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Bromodomains: are readers right for epigenetic therapy?
1Department of Chemistry, Chemistry Research Laboratory, University of Oxford , Mansfield Road, Oxford, OX2 8JQ, United Kingdom.
ACS Medicinal Chemistry Letters
|June 6, 2014
Summary
Small molecule inhibitors targeting bromodomain proteins offer therapeutic potential in epigenetic processes. Addressing safety concerns is crucial for the clinical success of these epigenetic drugs.
Area of Science:
- Biochemistry
- Epigenetics
- Drug Discovery
Background:
- Bromodomains are protein modules that read acetyl-lysine marks.
- Epigenetic processes are crucial for cellular function and disease.
- Small molecule inhibitors are being developed to target bromodomains.
Purpose of the Study:
- To highlight the therapeutic potential of bromodomain inhibitors.
- To emphasize the importance of safety in epigenetic target modulation.
Main Methods:
- Review of current literature on bromodomain inhibitors.
- Analysis of clinical trial data for existing compounds.
Main Results:
- Intense research interest in developing small molecule bromodomain inhibitors.
- Two bromodomain inhibitors are currently in clinical trials.
Conclusions:
- Bromodomain inhibitors represent a promising therapeutic strategy for epigenetic modulation.
- Ensuring the safety of epigenetic target modulation is paramount for clinical success.
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