Target Name: MIR633
NCBI ID: G693218
Review Report on MIR633 Target / Biomarker Content of Review Report on MIR633 Target / Biomarker
MIR633
Other Name(s): microRNA 633 | hsa-miR-633 | hsa-mir-633 | MIRN633 | MicroRNA 633

Understanding MiRNA 633: A Potential Drug Target Or Biomarker

MicroRNA 633 (miRNA 633) is a non-coding RNA molecule that plays a crucial role in various biological processes. It is a key regulator of gene expression and has been implicated in a wide range of diseases, including cancer, neurodegenerative diseases, and developmental disorders. Despite its importance, little is known about miRNA 633 and its potential as a drug target or biomarker.

The miRNA 633 molecule was first identified in the brush border regions (contigs) of the human genome in 2005 by the smRNA search algorithm. Since then, numerous studies have demonstrated that miRNA 633 is involved in various cellular processes, including cell growth, apoptosis, angiogenesis, and inflammation.

One of the most striking features of miRNA 633 is its ability to target specific mRNAs for degradation. This process is known as targeted decay and is a critical mechanism for regulating gene expression in the cell. MiRNA 633 has been shown to target the mRNAs of various cellular pathways, including the TGF-β pathway, the PI3K/Akt pathway, and the NF-kappa-B pathway.

The TGF-β pathway is a well-established target for miRNA 633. TGF-β is a transcription factor that regulates cell growth, differentiation, and survival. MiRNA 633 has been shown to negatively regulate TGF-β activity by binding to its target mRNAs and preventing their translation into protein. This process is known as TGF-β inhibition and has been shown to play a role in the regulation of various cellular processes, including cell growth, apoptosis, and autophagy.

The PI3K/Akt pathway is another target of miRNA 633. PI3K is a protein that regulates cell signaling and is involved in various cellular processes, including cell survival and angiogenesis. MiRNA 633 has been shown to target the mRNAs of the PI3K/ Akt pathway by binding to their coding regions, preventing their translation into protein, and leading to their degradation.

The NF-kappa-B pathway is also a target of miRNA 633. NF-kappa-B is a transcription factor that regulates inflammation and cellular signaling. MiRNA 633 has been shown to target the mRNAs of the NF-kappa-B pathway by binding to their coding regions, preventing their translation into protein, and leading to their degradation.

In addition to its effects on target mRNAs, miRNA 633 has also been shown to have a role in the regulation of miRNA itself. processes. This interaction between MiRNA 633 and MiRNA 21 suggests that MiRNA 633 may be a negative regulator of MiRNA 21 activity.

Despite its importance, the full potential of miRNA 633 as a drug target or biomarker remains to be explored. Several studies have demonstrated the potential of miRNA 633 as a drug target by showing that inhibiting its activity can lead to therapeutic effects in various models of disease , including cancer, neurodegenerative diseases, and developmental disorders.

In addition, miRNA 633 has also been shown to be a potential biomarker for several diseases. The miRNA 633 gene has been shown to be downregulated in various diseases, including cancer, neurodegenerative diseases, and developmental disorders [18] . This suggests that miRNA 633 may be a useful biomarker for these diseases and could be targeted by therapeutic approaches aimed at increasing its expression.

In conclusion, miRNA 633 is a non-coding RNA molecule that plays a crucial

Protein Name: MicroRNA 633

The "MIR633 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 MIR633 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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