Target Name: RFWD3
NCBI ID: G55159
Review Report on RFWD3 Target / Biomarker Content of Review Report on RFWD3 Target / Biomarker
RFWD3
Other Name(s): RING-type E3 ubiquitin transferase RFWD3 | RNF201 | E3 ubiquitin-protein ligase RFWD3 | RFWD3_HUMAN | RING finger and WD repeat domain-containing protein 3 | Ring finger and WD repeat domain 3 | RFWD3 variant 1 | RING finger protein 201 | FANCW | ring finger and WD repeat domain 3 | Ring finger and WD repeat domain 3, transcript variant 1 | E3 ubiquitin-protein ligase RFWD3 (isoform 1)

Targeting RFWD3: Potential Therapeutic Approaches for Diseases

Ring-type E3 ubiquitin transferase (RFWD3) is a key enzyme in the ubiquitin system, which is a protein degradation pathway that is essential for cell signaling, tissue repair, and homeostasis. Mutations in the RFWD3 gene have been linked to a variety of diseases, including cancer, neurodegenerative diseases, and autoimmune disorders. As a result, targeting RFWD3 has become an attractive research focus in recent years.

Diseases associated with RFWD3 mutations

RFWD3 mutations have been implicated in the development and progression of several diseases, including cancer, neurodegenerative diseases, and autoimmune disorders.

1. Cancer

RFWD3 mutations have been found to be associated with the development of various types of cancer, including breast, ovarian, and colorectal cancers. In breast cancer, RFWD3 mutations have been found to be associated with poor prognosis and increased resistance to chemotherapy. In colorectal cancer, RFWD3 mutations have been found to be associated with tumor progression and reduced response to chemotherapy.

2. Neurodegenerative diseases

RFWD3 mutations have been implicated in the development and progression of neurodegenerative diseases, including Alzheimer's disease, Parkinson's disease, and Huntington's disease. In these diseases, RFWD3 mutations have been found to contribute to the build-up of toxic protein aggregates and the progressive loss of brain cells.

3. Autoimmune disorders

RFWD3 mutations have also been implicated in the development and progression of autoimmune disorders, including rheumatoid arthritis, lupus, and multiple sclerosis. In these diseases, RFWD3 mutations have been found to contribute to the development of autoimmune responses and the production of autoantibodies.

RFWD3 as a drug target

The potential therapeutic targets for RFWD3 mutations are vast and include a range of potential drug targets, including inhibitors of the activity of RFWD3, modulators of its expression, and modulators of its downstream targets.

1. Inhibitors of RFWD3 activity

One potential therapeutic approach to targeting RFWD3 mutations is the development of inhibitors of its activity. These inhibitors could be used to treat a variety of diseases associated with RFWD3 mutations, including cancer, neurodegenerative diseases, and autoimmune disorders.

2. Modulators of RFWD3 expression

Another potential therapeutic approach to targeting RFWD3 mutations is the development of modulators of its expression. These modulators could be used to increase the amount of RFWD3 protein produced or to alter its localization in the cell.

3. Modulators of RFWD3 downstream targets

A third potential therapeutic approach to targeting RFWD3 mutations is the development of modulators of its downstream targets. These modulators could be used to regulate the activity of RFWD3 and its downstream targets, including factors that influence cell signaling pathways.

Conclusion

RFWD3 is a key enzyme in the ubiquitin system that has been implicated in the development and progression of a variety of diseases. As a result, targeting RFWD3 has become an attractive research focus in recent years. The development of inhibitors of RFWD3 activity, modulators of RFWD3 expression, and modulators of RFWD3 downstream targets may hold promise as potential therapeutic approaches for treating RFWD3-related diseases. Further research is needed to fully understand the role of RFWD3 in disease and to develop effective treatments.

Protein Name: Ring Finger And WD Repeat Domain 3

Functions: E3 ubiquitin-protein ligase required for the repair of DNA interstrand cross-links (ICL) in response to DNA damage (PubMed:21504906, PubMed:21558276, PubMed:26474068, PubMed:28575657, PubMed:28575658). Plays a key role in RPA-mediated DNA damage signaling and repair (PubMed:21504906, PubMed:21558276, PubMed:26474068, PubMed:28575657, PubMed:28575658, PubMed:28691929). Acts by mediating ubiquitination of the RPA complex (RPA1, RPA2 and RPA3 subunits) and RAD51 at stalled replication forks, leading to remove them from DNA damage sites and promote homologous recombination (PubMed:26474068, PubMed:28575657, PubMed:28575658). Also mediates the ubiquitination of p53/TP53 in the late response to DNA damage, and acts as a positive regulator of p53/TP53 stability, thereby regulating the G1/S DNA damage checkpoint (PubMed:20173098). May act by catalyzing the formation of short polyubiquitin chains on p53/TP53 that are not targeted to the proteasome (PubMed:20173098). In response to ionizing radiation, interacts with MDM2 and enhances p53/TP53 ubiquitination, possibly by restricting MDM2 from extending polyubiquitin chains on ubiquitinated p53/TP53 (PubMed:20173098)

The "RFWD3 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 RFWD3 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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