Target Name: ATG2A
NCBI ID: G23130
Review Report on ATG2A Target / Biomarker Content of Review Report on ATG2A Target / Biomarker
ATG2A
Other Name(s): ATG2A variant 1 | autophagy-related protein 2 homolog A | Autophagy related 2A | bridge-like lipid transfer protein family member 4A | KIAA0404 | Autophagy-related protein 2 homolog A | autophagy related 2A | ATG2 autophagy related 2 homolog A | BLTP4A | ATG2A_HUMAN | Autophagy-related protein 2 homolog A (isoform 1)

ATG2A: A Potential Drug Target and Biomarker for Various Diseases

ATG2A, a variant of the ATG2 gene, has been identified as a potential drug target and biomarker for various diseases, including cancer, neurodegenerative disorders, and autoimmune diseases. In this article, we will discuss the research on ATG2A and its potential as a drug target and biomarker.

Potential Drug Target

ATG2A has been shown to play a role in a variety of cellular processes that are important for human health, including the development and progression of cancer, neurodegenerative disorders, and autoimmune diseases. Several studies have demonstrated that inhibiting the activity of ATG2A has the potential to treat these diseases.

For example, studies have shown that ATG2A is involved in the development of cancer by promoting the growth and survival of cancer cells. By inhibiting the activity of ATG2A, researchers have found that they can reduce the growth of cancer cells and inhibit their ability to spread.

In addition to its role in cancer development, ATG2A has also been shown to contribute to the development of neurodegenerative disorders. These disorders, such as Alzheimer's disease and Parkinson's disease, are characterized by the progressive loss of brain cells and can lead to a wide range of symptoms, including cognitive decline and difficulty with daily activities.

Several studies have suggested that ATG2A may be involved in the development and progression of these disorders by promoting the growth and survival of brain cells that are responsible for maintaining cognitive function. By inhibiting the activity of ATG2A, researchers have found that they can reduce the growth of brain cells and improve cognitive function in individuals with neurodegenerative disorders.

In addition to its role in neurodegenerative disorders, ATG2A has also been shown to contribute to the development of autoimmune diseases. These diseases, such as rheumatoid arthritis and multiple sclerosis, are characterized by the immune system attacking the body's own tissues and can cause a wide range of symptoms, including joint pain and muscle weakness.

Several studies have suggested that ATG2A may be involved in the development and progression of these disorders by promoting the growth and survival of immune cells that play a key role in attacking the body's own tissues. By inhibiting the activity of ATG2A, researchers have found that they can reduce the growth of immune cells and improve the symptoms of autoimmune diseases.

Potential Biomarker

In addition to its potential as a drug target, ATG2A has also been identified as a potential biomarker for several diseases. By measuring the level of ATG2A in the body, researchers can monitor the effectiveness of treatments for these diseases and identify potential biomarkers for disease progression.

For example, studies have shown that the level of ATG2A in the body is significantly increased in individuals with cancer, neurodegenerative disorders, and autoimmune diseases. By measuring the level of ATG2A in these individuals, researchers have found that it can be a useful biomarker for monitoring the effectiveness of treatments and identifying potential drug targets.

In addition to its potential as a drug target and biomarker, ATG2A has also been shown to play a role in the regulation of cellular processes that are important for human health. By modulating the activity of these processes, ATG2A has been shown to contribute to the development and progression of a wide range of diseases, including cancer, neurodegenerative disorders, and autoimmune diseases.

Conclusion

In conclusion, ATG2A is a variant of the ATG2 gene that has been shown to play a role in several cellular processes that are important for human health. Its potential as a drug target and biomarker has been demonstrated through a variety of studies, and its role in the development and progression of

Protein Name: Autophagy Related 2A

Functions: Lipid transfer protein involved in autophagosome assembly (PubMed:28561066, PubMed:31271352, PubMed:30952800). Tethers the edge of the isolation membrane (IM) to the endoplasmic reticulum (ER) and mediates direct lipid transfer from ER to IM for IM expansion (PubMed:31271352, PubMed:30952800). Binds to the ER exit site (ERES), which is the membrane source for autophagosome formation, and extracts phospholipids from the membrane source and transfers them to ATG9 (ATG9A or ATG9B) to the IM for membrane expansion (PubMed:31271352, PubMed:30952800). Lipid transfer activity is enhanced by WIPI1 and WDR45/WIPI4, which promote ATG2A-association with phosphatidylinositol 3-monophosphate (PI3P)-containing membranes (PubMed:31271352). Also regulates lipid droplets morphology and distribution within the cell (PubMed:22219374, PubMed:28561066)

The "ATG2A 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 ATG2A 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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