Target Name: MIR4784
NCBI ID: G100616378
Review Report on MIR4784 Target / Biomarker Content of Review Report on MIR4784 Target / Biomarker
MIR4784
Other Name(s): hsa-mir-4784 | hsa-miR-4784 | MicroRNA 4784 | microRNA 4784

MIR4784: A Potential Drug Target and Biomarker for Obesity and Insulin Resistance

Obesity and insulin resistance are two of the leading causes of metabolic diseases, such as type 2 diabetes, heart disease, and certain cancers. According to the World Health Organization (WHO), the number of adults classified as obese has more than tripled worldwide since the 1970s, and it is estimated that there will be over 7.5 billion people living in obesity by 2050. These conditions are caused by a combination of genetic and environmental factors, including an imbalance of calories, lack of physical activity, and an obesity-promoting diet.

One of the key drivers of obesity and insulin resistance is the inflammation that occurs in the body. Chronic inflammation can cause inflammation throughout the body, leading to a range of health problems, including obesity and type 2 diabetes.

MIR4784 is a protein that has been identified as a potential drug target and biomarker for obesity and insulin resistance. It is found in the obese and is associated with an increased risk of developing type 2 diabetes.

Research has shown that MIR4784 plays a key role in the development and progression of obesity. It is a key regulator of the inflammatory response and has been shown to contribute to the development of obesity by causing inflammation throughout the body.

One of the key functions of MIR4784 is its role in regulating the appetite. MIR4784 is a potent inhibitor of the appetite-sensitive hormone leptin, which means that it can help people lose weight by decreasing their food intake.

Another function of MIR4784 is its role in regulating inflammation. MIR4784 has been shown to reduce inflammation throughout the body, which can help to reduce the risk of chronic diseases such as obesity and type 2 diabetes.

In addition to its potential as a drug target, MIR4784 has also been identified as a potential biomarker for obesity and insulin resistance. Obesity is often associated with elevated levels of certain biomarkers, such as Insulin-like growth factor 1 (IGF-1), which is a key regulator of insulin sensitivity.

Research has shown that MIR4784 can also be used as a biomarker for insulin resistance. MIR4784 has been shown to reduce insulin sensitivity in obese individuals, which can help to increase the body's sensitivity to insulin and improve insulin sensitivity.

MIR4784 has also been shown to be involved in the regulation of energy metabolism. It has been shown to reduce energy intake in obese individuals, which can help to reduce the overall energy intake and lead to weight loss.

In conclusion, MIR4784 is a protein that has been identified as a potential drug target and biomarker for obesity and insulin resistance. Its functions include regulating appetite, inflammation, energy metabolism, and weight loss. Further research is needed to determine its potential as a drug and to develop biomarkers for obesity and insulin resistance.

Please note that this article is for general information purposes only and should not be taken as medical advice.

Protein Name: MicroRNA 4784

The "MIR4784 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 MIR4784 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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