Target Name: MIR216B
NCBI ID: G100126319
Review Report on MIR216B Target / Biomarker Content of Review Report on MIR216B Target / Biomarker
Other Name(s): MicroRNA 216b | MIRN216B | microRNA 216b | mir-216b | hsa-mir-216b | hsa-miR-216b-5p | hsa-miR-216b-3p

MIR216B: A Promising Drug Target and Biomarker in Disease

The discovery of microRNAs (miRNAs) has revolutionized our understanding of gene regulation and their role in various biological processes. These small non-coding RNA molecules have emerged as important regulators of gene expression, playing a crucial role in numerous diseases, including cancer, cardiovascular diseases, and neurological disorders. MIR216B, a specific miRNA, has gained significant attention in recent years as a potential drug target and biomarker for various diseases. In this article, we will explore the role of MIR216B and its potential implications in disease progression and treatment.

Understanding MIR216B

MIR216B is a member of the miR-216 family, which is located on chromosome 2 in humans. It is transcribed from the host gene "SLC12A5," which encodes a protein involved in ion transport across cellular membranes. MIR216B is primarily expressed in various tissues, including the brain, liver, heart, and kidney, suggesting its potential involvement in multiple physiological processes and disease pathways.

MIR216B as a Drug Target

As a miRNA, MIR216B acts as a natural post-transcriptional regulator of gene expression. It functions by binding to the 3' untranslated region (UTR) of target messenger RNAs (mRNAs), leading to their degradation or translational repression. MIR216B has been implicated in the regulation of several pathways involved in disease progression, making it an attractive target for therapeutic intervention.

One of the notable roles of MIR216B is its involvement in cancer. Studies have shown that MIR216B expression is often dysregulated in various types of cancer, including breast, lung, and colorectal cancer. It has been observed to act as a tumor suppressor, inhibiting tumor growth, metastasis, and angiogenesis through its target genes. Additionally, MIR216B has been associated with chemotherapeutic resistance, suggesting its potential as a target to overcome drug resistance.

Furthermore, MIR216B has been implicated in cardiovascular diseases, such as atherosclerosis and cardiac hypertrophy. It has been shown to regulate key genes involved in endothelial dysfunction, inflammation, and apoptosis, all of which contribute to disease progression. Targeting MIR216B may provide a novel approach to modulate these pathological processes and minimize cardiovascular complications.

MIR216B as a Biomarker

In addition to its potential as a therapeutic target, MIR216B holds promise as a biomarker for disease prognosis and diagnosis. Studies have consistently demonstrated altered expression levels of MIR216B in various diseases compared to healthy individuals, making it a potential candidate for disease detection and prognosis.

In cancer, aberrant expression of MIR216B has been associated with tumor stage, lymph node metastasis, and overall survival. Its expression levels have been analyzed in tumor tissues, blood samples, and even in exosomes, showing its potential use in liquid biopsies for cancer diagnosis and monitoring disease progression.

Similarly, in cardiovascular diseases, altered levels of MIR216B have been observed in patient samples. Its expression has been correlated with the severity of atherosclerosis and myocardial damage, providing valuable insights into disease progression and potential prognostic applications.

Challenges and Future Directions

While the potential of MIR216B as a drug target and biomarker is promising, several challenges remain. First, understanding the complexity of miRNA-mediated regulation and accurately identifying target genes of MIR216B are crucial for effective therapeutic intervention. Improvements in high-throughput sequencing technologies and bioinformatics analysis will aid in unraveling the intricate gene regulatory networks.

Second, the development of safe and effective delivery systems for miRNA-based therapies is essential. Efficient delivery vehicles and targeted delivery strategies need to be optimized to ensure specific and controlled delivery of MIR216B mimics or inhibitors to the desired tissues or cells.

Furthermore, large-scale clinical studies are required to validate the diagnostic and prognostic potential of MIR216B in various diseases. Establishing standardized protocols for sample collection, storage, and analysis will aid in comparing and combining data from different research groups.


MIR216B has emerged as a promising drug target and biomarker in various diseases. Its involvement in key disease pathways, including cancer and cardiovascular diseases, highlights its potential as a therapeutic target to halt disease progression. Moreover, its altered expression levels in patient samples make it a potential biomarker for disease diagnosis and prognosis. While challenges exist in harnessing the full potential of MIR216B, continued research and advancements in technology hold great promise for utilizing this miRNA in personalized medicine and improving patient outcomes.

Protein Name: MicroRNA 216b

The "MIR216B 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 MIR216B 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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