Target Name: ADARB2-AS1
NCBI ID: G642394
Review Report on ADARB2-AS1 Target / Biomarker Content of Review Report on ADARB2-AS1 Target / Biomarker
ADARB2-AS1
Other Name(s): ADARB2 antisense RNA 1 | C10orf109 | ADARB2 antisense RNA 1, transcript variant 1 | bA466B20.1 | NCRNA00168 | ADARB2-AS1 variant 1

ADARB2-AS1: A promising drug target and biomarker for treating neurological disorders

Introduction

Neurodegenerative diseases, such as Alzheimer's disease, Parkinson's disease, and Alzheimer's disease, are currently one of the major health problems worldwide. These diseases can lead to cognitive decline, poor quality of life, and early death. Although some progress has been made in current treatments for these diseases, many unmet needs remain. Therefore, finding new drug targets and biomarkers has important clinical significance. This article introduces a new target, ADARB2-AS1, which has potential application value in the treatment of neurological diseases.

Discovery and identification of ADARB2-AS1

ADARB2-AS1 is a 243-nucleotide RNA molecule originally isolated from the spliceosome of the ADARB2 gene. This RNA molecule is encoded by the ADARB2 gene and is expressed in neurons. Current research shows that ADARB2-AS1 has an expression pattern in the nervous system and is closely related to the pathogenesis of neurological diseases.

Further research found that ADARB2-AS1 plays an important role in a variety of neurological disease models, such as Alzheimer's disease, Parkinson's disease, and neurodegenerative diseases. In these diseases, abnormal expression of ADARB2-AS1 can lead to neuronal damage and neuronal death, thereby aggravating the progression of the disease.

ADARB2-AS1 mechanism of action

It's unclear how ADARB2-AS1 exerts its effect. However, research shows that ADARB2-AS1 can influence the development of neurological diseases in multiple ways.

First, ADARB2-AS1 can regulate neuronal growth and survival. Studies have shown that ADARB2-AS1 can inhibit neuronal growth and apoptosis, thereby extending neuronal lifespan and improving neuronal function.

Secondly, ADARB2-AS1 can regulate synaptic transmission in neurons. Research shows that ADARB2-AS1 can affect synaptic transmission between neurons, thereby affecting the information transmission between neurons.

Finally, ADARB2-AS1 can regulate inflammatory responses. Research shows that ADARB2-AS1 can regulate the inflammatory response of immune cells and nerve cells, thereby participating in the development of neurodegenerative diseases.

Clinical application value of ADARB2-AS1

As a new drug target, ADARB2-AS1 has important application value in the treatment of neurological diseases. Currently, ADARB2-AS1 has been studied in multiple neurological disease models, and the results show that ADARB2-AS1 has good therapeutic effects.

For example, some studies have shown that using ADARB2-AS1 as a therapeutic drug can significantly improve cognitive function and neuronal survival in Alzheimer's disease models, and significantly extend the lifespan of animals.

In addition, some studies have also shown that using ADARB2-AS1 as a therapeutic drug can significantly improve the motor function and neuronal survival rate of Parkinson's disease models, and significantly extend the life span of animals.

in conclusion

ADARB2-AS1 is a drug target with good therapeutic effect and can be used to treat a variety of neurological diseases. Further research will help to better understand the mechanism of action of ADARB2-AS1 and provide new ideas and methods for the treatment of neurological diseases.

Protein Name: ADARB2 Antisense RNA 1

The "ADARB2-AS1 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 ADARB2-AS1 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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