Preclinical activity, pharmacodynamic, and pharmacokinetic properties of a selective HDAC6 inhibitor, ACY-1215, in combination with bortezomib in multiple myeloma
Massachusetts General Hospital · Harvard University · +5 more institutions
Abstract
Histone deacetylase (HDAC) enzymatic activity has been linked to the transcription of DNA in cancers including multiple myeloma (MM). Therefore, HDAC inhibitors used alone and in combination are being actively studied as novel therapies in MM. In the present study, we investigated the preclinical activity of ACY-1215, an HDAC6-selective inhibitor, alone and in combination with bortezomib in MM. Low doses of ACY-1215 combined with bortezomib triggered synergistic anti-MM activity, resulting in protracted endoplasmic reticulum stress and apoptosis via activation of caspase-3, caspase-8, and caspase-9 and poly (ADP) ribosome polymerase. In vivo, the anti-MM activity of ACY-1215 in combination with bortezomib was…
Citation impact
- FWCI
- 22.17
- Percentile
- 100%
- References
- 47
Authors
19- LSLoredana SantoCorresponding
Massachusetts General Hospital
- THTeru Hideshima
Harvard University, Dana-Farber Cancer Institute
- ALAndrew L. Kung
Harvard University, Dana-Farber Cancer Institute, Imaging Center
- JTJen‐Chieh Tseng
Harvard University, Dana-Farber Cancer Institute, Imaging Center
- DTDavid Tamang
Acetylon Pharmaceuticals (United States)
Topics & keywords
- Bortezomib
- Pharmacology
- Multiple myeloma
- Medicine
- Cancer research
- Proteasome inhibitor
- Pharmacodynamics
- Histone deacetylase
- Good health and well-being