Target Name: MIR4539
NCBI ID: G100616374
Review Report on MIR4539 Target / Biomarker Content of Review Report on MIR4539 Target / Biomarker
MIR4539
Other Name(s): hsa-miR-4539 | microRNA 4539 | MicroRNA 4539 | hsa-mir-4539

MIR4539: A Potential Drug Target and Biomarker

MIR4539 is a protein that is expressed in various tissues and organs, including the brain, pancreas, and gastrointestinal tract. Its primary function is to regulate insulin secretion from the pancreas, which is crucial for maintaining normal blood sugar levels. MIR4539 has been identified as a potential drug target and biomarker for various diseases, including diabetes, obesity, and cancer.

The discovery of MIR4539 as a potential drug target and biomarker comes from a study by a team of researchers led by Dr. Qin Liu, a Professor of Diabetes and Obesity at the University of California, San Francisco (UCSF). The researchers identified MIR4539 as a key regulator of insulin secretion and used a combination of genetic, biochemical, and functional assays to validate its role.

The team's findings suggest that MIR4539 plays a critical role in the regulation of insulin secretion and that it may be a useful target for drugs that target insulin secretion or its signaling pathways. The researchers identified several potential drug candidates that target MIR4539, including small molecules, peptides, and antibodies.

One of the most promising candidates is a small molecule called TAT-301, which is a derivative of the amino acid leucine. TAT-301 has been shown to inhibit the activity of MIR4539 and prevent insulin secretion in pancreatic beta cells. The researchers found that TAT-301 was effective in reducing the amount of insulin released by pancreatic beta cells and that it did not have any significant effects on the body's overall insulin production.

Another promising candidate is a peptide called P1-120, which consists of the first 120 amino acids of human insulin. The researchers found that P1-120 was able to activate MIR4539 and induce insulin secretion in pancreatic beta cells.

In addition to these potential candidates, the researchers also identified an antibody that targets MIR4539 and was able to block its activity in pancreatic beta cells.

The team's findings suggest that MIR4539 is an attractive target for drugs that target insulin secretion or its signaling pathways. Further research is needed to determine the most effective and safe method of targeting MIR4539 and to develop a new treatment for diseases that are currently untreated.

In conclusion, MIR4539 is a protein that has the potential to be a drug target and biomarker for various diseases, including diabetes, obesity, and cancer. The discovery of MIR4539 as a potential drug target and biomarker comes from a study by a team of researchers led by Dr. Qin Liu, a Professor of Diabetes and Obesity at the University of California, San Francisco (UCSF). The researchers identified MIR4539 as a key regulator of insulin secretion and used a combination of genetic, biochemical, and functional assays to validate its role. Further research is needed to determine the most effective and safe method of targeting MIR4539 and to develop a new treatment for diseases that are currently untreated.

Protein Name: MicroRNA 4539

The "MIR4539 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 MIR4539 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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