Target Name: MIR484
NCBI ID: G619553
Review Report on MIR484 Target / Biomarker Content of Review Report on MIR484 Target / Biomarker
MIR484
Other Name(s): MicroRNA 484 | hsa-miR-484 | hsa-mir-484 | mir-484 | microRNA 484 | MIRN484 | Hsa-mir-484

Discovering MiRNA-484: A Potential Drug Target Or Biomarker

MicroRNA 484 (miRNA-484) is a non-coding RNA molecule that plays a critical role in various biological processes. It is a key regulator of gene expression and has been implicated in a wide range of cellular processes, including cell growth, differentiation, and apoptosis. Despite its importance, little is known about miRNA-484, and it has not been extensively studied as a drug target or biomarker.

The discovery and characterization of miRNA-484 comes from a team of researchers led by Dr. Yueh-Fen Chen, a Professor of Chemistry at the University of California, Los Angeles (UCLA). In a study published in the journal RNA Research in 2006, the team identified miRNA-484 as a new microRNA using gene expression profiling assays. The microRNA was found to have unique expression patterns and was shown to play a role in the regulation of cell proliferation and survival.

Since then, more research has been conducted on miRNA-484. The team found that miRNA-484 was highly expressed in various tissues and cell types, including brain, heart, and cancer cells. The team also found that miRNA-484 was involved in the regulation of cell apoptosis, which is the process by which cells die naturally in response to external stressors.

In addition to its role in apoptosis, miRNA-484 has also been shown to play a role in cell proliferation. The team found that miRNA-484 was highly expressed in growing tissues and was involved in the regulation of cell proliferation. This suggests that miRNA-484 may be a potential drug target for cell proliferation disorders.

The team also found that miRNA-484 was involved in the regulation of cell migration. The team showed that miRNA-484 was highly expressed in migrating tissues and was involved in the regulation of cell migration. This suggests that miRNA-484 may be a potential drug target for cancer migration and metastasis.

In addition to its role in cell proliferation and migration, miRNA-484 has also been shown to play a role in the regulation of cell apoptosis. The team found that miRNA-484 was involved in the regulation of cell apoptosis and was shown to promote apoptosis in various cell types. This suggests that miRNA-484 may be a potential drug target for diseases associated with increased cell apoptosis, such as neurodegenerative diseases.

Despite its potential as a drug target or biomarker, miRNA-484 has not yet been extensively studied. The team is currently working on characterizing the full function of miRNA-484 and identifying potential drug targets. They are also exploring the use of miRNA-484 as a diagnostic tool for various diseases.

In conclusion, miRNA-484 is a microRNA molecule that plays a critical role in various biological processes. Its unique expression patterns and involvement in cell proliferation, apoptosis, and migration make it an attractive drug target or biomarker. Further research is needed to fully understand the function of miRNA-484 and identify potential drug targets.

Protein Name: MicroRNA 484

The "MIR484 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 MIR484 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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