IMPDH2: A Drug Target and Biomarker for Chronic Pain (G3615)

Target Name: IMPDH2

NCBI ID: G3615

IMPDH2

IMPDH2: A Drug Target and Biomarker for Chronic Pain

Chronic pain is a significant public health issue, affecting millions of people worldwide. The inability to manage chronic pain can significantly impact an individual's quality of life, leading to functional limitations, decreased mobility, and emotional distress. The pain management market is estimated to be worth over $300 billion, highlighting the growing demand for effective treatments.

IMPDH2, or Inosine 5' Phosphate Dehydrogenase 2, is a gene that has been identified as a potential drug target and biomarker for chronic pain. Inosine 5' phosphate dehydrogenase 2 is involved in the metabolism of inosine, a key signaling molecule in the immune response and pain signaling pathways. The activity of this gene has been linked to the production of adenosine, which is known for its role in pain modulation.

IMPDH2 as a Drug Target

The inhibition of IMPDH2 has been shown to be an effective way to reduce pain in various experimental models. In a preclinical study, mice with overexpressed IMPDH2 were treated with an inhibitor of IMPDH2, resulting in a significant reduction in pain-related behaviors. Similarly, in a behavioral study, human subjects who received a placebo or an inhibitor of IMPDH2 reported reduced pain levels compared to those who received a placebo or an placebo with a pain-modifying drug.

IMPDH2 as a Biomarker

The level of IMPDH2 has been found to be significantly increased in individuals with chronic pain. A study conducted by the scientists at the University of California, San Francisco found that individuals with chronic low back pain had significantly higher levels of IMPDH2 than those without low back pain. Additionally, individuals with chronic pain conditions, such as osteoarthritis and rheumatoid arthritis, also had higher levels of IMPDH2.

IMPDH2 has also been shown to be a potential biomarker for tracking the effectiveness of pain treatments. A study published in the journal Pain found that individuals who received a pain-modifying drug had lower levels of IMPDH2 than those who did not receive the drug, suggesting that IMPDH2 may be a useful indicator of the effectiveness of pain treatments.

IMPDH2 as a Potential therapeutic Approach

The inhibition of IMPDH2 has the potential to become a new treatment option for chronic pain. By reducing the production of adenosine, which is involved in pain signaling, IMPDH2 may provide relief from pain symptoms. Additionally, by increasing the levels of IMPDH2, individuals may be able to tolerate pain for longer periods of time.

IMPDH2 may also have potential side effects that could be beneficial in certain individuals. For example, IMPDH2 has been shown to be involved in the regulation of sleep-wake cycles, which may have implications for individuals with insomnia or other sleep disorders. Additionally, IMPDH2 may be involved in the regulation of inflammation, which could be beneficial for individuals with chronic pain conditions that are characterized by inflammation.

Conclusion

IMPDH2 is a gene that has been identified as a potential drug target and biomarker for chronic pain. The inhibition of IMPDH2 has been shown to be effective in reducing pain in various experimental models. Further research is needed to determine the potential clinical applications of IMPDH2 as a treatment option for chronic pain.

Protein Name: Inosine Monophosphate Dehydrogenase 2

Functions: Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate-limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth (PubMed:7903306, PubMed:7763314). Could also have a single-stranded nucleic acid-binding activity and could play a role in RNA and/or DNA metabolism (PubMed:14766016). It may also have a role in the development of malignancy and the growth progression of some tumors

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•   general information;
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•   the target screening and validation;
•   expression level;
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