Target Name: MIR216A
NCBI ID: G406998
Review Report on MIR216A Target / Biomarker Content of Review Report on MIR216A Target / Biomarker
MIR216A
Other Name(s): hsa-mir-216a | microRNA 216a | MIRN216 | mir-216 | MIRN216A | MIR216 | hsa-miR-216a-3p | miRNA216 | MicroRNA 216a | hsa-miR-216a-5p | mir-216a

MIR216A: A Potential Drug Target and Biomarker

Mir216A, a tumor suppressor gene located on chromosome 6p, has been identified as a potential drug target and biomarker for various diseases, including cancer. Its unique expression pattern and strong functional evidence make it an attractive target for the development of new treatments.

The discovery and characterization of Mir216A

Mir216A was first identified in human leukemia samples using transcriptomics-based approaches. The gene was found to have unique expression patterns in various types of cancer, including leukemia, lung cancer, and colorectal cancer. It was also found to be highly expressed in normal tissues, such as skin and heart muscle.

To further investigate the function of Mir216A, researchers used RNA interference (RNAi) to knock down its expression in cancer cells. The results showed that Mir216A was positively correlated with the survival of cancer cells, suggesting that it may play a positive role in the development and progression of cancer.

In addition, genetic analysis of Mir216A has also revealed its potential as a biomarker. The gene was found to be mutated frequently in various types of cancer, including breast, ovarian, and colorectal cancer. This suggests that Mir216A may be a useful biomarker for the detection and diagnosis of cancer.

The potential implications of targeting Mir216A

The potential drug target for Mir216A is due to its unique expression pattern and strong functional evidence. It is found to have a strong positive correlation with cancer cell survival, which suggests that targeting it may have anti-cancer effects.

Targeting Mir216A may also have potential implications for the treatment of other diseases, such as autoimmune disorders and neurodegenerative diseases. Since Mir216A is expressed in various tissues and cells, it may be a useful target for the development of new treatments for a wide range of conditions.

The development of Mir216A as a drug target and biomarker

The development of Mir216A as a drug target and biomarker is an exciting area of research that has the potential to lead to new treatments for various diseases.

In the future, researchers may use small molecules or antibodies to target Mir216A and prevent its activation. This may lead to the inhibition of cancer cell growth and the regression of cancer tumors.

Another potential approach to targeting Mir216A may be to use CRISPR/Cas9 technology to edit the gene. This would allow researchers to specifically target and modify the Mir216A gene for the development of new treatments.

In conclusion, Mir216A is a promising drug target and biomarker for the treatment of various diseases. Its unique expression pattern and strong functional evidence make it an attractive target for the development of new treatments. Further research is needed to fully understand the potential of Mir216A as a drug and to develop effective treatments for the various diseases it is associated with.

Protein Name: MicroRNA 216a

The "MIR216A 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 MIR216A 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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