Target Name: MIR3185
NCBI ID: G100422978
Review Report on MIR3185 Target / Biomarker Content of Review Report on MIR3185 Target / Biomarker
MIR3185
Other Name(s): hsa-miR-3185 | hsa-mir-3185 | MicroRNA 3185 | microRNA 3185

MIR3185: A Versatile Biomarker and Promising Drug Target

In recent years, researchers have made significant advancements in understanding the importance of non-coding RNAs, particularly microRNAs (miRNAs), in various cellular processes. One such miRNA, MIR3185, has gained attention as a versatile biomarker and an intriguing drug target. This article delves into the potential of MIR3185 in disease detection and treatment and explores its implications in targeted therapies.

The Role of MIR3185

MIR3185 belongs to the class of small non-coding RNAs known as miRNAs. These molecules exert their function by binding to messenger RNAs (mRNAs), leading to their degradation or translational repression. MIR3185, like other miRNAs, is involved in the post-transcriptional regulation of gene expression. While the precise molecular mechanisms of MIR3185's functions are yet to be fully elucidated, studies have suggested its involvement in several diseases and physiological processes.

MIR3185 as a Biomarker

In recent years, the identification of miRNAs as potential biomarkers for disease diagnosis and prognosis has opened up new avenues in precision medicine. MIR3185, too, has shown promising potential as a biomarker for various diseases, including cancer, cardiovascular disorders, and neurological conditions.

In cancer, aberrant expression of MIR3185 has been observed in multiple tumor types. Studies have shown that MIR3185 levels can distinguish between cancer patients and healthy individuals with remarkable accuracy. Moreover, its differential expression has been linked to tumor aggressiveness, patient survival rates, and response to treatment. This makes MIR3185 a valuable prognostic and predictive biomarker for personalized cancer management.

Interestingly, MIR3185 has also been associated with cardiovascular diseases, such as coronary artery disease and heart failure. Its altered expression patterns in both cardiac tissue and circulating miRNA profiles indicate potential as a diagnostic biomarker for cardiovascular conditions. Furthermore, evidence suggests that MIR3185 may regulate genes involved in inflammation, apoptosis, and endothelial function, which are critical processes in cardiovascular pathology.

In neurodegenerative disorders, MIR3185 has been implicated in the regulation of genes associated with neuronal survival, synaptic plasticity, and immune response. Its aberrant expression in the brain and cerebrospinal fluid of patients with Alzheimer's disease, Parkinson's disease, and multiple sclerosis suggests its potential for early detection and disease monitoring. The ability to measure MIR3185 levels non-invasively in biological fluids further enhances its utility as a biomarker in neurodegenerative diseases.

The identification of MIR3185 as a biomarker has significant clinical implications. Its detection in patient samples, either through the extraction of exosomal miRNAs or via circulating miRNA profiles, can potentially aid in early disease detection, monitoring treatment response, and guiding therapeutic interventions.

MIR3185 as a Therapeutic Target

The discovery of miRNAs as crucial regulators of gene expression has attracted considerable attention towards targeting these molecules for therapeutic purposes. MIR3185, with its involvement in various diseases, holds immense potential as a novel therapeutic target.

In cancer therapeutics, modulating MIR3185 expression offers a promising opportunity. Studies utilizing antisense oligonucleotides or synthetic miRNA mimics have shown the potential to restore or inhibit MIR3185 expression, thereby influencing cancer cell growth, migration, and invasion. Combination therapies involving MIR3185 manipulation, alongside conventional chemotherapy or targeted therapy, could enhance treatment efficacy and overcome drug resistance in certain tumor types.

The cardiovascular field could also benefit from targeting MIR3185. The precise regulation of MIR3185 levels may help mitigate pathological processes such as inflammation, oxidative stress, and endothelial dysfunction, which are underlying factors associated with atherosclerosis and heart failure. Utilizing synthetic modulators or gene editing techniques to control MIR3185 could potentially offer a novel therapeutic approach for cardiovascular diseases.

Moreover, neurodegenerative disorders may particularly benefit from targeting MIR3185. By manipulating MIR3185 expression in animal models, researchers have been able to modulate disease-associated phenotypes, neuronal survival, and neuroinflammation. This suggests that targeting MIR3185 may have therapeutic potential in slowing the progression of neurodegenerative diseases and preserving neuronal function.

The Path Forward

MIR3185, as a versatile biomarker and a potential therapeutic target, holds promise in revolutionizing disease management. The ability to detect and target this small non-coding RNA may improve diagnosis, guide treatment decisions, and introduce novel therapeutic strategies in several disease areas. Further research is necessary to fully understand the underlying mechanisms of MIR3185 and optimize its clinical translation. Nonetheless, the growing body of evidence supports the notion that MIR3185 has the potential to become a transformative tool in personalized medicine.

Protein Name: MicroRNA 3185

The "MIR3185 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 MIR3185 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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