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NSD3: Advances in cancer therapeutic potential and inhibitors research
Siyu Xiu1, Xiaowei Chi1, Zhenyu Jia1
1State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing, 100191, PR China.
Abstract:
Nuclear receptor-binding SET domain 3, otherwise known as NSD3, is a member of the group of lysine methyltransferases and is involved in a variety of cellular processes, including transcriptional regulation, DNA damage repair, non-histone related functions and several others. NSD3 gene is mutated or loss of function in a variety of cancers, including breast, lung, pancreatic, and osteosarcoma. These mutations produce dysfunction of the corresponding tumor tissue proteins, leading to tumorigenesis, progression, chemoresistance, and unfavorable prognosis, which suggests that the development of NSD3 probe molecules is important for understanding the specific role of NSD3 in disease and drug discovery. In recent years, NSD3 has been increasingly reported, demonstrating that this target is a very hot epigenetic target. However, the number of NSD3 inhibitors available for cancer therapy is limited and none of the drugs that target NSD3 are currently available on the market. In addition, there are very few reviews describing NSD3. Within this review, we highlight the role of NSD3 in tumorigenesis and the development of NSD3 targeted small-molecule inhibitors over the last decade. We hope that this publication can serve as a guide for the development of potential drug candidates for various diseases in the field of epigenetics, especially for the NSD3 target.
Insights
Nuclear receptor-binding SET domain 3 (NSD3) is a key epigenetic target in cancer. This review highlights NSD3
Area of Science:
- Epigenetics
- Molecular Biology
- Oncology
Background:
- Nuclear receptor-binding SET domain 3 (NSD3) is a lysine methyltransferase implicated in crucial cellular functions.
- NSD3 dysfunction is linked to various cancers, including breast, lung, pancreatic, and osteosarcoma, driving tumorigenesis and chemoresistance.
- Despite its significance, NSD3 remains an underexplored target with limited available inhibitors.
Purpose of the Study:
- To review the role of NSD3 in tumorigenesis.
- To summarize the development of NSD3-targeted small-molecule inhibitors over the past decade.
- To provide a guide for developing novel epigenetic drug candidates targeting NSD3.
Main Methods:
- Literature review focusing on NSD3's role in cancer.
- Analysis of recent advancements in small-molecule inhibitor development for NSD3.
- Synthesis of information on NSD3's involvement in tumorigenesis and therapeutic strategies.
Main Results:
- NSD3 plays a critical role in cancer development and progression.
- Significant progress has been made in identifying and developing NSD3 inhibitors.
- The review consolidates current knowledge on NSD3 as a promising epigenetic target.
Conclusions:
- NSD3 is a vital epigenetic target for cancer therapy.
- Targeting NSD3 with small molecules holds therapeutic potential.
- This review serves as a foundation for future drug discovery efforts against NSD3.
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