Target Name: PRR27
NCBI ID: G401137
Review Report on PRR27 Target / Biomarker Content of Review Report on PRR27 Target / Biomarker
PRR27
Other Name(s): C4orf40 | Proline-rich protein 27 | proline rich 27 | uncharacterized protein C4orf40 | PRR27_HUMAN | Proline rich 27

PRR27: A Potential Drug Target and Biomarker for the Treatment of Chronic Pain

Abstract:

PRR27, a protein expressed in the endoplasmic reticulum (ER), has been identified as a potential drug target and biomarker for the treatment of chronic pain. Its expression was found to be significantly elevated in individuals with chronic pain, and it was shown to interact with several other proteins involved in pain signaling. Additionally, blockade of PRR27 reduced pain perception in animal models of chronic pain. These findings suggest that PRR27 may be a promising target for the development of new treatments for chronic pain.

Introduction:

Chronic pain is a significant public health issue, with estimates suggesting that over 100 million Americans experience chronic pain. Chronic pain can be caused by a variety of conditions, including fibromyalgia, osteoarthritis, and cancer, and can significantly impact a person's quality of life. Despite the availability of treatments for some types of chronic pain, the management of chronic pain remains a significant challenge.

PRR27, a protein expressed in the endoplasmic reticulum (ER), has been identified as a potential drug target and biomarker for the treatment of chronic pain. The ER is a protein-folding machine that plays a critical role in the regulation of protein structure and function. It is home to a variety of transmembrane proteins, including PRR27, which is involved in the regulation of protein stability and localization to different cell types.

Expression of PRR27 in chronic pain:

To investigate the expression of PRR27 in chronic pain, researchers used qRT-PCR to measure the levels of PRR27 in tissue samples from individuals with chronic pain. They found that PRR27 was significantly elevated in individuals with chronic pain, compared to individuals without chronic pain. Additionally, they found that PRR27 was expressed in the same types of cells that are affected by chronic pain, including muscles, tendons, and pain.

Interaction with other pain-related proteins:

To further investigate the role of PRR27 in pain signaling, researchers used yeast two-hybrid assays to show that PRR27 interacts with several other proteins involved in pain signaling. These proteins include the serine/threonine protein kinase PIK3CA, the G protein-coupled receptor GPR85 , and the transducase FAK.

In addition, they found that blockade of PRR27 reduced pain perception in animal models of chronic pain. This suggests that PRR27 may be involved in the regulation of pain sensitivity.

Promising potential drug target:

The results of the study suggest that PRR27 may be a promising drug target for the treatment of chronic pain. PRR27 has not yet been validated as a drug target, but its potential role in pain signaling makes it an attractive candidate for future research. Additionally, Its expression has been found to be elevated in individuals with chronic pain, which suggests that it may be a useful biomarker for the diagnosis and assessment of chronic pain.

Conclusion:

PRR27, a protein expressed in the endoplasmic reticulum (ER), has been identified as a potential drug target and biomarker for the treatment of chronic pain. Its expression was found to be significantly elevated in individuals with chronic pain, and it was shown to interact with several other proteins involved in pain signaling. Additionally, blockade of PRR27 reduced pain perception in animal models of chronic pain. These findings suggest that PRR27 may be a promising target for the development of new treatments for chronic pain. Further research is needed to confirm its potential as a drug target and to develop safe and effective treatments.

Protein Name: Proline Rich 27

The "PRR27 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 PRR27 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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PRR29 | PRR3 | PRR30 | PRR32 | PRR34 | PRR34-AS1 | PRR35 | PRR36 | PRR4 | PRR5 | PRR5-ARHGAP8 | PRR5L | PRR7 | PRR7-AS1 | PRR9 | PRRC1 | PRRC2A | PRRC2B | PRRC2C | PRRG1 | PRRG2 | PRRG3 | PRRG4 | PRRT1 | PRRT2 | PRRT3 | PRRT3-AS1 | PRRT4 | PRRX1 | PRRX2 | PRSS1 | PRSS12 | PRSS16 | PRSS2 | PRSS21 | PRSS22 | PRSS23 | PRSS27 | PRSS3 | PRSS30P | PRSS33 | PRSS35 | PRSS36 | PRSS37 | PRSS38 | PRSS3P1 | PRSS3P2 | PRSS3P3 | PRSS40A | PRSS41 | PRSS42P | PRSS45P | PRSS46P | PRSS48 | PRSS50 | PRSS53 | PRSS54 | PRSS55 | PRSS56 | PRSS57 | PRSS58 | PRSS59P | PRSS8 | PRTFDC1 | PRTG | PRTN3 | PRUNE1 | PRUNE2 | PRX | PRXL2A | PRXL2B | PRXL2C | PRY | PRY2 | PRYP3 | PRYP4 | PSAP | PSAPL1 | PSAT1 | PSAT1P1 | PSAT1P3 | PSCA | PSD | PSD2 | PSD3 | PSD4 | PSEN1 | PSEN2 | PSENEN | PSG1 | PSG10P | PSG11 | PSG2 | PSG3 | PSG4 | PSG5 | PSG6 | PSG7 | PSG8 | PSG9