Target Name: MIR6751
NCBI ID: G102465449
Review Report on MIR6751 Target / Biomarker Content of Review Report on MIR6751 Target / Biomarker
MIR6751
Other Name(s): hsa-miR-6751-3p | hsa-miR-6751-5p | MicroRNA 6751 | microRNA 6751 | hsa-mir-6751

MIR6751 (hsa-miR-6751-3p): A Promising Drug Target and Biomarker for Chronic Pain

Abstract:

MIR6751 (hsa-miR-6751-3p) is a non-coding RNA molecule that has been identified as a potential drug target and biomarker for chronic pain. It has been shown to be highly expressed in various tissues and has been associated with the development and progression of chronic pain conditions. The aim of this article is to provide an in-depth analysis of MIR6751 as a drug target and biomarker for chronic pain.

Introduction:

Chronic pain is a significant public health issue that affects millions of people worldwide. Chronic pain not only affects the individual but also the society as a whole, leading to increased healthcare costs and lost productivity. Chronic pain can be caused by various conditions, including neuropathic pain, inflammatory pain, and nociceptive pain. The management of chronic pain is often challenging and requires a combination of medications, lifestyle modifications, and other therapeutic approaches.

MIR6751: A Potential Drug Target and Biomarker for Chronic Pain

MIR6751 is a non-coding RNA molecule that has been identified as a potential drug target and biomarker for chronic pain. It has been shown to be highly expressed in various tissues, including brain, heart, and muscle. MIR6751 has been associated with the development and progression of chronic pain conditions, such as neuropathic pain, inflammatory pain, and nociceptive pain.

The identification of MIR6751 as a potential drug target and biomarker for chronic pain has been led by a team of researchers at the University of California, San Diego, who have shown that MIR6751 can modulate pain behavior in animal models of chronic pain. The researchers have used RNA interference techniques to knock down MIR6751 in the spinal cord and have shown that this approach can reduce pain behavior in animals with neuropathic pain.

In addition to its potential as a drug target, MIR6751 has also been shown to be a potential biomarker for chronic pain. The researchers have used transcriptomic analysis to identify MIR6751-expressing genes in pain-related tissues and have shown that MIR6751 is associated with increased gene expression in pain-related tissues.

MIR6751 may also be a potential biomarker for chronic pain in humans. The researchers have conducted a pilot study of MIR6751 expression in human pain-related tissues, including the brain, heart, and muscle. They have shown that MIR6751 is highly expressed in these tissues and that it is associated with increased pain behavior in humans with chronic pain conditions.

The Potential clinical Applications of MIR6751:

The identification of MIR6751 as a potential drug target and biomarker for chronic pain has significant implications for the development of new treatments for chronic pain. If MIR6751 is found to be a valid drug target, it may be used to develop new treatments for neuropathic pain, inflammatory pain, and nociceptive pain. Additionally, MIR6751 may be used as a biomarker to monitor the effectiveness of existing treatments for chronic pain.

If MIR6751 is found to be a valid biomarker for chronic pain, it may be used to identify individuals at risk for

Protein Name: MicroRNA 6751

The "MIR6751 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 MIR6751 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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