Target Name: MIR423
NCBI ID: G494335
Review Report on MIR423 Target / Biomarker Content of Review Report on MIR423 Target / Biomarker
MIR423
Other Name(s): mir-423 | hsa-mir-423 | Hsa-mir-423 | hsa-miR-423-5p | MicroRNA 423 | MIRN423 | hsa-miR-423-3p | microRNA 423

MIR423: A Potential Drug Target and Biomarker for Chronic Pain

Chronic pain is a significant public health issue, affecting millions of people worldwide. The World Health Organization (WHO) estimates that 10% of the global population experiences chronic pain, with costs associated with chronic pain reaching $63 billion annually. Chronic pain can be caused by various conditions, including musculoskeletal disorders, neuropsychiatric diseases, and other chronic conditions.

MIR423, a non-coding RNA (ncRNA), has been identified as a potential drug target and biomarker for chronic pain. MIR423 is a key regulator of the uncoupling protein (UCP) gene, which is involved in the function of mitochondria. UCP is a transmembrane protein that plays a crucial role in the regulation of mitochondrial energy metabolism. MIR423 has been shown to regulate the expression of genes involved in pain perception, inflammation, and cellular stress responses.

In this article, we will discuss the potential implications of MIR423 as a drug target and biomarker for chronic pain. We will review the current research on MIR423 and its potential clinical applications, including its potential as a therapeutic drug for chronic pain.

Current Research on MIR423

MIR423 has been shown to play a critical role in the regulation of mitochondrial function and energy metabolism. Several studies have demonstrated that MIR423 regulates the expression of genes involved in pain perception, inflammation, and cellular stress responses.

MIR423 has been shown to regulate the expression of genes involved in the production of pro-inflammatory cytokines, such as TNF-伪 and IL-1尾. MIR423 has also been shown to inhibit the expression of genes involved in the production of anti-inflammatory cytokines, such as IL-10. These findings suggest that MIR423 may have a negative impact on the production of pro-inflammatory cytokines, which are often associated with chronic pain.

MIR423 has also been shown to regulate the expression of genes involved in the production of pain-related genes, such as TrkA and FasL. These findings suggest that MIR423 may be involved in the regulation of pain perception.

MIR423 has also been shown to regulate the expression of genes involved in cellular stress responses, such as Hsp70 and Hsp90. These findings suggest that MIR423 may be involved in the regulation of cellular stress responses, which can contribute to chronic pain.

Potential Clinical Applications of MIR423

MIR423 has been shown to have potential as a therapeutic drug for chronic pain. Several studies have demonstrated that MIR423 may be an effective target for pain relief by modulating the activity of pain-related genes.

One potential clinical application of MIR423 is as a treatment for chronic low back pain (CLBP). CLBP is a common condition that affects millions of people worldwide, with significant economic and social impacts. Several studies have shown that MIR423 may be an effective target for CLBP by modulating the activity of pain-related genes. For example, a study by Li et al. (2020) found that MIR423 was downregulated in the L5 region of the spine, which is often affected by CLBP, and was associated with increased pain perception. Therefore, MIR423 may be an effective target for CLBP by modulating the activity of pain-related genes in the L5 region of the spine.

Another potential clinical application of MIR423 is as a treatment for chronic pain associated with neuropsychiatric diseases, such as depression and anxiety. These conditions can be associated with increased pain perception and can have a significant impact on quality of life. Several studies have shown that MIR423 may be an effective target for neuropsychiatric diseases by modulating the activity of pain-related genes. For example, a study by Zhang et al. (2020) found that MIR423 was downregulated in the hippocampus of individuals with major depressive disorder (MDD) and was associated with increased pain perception. Therefore, MIR423 may be an effective target for neuropsychiatric diseases

Protein Name: MicroRNA 423

The "MIR423 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 MIR423 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

More Common Targets

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