Target Name: MIR887
NCBI ID: G100126347
Review Report on MIR887 Target / Biomarker Content of Review Report on MIR887 Target / Biomarker
Other Name(s): microRNA 887 | hsa-miR-887-3p | MIRN887 | hsa-mir-887 | MicroRNA 887 | hsa-miR-887-5p

MIR887: A Promising Drug Target and Biomarker

In recent years, scientific research has focused on identifying potential drug targets and biomarkers for various diseases. Among these, MIR887 has emerged as a promising molecule with great therapeutic potential. This article will discuss the significance of MIR887 as both a drug target and biomarker, shedding light on its unique properties and potential applications.

Understanding MIR887

MIR887, also known as microRNA-887, is a small noncoding RNA molecule that plays a vital role in various cellular processes. It is part of the microRNA family, which regulate gene expression by binding to messenger RNAs (mRNAs) and inhibiting their translation or promoting their degradation. MIR887 is encoded by a specific gene and can be found in several tissues and body fluids, including blood, saliva, and urine.

MIR887 as a Drug Target

One of the primary reasons for the interest in MIR887 as a drug target is its involvement in disease mechanisms. Studies have shown that dysregulation of MIR887 expression is associated with the progression of various diseases, including cancer, cardiovascular disorders, and autoimmune diseases.

In cancer, MIR887 has been shown to act as both a tumor suppressor and an oncogene, depending on the specific context. For instance, in breast cancer, MIR887 downregulates the expression of genes involved in tumor cell proliferation and migration, thus acting as a tumor suppressor. Conversely, in lung cancer, MIR887 promotes tumor cell survival and metastasis by inhibiting the expression of tumor suppressor genes.

Targeting MIR887 with specific drugs or therapies holds great potential for manipulating its expression levels and, consequently, exerting a therapeutic effect in disease treatment. By developing molecules that can either upregulate or downregulate MIR887, researchers can potentially inhibit its oncogenic effects or enhance its tumor suppressor activities. This targeted approach may lead to more personalized and effective treatment strategies for cancer patients.

Moreover, MIR887's involvement in other diseases, such as cardiovascular disorders and autoimmune diseases, further highlights its potential as a drug target. In these conditions, modulating MIR887 levels could potentially help regulate immune responses or restore normal cardiac functions, ultimately improving patient outcomes.

MIR887 as a Biomarker

Aside from its potential as a drug target, MIR887 has shown promise as a biomarker for various diseases. Biomarkers are measurable substances or indicators that can be used to evaluate or predict disease progression, response to therapy, or overall patient prognosis. MIR887's unique characteristics make it a valuable biomarker candidate across several medical fields.

For instance, in cancer diagnosis and prognosis, the expression levels of MIR887 have been found to correlate with tumor stage, metastasis, and patient survival rates. By measuring the levels of MIR887 in a patient's tissue or bodily fluids, healthcare professionals can gain insights into disease progression and tailor treatment strategies accordingly.

In cardiovascular diseases, MIR887 has been implicated in the regulation of endothelial cell functions, vascular remodeling, and atherosclerosis. Its expression patterns in blood samples have been associated with the severity of cardiovascular conditions, making it a potential biomarker for risk stratification and disease monitoring.

Furthermore, studies have also investigated the usefulness of MIR887 as a biomarker for autoimmune diseases, such as rheumatoid arthritis and multiple sclerosis. Dysregulated MIR887 expression has been observed in patients with these conditions, suggesting its potential as a disease-specific biomarker for early diagnosis and monitoring treatment effectiveness.

The Future of MIR887

As research on MIR887 advances, its therapeutic implications and diagnostic potential continue to unfold. The use of MIR887 as a drug target holds the promise of more precise and personalized therapies, while its value as a biomarker offers new opportunities for early disease detection and monitoring.

However, challenges remain in fully understanding the complex mechanisms underlying MIR887's actions and translating this knowledge into clinical applications. Further research is needed to elucidate the specific molecular targets of MIR887 in different disease contexts and develop effective methods to modulate its expression. Additionally, large-scale clinical trials are necessary to validate its role as a biomarker in diverse patient populations.

In conclusion, MIR887's unique properties as both a drug target and biomarker make it an exciting area of research in modern medicine. Its potential to influence disease progression and provide valuable diagnostic insights offers hope for improving patient outcomes in a wide range of diseases. As scientists continue to unravel the mysteries of MIR887, we may witness the development of innovative therapies and diagnostic tools that could revolutionize healthcare practices.

Protein Name: MicroRNA 887

The "MIR887 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 MIR887 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

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