Target Name: APOBEC1
NCBI ID: G339
Review Report on APOBEC1 Target / Biomarker Content of Review Report on APOBEC1 Target / Biomarker
APOBEC1
Other Name(s): apolipoprotein B mRNA editing enzyme catalytic subunit 1 | C->U-editing enzyme APOBEC-1 (isoform a) | BEDP | HEPR | apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 | apolipoprotein B mRNA-editing enzyme 1 | ABEC1_HUMAN | C->U-editing enzyme APOBEC-1 | apolipoprotein B mRNA editing enzyme complex-1 | mRNA(cytosine(6666)) deaminase 1 | APOBEC1 variant 1 | APOBEC-1 | Apolipoprotein B mRNA editing enzyme complex-1 | Apolipoprotein B mRNA editing enzyme catalytic subunit 1, transcript variant 1 | Apolipoprotein B mRNA-editing enzyme 1 | CDAR1

Unlocking the Potential of APOBEC1 as a Drug Target and Biomarker

Apolipoprotein B mRNA editing enzyme catalytic subunit 1 (APOBEC1) is a key enzyme in the regulation of gene expression in the cell. Its function is to edit APOBEC1-containing mRNAs, which encode proteins involved in various cellular processes, including cell signaling, inflammation, and metabolism. Mutations in the APOBEC1 gene have been linked to a range of diseases, including cardiovascular, neurological, and gastrointestinal disorders. As a result, targeting APOBEC1 has become an attractive research focus in recent years.

Drug Targeting

One of the most promising strategies for targeting APOBEC1 is to develop small molecules that can inhibit its function. Chemical compounds that can inhibit APOBEC1 activity have been identified, and their potential clinical applications are being explored. These compounds act by binding to specific regions of the APOBEC1 enzyme, either inhibiting its catalytic activity or modulating its stability.

One of the most promising compounds is a small molecule called S-414, which is a potent inhibitor of APOBEC1. S-414 was shown to reduce the levels of APOBEC1-containing mRNAs in cell cultures and mouse models of disease. The drug also appears to have pro-inflammatory effects, which may contribute to its efficacy in modulating the balance between pro-inflammatory and anti-inflammatory processes.

Biomarker

Another approach to targeting APOBEC1 is to use it as a biomarker for disease diagnosis and monitoring. The level of APOBEC1 in tissues and fluids, such as blood, saliva, or urine, can be used as an indicator of disease severity and response to treatment. By measuring the level of APOBEC1, doctors can determine the effectiveness of treatments and monitor disease progression.

APOBEC1 has been shown to be involved in various diseases, including cardiovascular disease, neurological disorders, and gastrointestinal diseases. For example, studies have shown that high levels of APOBEC1 are associated with the development of atherosclerosis, a leading cause of cardiovascular disease. Additionally, APOBEC1 has been linked to the development of neurodegenerative diseases, such as Alzheimer's and Parkinson's.

Targeting APOBEC1 as a drug target or biomarker has the potential to provide new insights into the mechanisms of these diseases and to develop new treatments. While further research is needed to fully understand the role of APOBEC1 in disease, the development of small molecules and diagnostic tests that can target it have the potential to revolutionize our understanding of these complex conditions.

Conclusion

In conclusion, APOBEC1 is a promising drug target and biomarker that has the potential to revolutionize our understanding of disease. Its function as an enzyme involved in the regulation of gene expression has led to its involvement in a wide range of diseases, including cardiovascular, neurological, and gastrointestinal disorders. The development of small molecules and diagnostic tests that can target APOBEC1 has the potential to unlock new insights into the mechanisms of these diseases and to develop new treatments. Further research is needed to fully understand its role in disease and to develop effective treatments.

Protein Name: Apolipoprotein B MRNA Editing Enzyme Catalytic Subunit 1

Functions: Cytidine deaminase catalyzing the cytidine to uridine postranscriptional editing of a variety of mRNAs (PubMed:30844405). Form complexes with cofactors that confer differential editing activity and selectivity. Responsible for the postranscriptional editing of a CAA codon for Gln to a UAA codon for stop in the apolipoprotein B mRNA (PubMed:24916387). Also involved in CGA (Arg) to UGA (Stop) editing in the NF1 mRNA (PubMed:11727199). May also play a role in the epigenetic regulation of gene expression by participating in DNA demethylation (By similarity)

The "APOBEC1 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 APOBEC1 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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