the ECM, which is a complex tissue matrix that is involved in many important physiological processes in the body. The ECM is made up of a variety of proteins that work together to provide support and structure to various body systems, including the skin, bones, and connective tissues.

In diseases such as cancer, the ECM provides a supportive environment for tumor cells to grow and evolve. Similarly, in neurodegenerative diseases such as Alzheimer's disease, the accumulation of beta-amyloid peptides in the ECM has been shown to contribute to the development and progression of the disease.

Targeting GLA may be a way to disrupt the formation of the ECM and potentially treat these diseases. One approach that is being explored is the use of small molecules, such as drugs that bind to GLA, to disrupt the formation of the ECM. This could involve targeting specific regions of GLA that are involved in the formation of the ECM, or targeting GLA broadly to disrupt its overall function.

Another potential mechanism by which GLA may contribute to the development and progression of diseases is its role in cell signaling. GLA has been shown to play a role in the regulation of cell signaling pathways, including the TGF-beta pathway. This pathway is involved in the regulation of cell growth, differentiation, and survival, and is a key factor in the development and progression of many diseases.

Targeting GLA may be a way to disrupt the TGF-beta pathway and potentially treat diseases that are caused by its activity. For example, one approach being explored is the use of small molecules that bind to GLA and disrupt its function in the TGF-beta pathway. This could involve targeting specific regions of GLA that are involved in the TGF-beta pathway, or targeting GLA broadly to disrupt its overall function.

In addition, GLA has also been shown to play a role in the regulation of angiogenesis, which is the process by which new blood vessels are formed. This suggests that targeting GLA may be a way to disrupt the angiogenic process and potentially treat diseases that are caused by its activity.

Targeting GLA may also be a way to treat diseases that are caused by its accumulation in the ECM. For example, one approach being explored is the use of small molecules that bind to GLA and disrupt its function in the formation of the ECM. This could involve targeting specific regions of GLA that are involved in the formation of the ECM, or targeting GLA broadly to disrupt its overall function.

Overall, GLA is a protein that has been shown to play a role in several important cellular processes that are involved in human health. Targeting GLA may be a promising way to treat a variety of diseases that are currently difficult to treat. Further research is needed to

Protein Name: Galactosidase Alpha

Functions: Catalyzes the hydrolysis of glycosphingolipids and participates in their degradation in the lysosome

The "GLA 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 GLA 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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GLB1 | GLB1L | GLB1L2 | GLB1L3 | GLC1C | GLCCI1 | GLCCI1-DT | GLCE | GLDC | GLDN | GLE1 | GLG1 | GLI1 | GLI2 | GLI3 | GLI4 | GLIDR | GLIPR1 | GLIPR1L1 | GLIPR1L2 | GLIPR2 | GLIS1 | GLIS2 | GLIS3 | GLIS3-AS1 | GLMN | GLMP | GLO1 | GLOD4 | GLOD5 | GLP1R | GLP2R | GLRA1 | GLRA2 | GLRA3 | GLRA4 | GLRB | GLRX | GLRX2 | GLRX3 | GLRX3P2 | GLRX5 | GLS | GLS2 | GLT1D1 | GLT6D1 | GLT8D1 | GLT8D2 | GLTP | GLTPD2 | Glucagon-like peptide receptor (GLP-R) | Glucosidase | GLUD1 | GLUD1P2 | GLUD1P3 | GLUD2 | GLUL | GLULP2 | GLULP4 | Glutamate receptor | Glutamate Receptor Ionotropic | Glutamate Receptor Ionotropic AMPA Receptor | Glutamate Transporter | Glutaminase | Glutathione peroxidase | Glutathione S-Transferase (GST) | GLYAT | GLYATL1 | GLYATL1B | GLYATL2 | GLYATL3 | GLYCAM1 | Glycine receptor | Glycogen phosphorylase | Glycogen synthase | Glycogen synthase kinase 3 (GSK-3) | Glycoprotein hormone | Glycoprotein Hormone Receptor | GLYCTK | Glycylpeptide N-tetradecanoyltransferase | Glypican | GLYR1 | GM-CSF Receptor (GM-CSF-R) | GM1 ganglioside | GM2A | GM2AP1 | GM2AP2 | GMCL1 | GMCL2 | GMDS | GMDS-DT | GMEB1 | GMEB2 | GMFB | GMFG | GMIP | GML | GMNC | GMNN | GMPPA