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DCUN1D1 and neddylation: Potential targets for cancer therapy
Juliano D Paccez1, Chiara L M Foret2, Jaira F de Vasconcellos3
1International Centre for Genetic Engineering and Biotechnology (ICGEB), Cape Town 7925, South Africa.
Abstract:
Cancer affects millions of people and understanding the molecular mechanisms related to disease development and progression is essential to manage the disease. Post-translational modification (PTM) processes such as ubiquitination and neddylation have a significant role in cancer development and progression by regulating protein stability, function, and interaction with other biomolecules. Both ubiquitination and neddylation are analogous processes that involves a series of enzymatic steps leading to the covalent attachment of ubiquitin or NEDD8 to target proteins. Neddylation modifies the CRL family of E3 ligase and regulates target proteins' function and stability. The DCUN1D1 protein is a regulator of protein neddylation and ubiquitination and acts promoting the neddylation of the cullin family components of E3-CRL complexes and is known to be upregulated in several types of cancers. In this review we compare the PTM ubiquitination and neddylation. Our discussion is focused on the neddylation process and the role of DCUN1D1 protein in cancer development. Furthermore, we provide describe DCUN1D1 protein and discuss its role in pathogenesis and signalling pathway in six different types of cancer. Additionally, we explore both the neddylation and DCUN1D1 pathways as potential druggable targets for therapeutic interventions. We focus our analysis on the development of compounds that target specifically neddylation or DCUN1D1. Finally, we provide a critical analysis about the challenges and perspectives in the field of DCUN1D1 and neddylation in cancer research. KEY POINTS: Neddylation is a post-translational modification that regulates target proteins' function and stability. One regulator of the neddylation process is a protein named DCUN1D1 and it is known to have its expression deregulated in several types of cancers. Here, we provide a detailed description of DCUN1D1 structure and its consequence for the development of cancer. We discuss both the neddylation and DCUN1D1 pathways as potential druggable targets for therapeutic interventions and provide a critical analysis about the challenges and perspectives in the field of DCUN1D1 and neddylation in cancer research.
Insights
Neddylation, a key protein modification, and its regulator DCUN1D1 are crucial in cancer. Targeting these pathways offers potential new cancer therapies, despite existing challenges.
Area of Science:
- Molecular Biology
- Biochemistry
- Oncology
Background:
- Post-translational modifications (PTMs) like ubiquitination and neddylation are vital in regulating protein function and stability, influencing cancer development.
- Neddylation specifically targets the CRL family of E3 ligases, impacting protein homeostasis.
- DCUN1D1, a regulator of neddylation, is frequently overexpressed in various cancers, highlighting its oncogenic role.
Purpose of the Study:
- To compare ubiquitination and neddylation as PTMs.
- To elucidate the role of the DCUN1D1 protein in cancer pathogenesis and signaling pathways.
- To explore the therapeutic potential of targeting neddylation and DCUN1D1 pathways in cancer treatment.
Main Methods:
- Comparative analysis of ubiquitination and neddylation processes.
- Detailed description of DCUN1D1 protein structure and function.
- Review of DCUN1D1's role in the pathogenesis of six distinct cancer types.
- Exploration of potential therapeutic strategies targeting neddylation and DCUN1D1.
Main Results:
- Neddylation and DCUN1D1 play significant roles in cancer development and progression.
- DCUN1D1's dysregulation contributes to oncogenesis.
- Both neddylation and DCUN1D1 pathways represent promising druggable targets for cancer therapy.
Conclusions:
- Targeting neddylation and DCUN1D1 offers a novel therapeutic avenue for cancer treatment.
- Further research is needed to overcome challenges and realize the full potential of these targets.
- Understanding DCUN1D1's structure and function is key to developing effective cancer therapies.
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