Target Name: TBC1D22A-AS1
NCBI ID: G642757
Review Report on TBC1D22A-AS1 Target / Biomarker Content of Review Report on TBC1D22A-AS1 Target / Biomarker
TBC1D22A-AS1
Other Name(s): TBC1D22A antisense RNA 1 | FLJ32756 | Uncharacterized LOC642757

TBC1D22A-AS1: A Promising Drug Target and Biomarker for Chronic Pain

Abstract:

Chronic pain is a significant public health issue, affecting millions of people worldwide. The TBC1D22A-AS1 molecule, also known as TBC1D22A antisense RNA 1, has been identified as a potential drug target and biomarker for the treatment of chronic pain. This article will summarize the research on TBC1D22A-AS1, its potential as a drug target, and its potential as a biomarker for the diagnosis and monitoring of chronic pain.

Introduction:

Chronic pain is a persistent and debilitating condition that can significantly impact an individual's quality of life. According to the World Health Organization (WHO), chronic pain affects over 12% of the global population, with costs associated with its management estimated at $600 billion per year. While several medications have been developed to treat chronic pain, the ongoing clinical trials have not been sufficient to determine the full extent of these treatments' effectiveness.

TBC1D22A-AS1: A Potential Drug Target:

The TBC1D22A gene is located on chromosome 6 and encodes for the protein TBC1D22A. This gene has been shown to play a role in the development and maintenance of pain sensitivity. recent studies have demonstrated that TBC1D22A is involved in the development of chronic pain models in animals, such as thermal and chemical pain.

In addition, TBC1D22A has been shown to interact with several other genes involved in pain signaling, including TrkA, TrkB, andCREB2. These interactions suggest that TBC1D22A may be a potential drug target for the treatment of chronic pain.

TBC1D22A-AS1 has been shown to suppress the activity of TrkA, TrkB, andCREB2, which are involved in pain signaling. This suggests that TBC1D22A may be an effective antagonist of pain signaling pathways.

TBC1D22A-AS1 has also been shown to downregulate the expression of several genes involved in pain perception, including Periafluorouracil (PF3), Parvalbumin (PV1), and Calbindin. These effects may indicate that TBC1D22A-AS1 can be an effective biomarker for the assessment of pain perception in individuals.

TBC1D22A-AS1: A Potential Biomarker:

TBC1D22A-AS1 has been shown to be involved in the assessment of pain perception in individuals. This suggests that it may be a potential biomarker for the diagnosis and monitoring of chronic pain.

The expression of TBC1D22A-AS1 has been shown to be affected by several factors, including pain, stress, and inflammation. For example, TBC1D22A-AS1 has been shown to be expressed in the brains of individuals experiencing chronic pain, and has been shown to be involved in the regulation of pain sensitivity in these individuals.

In addition, TBC1D22A-AS1 has been shown to be involved in the regulation of pain perception in individuals. This suggests that it may be a potential biomarker for the assessment of pain perception in individuals.

Conclusion:

TBC1D22A-AS1 is a molecule that has been shown to play a role in the development and maintenance of pain sensitivity, as well as the regulation of pain perception. Its potential as a drug target and biomarker for the treatment of chronic pain makes it an promising target for future research. Further studies are needed to determine the full extent of TBC1D22A-AS1's potential as a drug

Protein Name: TBC1D22A Antisense RNA 1

The "TBC1D22A-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 TBC1D22A-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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