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Structural feature of TRAFs, their related human diseases and therapeutic intervention
Hyun Ho Park1,2
1College of Pharmacy, Chung-Ang University, Seoul, 06974, Republic of Korea. xrayleox@cau.ac.kr.
Abstract:
Several studies have been conducted over the years to unravel the structural information on the receptors that bind to tumor necrosis factor receptor-associated factor (TRAF) and the driving forces for the TRAF/receptor complex. In addition, studies have also been performed to highlight the influence of TRAF malfunctioning and mutations on the development of human disease. However, a holistic study that systematically summarizes the available information and the existing clinical trends towards development of the TRAF-targeting drugs has not been conducted to date. Herein, I reviewed existing research that focused on the structural information of various receptors recognized by the different members of the TRAF family. I also reviewed studies on the different human diseases that occur due to TRAF malfunctioning or mutations as well as the clinical trials undertaken to treat TRAF-associated diseases.
Insights
This review summarizes structural insights into tumor necrosis factor receptor-associated factor (TRAF) interactions and their role in human diseases. It highlights current clinical trends for developing TRAF-targeting drugs.
Area of Science:
- Molecular Biology
- Structural Biology
- Immunology
Background:
- Tumor necrosis factor receptor-associated factors (TRAFs) are crucial signaling adaptors.
- Dysfunctional TRAFs and mutations are implicated in various human diseases.
- Existing research lacks a comprehensive overview of TRAF-receptor interactions and therapeutic strategies.
Purpose of the Study:
- To systematically review structural information on TRAF-receptor complexes.
- To consolidate knowledge on TRAF-associated human diseases.
- To analyze clinical trends in the development of TRAF-targeting drugs.
Main Methods:
- Literature review of structural biology studies on TRAF-receptor interactions.
- Review of research on TRAF mutations and associated pathologies.
- Analysis of clinical trial data for TRAF-targeted therapies.
Main Results:
- Detailed structural insights into diverse TRAF-receptor binding interfaces.
- Identification of specific TRAF malfunctions and mutations linked to diseases like cancer and autoimmune disorders.
- Overview of ongoing and completed clinical trials for TRAF-based therapeutics.
Conclusions:
- A unified understanding of TRAF-receptor structures is essential for drug development.
- Targeting TRAFs offers a promising therapeutic avenue for various human diseases.
- Further research and clinical trials are needed to fully exploit TRAF-targeting strategies.
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