Target Name: ARID5B
NCBI ID: G84159
Review Report on ARID5B Target / Biomarker Content of Review Report on ARID5B Target / Biomarker
ARID5B
Other Name(s): MRF1-like protein | Modulator recognition factor 2 | AT-rich interaction domain 5B, transcript variant 2 | ARID domain-containing protein 5B | Modulator recognition factor 2 (MRF2) | AT-rich interactive domain 5B (MRF1-like) | RP11-341A19.1 | AT-rich interaction domain 5B | AT-rich interactive domain-containing protein 5B | FLJ21150 | ARID5B variant 1 | DESRT | ARI5B_HUMAN | AT-rich interactive domain-containing protein 5B (isoform 1) | ARID5B variant 2 | AT-rich interactive domain-containing protein 5B (isoform 2) | modulator recognition factor 2 (MRF2) | MRF2 | MRF-2 | AT-rich interaction domain 5B, transcript variant 1

Understanding ARID5B: Potential Drug Target and Biomarker

ARID5B (Arsenical-Inducible Regulatory Interaction DNA-Binding Protein 5B) is a protein that has been identified as a potential drug target and biomarker for various diseases, including cancer, neurodegenerative diseases, and autoimmune disorders. Its unique mechanism of action and subcellular localization make it an attractive target for small molecules and other therapeutic agents. In this article, we will provide an overview of ARID5B, its potential drug targets, and its potential as a biomarker.

Potential Drug Targets

ARID5B is a member of the ARID domain family, which is known for its ability to regulate gene expression and DNA binding. This domain family also includes proteins that are involved in DNA repair, DNA replication, and DNA-protein interactions, suggesting that ARID5B may have a wide range of potential drug targets.

One of the most promising potential drug targets for ARID5B is the protein p53, which is a well-known tumor suppressor protein that plays a critical role in regulating cell growth, apoptosis, and DNA damage repair. p53 has been shown to interact with various proteins , including ARID5B, and studies have suggested that ARID5B may be a negative regulator of p53 function. This interaction between ARID5B and p53 suggests that targeting ARID5B may be a way to inhibit the activity of p53 and potentially lead to the development of cancer.

Another potential drug target for ARID5B is the protein heat shock protein (Hsp90), which is involved in protein-protein and protein-DNA interactions and has been shown to play a role in various cellular processes, including stress response, DNA replication, and repair , among others. Hsp90 has been shown to interact with ARID5B and studies have suggested that ARID5B may be a positive regulator of Hsp90 function. This interaction between ARID5B and Hsp90 suggests that targeting ARID5B may be a way to activate the activity of Hsp90 and potentially lead to the development of neurodegenerative diseases.

Biomarkers

ARID5B has also been identified as a potential biomarker for various diseases, including cancer, neurodegenerative diseases, and autoimmune disorders. Its unique subcellular localization and the ability to interact with various proteins make it an attractive target for diagnostic tools.

One of the most promising applications of ARID5B as a biomarker is its potential to serve as a diagnostic marker for cancer. ARID5B has been shown to be expressed in various types of cancer, including breast, ovarian, and prostate cancer. This suggests that it may be a useful biomarker for these diseases and could potentially be used in combination with other diagnostic tests to improve the accuracy of cancer diagnosis.

Another potential application of ARID5B as a biomarker is its ability to interact with various proteins, including the protein PD-L1. PD-L1 is a protein that has been shown to play a role in immune regulation and has been implicated in various autoimmune diseases. ARID5B has been shown to interact with PD-L1 and studies have suggested that ARID5B may be a potential therapeutic target for autoimmune diseases.

Conclusion

In conclusion, ARID5B is a protein that has been identified as a potential drug target and biomarker for various diseases. Its unique mechanism of action and subcellular localization make it an attractive target for small molecules and other therapeutic agents. The potential drug targets for ARID5B, including p53 and Hsp90, suggest that targeting ARID5B may be a way to inhibit the activity of these proteins and potentially lead to the development of cancer and neurodegenerative diseases. The potential use of ARID5B as a biomarker for cancer and autoimmune diseases makes it an attractive target for diagnostic tools and therapeutic agents. Further research is needed to fully understand the potential of ARID5B as a drug target and biomarker.

Protein Name: AT-rich Interaction Domain 5B

Functions: Transcription coactivator that binds to the 5'-AATA[CT]-3' core sequence and plays a key role in adipogenesis and liver development. Acts by forming a complex with phosphorylated PHF2, which mediates demethylation at Lys-336, leading to target the PHF2-ARID5B complex to target promoters, where PHF2 mediates demethylation of dimethylated 'Lys-9' of histone H3 (H3K9me2), followed by transcription activation of target genes. The PHF2-ARID5B complex acts as a coactivator of HNF4A in liver. Required for adipogenesis: regulates triglyceride metabolism in adipocytes by regulating expression of adipogenic genes. Overexpression leads to induction of smooth muscle marker genes, suggesting that it may also act as a regulator of smooth muscle cell differentiation and proliferation. Represses the cytomegalovirus enhancer

The "ARID5B 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 ARID5B 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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