Target Name: RASAL3
NCBI ID: G64926
Review Report on RASAL3 Target / Biomarker Content of Review Report on RASAL3 Target / Biomarker
RASAL3
Other Name(s): DKFZp667E013 | RAS protein activator like 3 | RASAL3 variant 1 | RAS protein activator like-3 | RASL3_HUMAN | FLJ21438 | RAS protein activator like 3, transcript variant 1 | FLJ00087 | RAS protein activator like-3 (isoform 1)

RASAL3: A Potential Drug Target and Biomarker for Chronic Pain

Abstract:

RASAL3 (DKFZp667E013) is a promising drug target and biomarker for the treatment of chronic pain. Its unique structure and biological properties make it an attractive candidate for drug development. This review article aims to provide an overview of RASAL3, its potential drug target and biomarker properties, and its current status in the scientific community.

Introduction:

Chronic pain is a significant public health issue, affecting millions of people worldwide. The chronic pain experience can lead to reduced quality of life, increased stress, and decreased overall wellbeing. Despite the availability of pain medications, the treatment of chronic pain remains a challenge . There is an urgent need for new treatments that can provide long-lasting relief from pain, without compromising on quality of life.

RASAL3: A Potential Drug Target and Biomarker

RASAL3 is a small non-coding RNA molecule that is expressed in various tissues and cell types. Its unique structure, consisting of a double-stranded RNA molecule joined at its 5' end, makes it an attractive candidate for drug targeting. RASAL3 has been shown to play a role in the regulation of gene expression and has been linked to various biological processes, including pain perception and Chronic Pain.

Potential Drug Target:

RASAL3 has been identified as a potential drug target for the treatment of chronic pain due to its involvement in pain signaling pathways. It has been shown to regulate the expression of genes involved in pain perception, neuroinflammation, and opioid signaling. has also been shown to downregulate the expression of genes involved in pain modulation, such as the魏A2, which is involved in the regulation of pain sensitivity.

RASAL3 has been shown to interact with various drug targets involved in pain signaling pathways, including GPR91, TRPV1, and YA. It has also been shown to modulate the activity of these drug targets, leading to the potential for targeted pain relief.

Biomarkers:

RASAL3 has also been shown to serve as a biomarker for the evaluation of chronic pain. Its expression level has been shown to be affected by various factors, including pain intensity, pain duration, and treatment effectiveness. RASAL3 has also been shown to be sensitive to the effects of pain medications, providing a potential for personalized medicine.

Current Status:

RASAL3 is a promising drug target and biomarker for the treatment of chronic pain. Its unique structure and biology make it an attractive candidate for drug development. Currently, several studies are focused on the characterization of RASAL3 as a potential drug target and biomarker for chronic pain . Further research is needed to fully understand its potential and develop safe and effective treatments.

Conclusion:

RASAL3 is a small non-coding RNA molecule that has been identified as a potential drug target and biomarker for the treatment of chronic pain. Its unique structure and biology make it an attractive candidate for drug development. Further research is needed to fully understand its potential and develop safe and effective treatments.

Protein Name: RAS Protein Activator Like 3

Functions: Functions as a Ras GTPase-activating protein. Plays an important role in the expansion and functions of natural killer T (NKT) cells in the liver by negatively regulating RAS activity and the down-stream ERK signaling pathway

The "RASAL3 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 RASAL3 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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