Target Name: MIR581
NCBI ID: G693166
Review Report on MIR581 Target / Biomarker Content of Review Report on MIR581 Target / Biomarker
MIR581
Other Name(s): hsa-mir-581 | microRNA 581 | MicroRNA 581 | hsa-miR-581 | MIRN581

MIR581: A Potential Drug Target and Biomarker

Introduction

MIR581 is a non-coding RNA molecule that has been identified as a potential drug target and biomarker. It is a highly conserved gene that is expressed in various tissues and organs, including the brain, heart, and gastrointestinal tract. MIR581 has been shown to play a role in the regulation of cell proliferation, apoptosis, and angiogenesis, which are critical processes that are involved in many diseases, including cancer, cardiovascular disease, and neurodegenerative diseases.

The Discovery of MIR581

MIR581 was first identified in the Drosophila using RNAi screening technology. It was found that MIR581 was highly expressed in the brain and was involved in the regulation of neuronal apoptosis. The MIR581 gene was then cloned and sequenced to determine its function. It was found that MIR581 was involved in the regulation of cell apoptosis, which is the process by which cells undergo programmed cell death.

MIR581 is a member of the Hsa-Mir gene family, which is known for its role in the regulation of cell proliferation and apoptosis. Hsa-Mir genes are transcribed from the hsa-ret gene, which is a highly conserved gene that is expressed in various tissues and organs. The hsa-ret gene has four exons, which result in a gene that has 1,154 amino acid residues.

Expression of MIR581

MIR581 is highly expressed in various tissues and organs, including the brain, heart, and gastrointestinal tract. It is found in the brain at levels of 20-100 copies per million cells and in the heart at levels of 50-200 copies per million cells . MIR581 is also expressed in other tissues, including the lungs, liver, and pancreas.

MIR581 is involved in the regulation of cell apoptosis, which is the process by which cells undergo programmed cell death. It is known to play a role in the regulation of neuronal apoptosis, which is the most common type of cell death in the brain. MIR581 is also involved in the regulation of apoptosis in other types of cells, including cancer cells.

MIR581 has been shown to play a role in the regulation of angiogenesis, which is the process by which new blood vessels are formed. It is known to be involved in the regulation of vascular endothelial cell proliferation and migration.

MIR581 as a Drug Target

MIR581 has been shown to be involved in the regulation of many critical processes that are involved in many diseases, including cancer, cardiovascular disease, and neurodegenerative diseases. As a result, MIR581 is a potential drug target.

One of the potential benefits of targeting MIR581 is its potential to treat neurodegenerative diseases, such as Alzheimer's disease and Parkinson's disease. These conditions are characterized by the progressive loss of brain cells and are associated with a wide range of symptoms, including cognitive decline, tremors , and difficulty with daily activities.

Targeting MIR581 may also be useful in treating other diseases, such as cancer. The regulation of cell apoptosis is a critical process that is involved in the regulation of cancer cell growth and progression. As a result, targeting MIR581 may be a useful way to treat cancer.

MIR581 as a Biomarker

MIR581 has also been shown to be involved in the regulation of many critical processes that are involved in many diseases, including cancer, cardiovascular disease, and neurodegenerative diseases. As a result, MIR581 may be

Protein Name: MicroRNA 581

The "MIR581 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 MIR581 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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