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Published on: May 14, 2016
Histone deacetylase inhibitors and cancer therapy
1University of Glasgow, Glasgow, G12 8QQ, UK. N.LaThangue@bio.gla.ac.uk
Abstract:
Cancer drug development has moved from conventional cytotoxic chemotherapeutics to a more mechanism-based targeted approach towards the common goal of tumour growth arrest. The rapid progress in chromatin research and understanding epigenetic control has supplied a plethora of potential targets for intervention in cancer. Histone deacetylases (HDACs) have been widely implicated in growth and transcriptional control, and inhibition of HDAC activity using small molecules causes apoptosis in tumour cells. Here, we review HDAC inhibitors, together with their current status of clinical development and potential utility in cancer therapy.
Insights
Histone deacetylase (HDAC) inhibitors represent a targeted cancer therapy approach. These drugs induce tumor cell death by modulating epigenetic control, offering new therapeutic strategies.
Area of Science:
- Oncology
- Epigenetics
- Pharmacology
Background:
- Cancer treatment is shifting towards targeted therapies.
- Epigenetic regulation, particularly involving histone deacetylases (HDACs), is crucial in cancer.
- HDACs play a role in cell growth and gene transcription.
Purpose of the Study:
- To review histone deacetylase (HDAC) inhibitors.
- To discuss their clinical development status.
- To evaluate their potential in cancer treatment.
Main Methods:
- Literature review of HDAC inhibitors.
- Analysis of clinical trial data for HDAC inhibitors.
- Assessment of HDAC inhibitor mechanisms in cancer.
Main Results:
- HDAC inhibitors are a class of targeted cancer drugs.
- Inhibition of HDAC activity leads to tumor cell apoptosis.
- Clinical development of HDAC inhibitors is ongoing.
Conclusions:
- HDAC inhibitors show promise as a cancer therapy.
- Targeting epigenetic mechanisms offers a novel therapeutic avenue.
- Further clinical development is warranted for HDAC inhibitors in oncology.
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