Novel inhibitors of the STAT3 signaling pathway: an updated patent review (2014-present)
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Published on: January 22, 2019
Feng Wang1, Xin-Yu Cao1, Guo-Qiang Lin1
1The Research Center of Chiral Drugs, Shanghai Frontiers Science Center for Traditional Chinese Medicine Chemical Biology and Innovation Research Institute of Traditional Chinese Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai, Xuhui, China.
Introduction:
STAT3 is a critical transcription factor that transmits signals from the cell surface to the nucleus, thus influencing the transcriptional regulation of some oncogenes. The inhibition of the activation of STAT3 is considered a promising strategy for cancer therapy. Numerous STAT3 inhibitors bearing different scaffolds have been reported to date, with a few of them having been considered in clinical trials.
Areas Covered:
This review summarizes the advances on STAT3 inhibitors with different structural skeletons, focusing on the structure-activity relationships in the related patent literature published from 2014 to date.
Expert Opinion:
Since the X-ray crystal structure of STAT3β homo dimer bound to DNA was solved in 1998, the development of STAT3 inhibitors has gone through a boom in recent years. However, none of them have been approved for marketing, probably due to the complex biological functions of the STAT3 signaling pathway, including its character and the poor drug-like physicochemical properties of its inhibitors. Nonetheless, targeting STAT3 continues to be an exciting field for the development of anti-tumor agents along with the emergence of new STAT3 inhibitors with unique mechanisms of action.
Insights
Signal transducer and activator of transcription 3 (STAT3) inhibitors are promising cancer therapies. This review covers recent advances in STAT3 inhibitor development and structure-activity relationships from patent literature.
Area of Science:
- Molecular Biology
- Oncology
- Medicinal Chemistry
Background:
- Signal transducer and activator of transcription 3 (STAT3) is a key transcription factor regulating oncogenes.
- Inhibiting STAT3 activation is a promising cancer therapeutic strategy.
- Despite extensive research, no STAT3 inhibitors have reached the market.
Purpose of the Study:
- To review recent advancements in STAT3 inhibitors.
- To focus on structure-activity relationships (SAR) within patent literature.
- To cover developments from 2014 to the present.
Main Methods:
- Comprehensive literature search of patent databases.
- Analysis of STAT3 inhibitors reported in patents.
- Evaluation of structure-activity relationships.
Main Results:
- Numerous STAT3 inhibitors with diverse scaffolds have been developed.
- Several inhibitors have advanced to clinical trials.
- Emerging inhibitors exhibit novel mechanisms of action.
Conclusions:
- Targeting STAT3 remains a vital area for anti-cancer drug development.
- Challenges include STAT3 pathway complexity and inhibitor drug-like properties.
- Continued research into novel STAT3 inhibitors is warranted.
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