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Updated: Mar 22, 2026

Simultaneous Measurement of HDAC1 and HDAC6 Activity in HeLa Cells Using UHPLC-MS
Published on: August 10, 2017
Use of class I histone deacetylase inhibitor romidepsin in combination regimens
1a Division of Hematology/Oncology , Northwestern University , Chicago , IL , USA ;
Abstract:
Histone deacetylase (HDAC) inhibitors are epigenetic-modifying agents that have shown promise as anticancer therapies. Several HDAC inhibitors have been approved by the US Food and Drug Administration (FDA) as single-agent therapies to treat T-cell lymphoma. The synergistic combination of HDAC inhibitors with other anticancer agents has the potential to constitute treatment regimens with enhanced efficacy. Romidepsin is a structurally unique, potent, bicyclic class 1 selective HDAC inhibitor approved by the FDA for the treatment of patients with peripheral T-cell lymphoma who have had at least 1 prior therapy and patients with cutaneous T-cell lymphoma who have had at least 1 prior systemic therapy. Here, we review data that support the use of romidepsin in combination with other anticancer agents for the treatment of various malignancies. Promising results have emerged from early clinical studies, supporting the potential for romidepsin combination regimens to constitute safe and effective treatments for cancer.
Insights
Histone deacetylase (HDAC) inhibitors like romidepsin show promise in cancer treatment. Combining romidepsin with other agents may offer safer and more effective cancer therapies.
Area of Science:
- Oncology
- Epigenetics
- Pharmacology
Background:
- Histone deacetylase (HDAC) inhibitors are epigenetic-modifying agents with demonstrated anticancer potential.
- Several HDAC inhibitors are FDA-approved for T-cell lymphoma treatment.
- Combining HDAC inhibitors with other anticancer agents may enhance treatment efficacy.
Purpose of the Study:
- To review data supporting the use of romidepsin in combination with other anticancer agents.
- To explore the potential of romidepsin combination regimens for various malignancies.
Main Methods:
- Review of existing clinical study data.
- Analysis of romidepsin's efficacy in combination therapies.
Main Results:
- Romidepsin is a potent, selective class 1 HDAC inhibitor approved for specific T-cell lymphomas.
- Early clinical studies show promising results for romidepsin combination regimens.
- These combinations suggest potential for enhanced efficacy in treating various cancers.
Conclusions:
- Romidepsin combination regimens demonstrate potential as safe and effective cancer treatments.
- Further research into romidepsin combinations may lead to improved therapeutic strategies for malignancies.
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