Chidamide: Targeting epigenetic regulation in the treatment of hematological malignancy.
Han-Yu CaoLing LiSheng-Li XueHai-Ping DaiPublished in: Hematological oncology (2022)
Epigenetic alterations frequently participate in the onset of hematological malignancies. Histone deacetylases (HDACs) are essential for regulating gene transcription and various signaling pathways. Targeting HDACs has become a novel treatment option for hematological malignancies. Chidamide is the first oral selective HDAC inhibitor for HDAC1, HDAC2, HDAC3, and HDAC10 and was first approved for the treatment of R/R peripheral T-cell lymphoma by the China Food and Drug Administration in 2014. Chidamide was also approved under the name Hiyasta (HBI-8000) in Japan in 2021. In vitro studies revealed that chidamide could inhibit proliferation and induce apoptosis via cell cycle arrest and the regulation of apoptotic proteins. In clinical studies, chidamide was also efficacious in multiple myeloma, acute leukemia and myelodysplastic syndrome. This review includes reported experimental and clinical data on chidamide monotherapy or chidamide treatment in combination with chemotherapy for various hematological malignancies, offering a rationale for the renewed exploration of this drug.
Keyphrases
- cell cycle arrest
- cell death
- drug administration
- signaling pathway
- combination therapy
- clinical trial
- histone deacetylase
- squamous cell carcinoma
- dna methylation
- gene expression
- machine learning
- radiation therapy
- randomized controlled trial
- deep learning
- drug delivery
- cancer therapy
- climate change
- locally advanced
- rectal cancer
- study protocol
- artificial intelligence
- big data
- anti inflammatory
- case control
- genome wide analysis