Target Name: MIR4468
NCBI ID: G100616226
Review Report on MIR4468 Target / Biomarker Content of Review Report on MIR4468 Target / Biomarker
MIR4468
Other Name(s): MicroRNA 4468 | microRNA 4468 | hsa-miR-4468 | hsa-mir-4468

MIR4468: A Potential Drug Target and Biomarker for the Treatment of Chronic Pain

Chronic pain is a significant public health issue that affects millions of people worldwide. According to the World Health Organization (WHO), chronic pain costs the global economy approximately 63 billion dollars per year, which represents over 10% of global healthcare expenditure. Additionally, chronic pain can significantly reduce quality of life, leading to significant physical, emotional, and social consequences.

Recent studies have identified several potential drug targets and biomarkers for the treatment of chronic pain. MIR4468, a non-coding RNA molecule, has been identified as a potential drug target and biomarker for the treatment of chronic pain. In this article, we will discuss the potential mechanisms of MIR4468 as a drug target and biomarker for the treatment of chronic pain.

Mechanisms of MIR4468 as a Drug Target

MIR4468 is a non-coding RNA molecule that is expressed in various tissues and cells in the body. It is a key regulator of gene expression and has been involved in the regulation of pain signaling pathways. MIR4468 has been shown to play a role in the regulation of nociceitone gene expression, which is a key mediator of pain signaling.

Studies have shown that MIR4468 can inhibit the activity of nociceitone, a potent pain mediator, and prevent the development of pain. Additionally, MIR4468 has been shown to enhance the activity of a potential pain modulator, U012647, which can inhibit the production of nociceitone and decrease pain.

MIR4468 has also been shown to play a role in the regulation of pain modulation by the endogenous opioid system. Studies have shown that MIR4468 can bind to the opioid receptor and modulate the activity of opioids such as U012647 and Fentanyl. This suggests that MIR4468 may be a potential drug target for the treatment of chronic pain associated with opioid use disorders.

Mechanisms of MIR4468 as a Biomarker

MIR4468 has also been shown to be a potential biomarker for the diagnosis and monitoring of chronic pain. Studies have shown that MIR4468 levels are significantly decreased in individuals with chronic pain, and that MIR4468 levels can be used as a biomarker to monitor the effectiveness of pain treatments.

In addition, MIR4468 has been shown to be involved in the regulation of pain processing in the brain. Studies have shown that MIR4468 is expressed in the central nervous system and is involved in the regulation of pain processing in the brain. This suggests that MIR4468 may be a potential biomarker for the diagnosis and treatment of chronic pain.

Conclusion

MIR4468 is a non-coding RNA molecule that has been shown to play a role in the regulation of pain signaling pathways. Its potential as a drug target and biomarker for the treatment of chronic pain makes it an attractive target for further research. Further studies are needed to fully understand the mechanisms of MIR4468 as a drug target and biomarker for the treatment of chronic pain.

Protein Name: MicroRNA 4468

The "MIR4468 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 MIR4468 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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