Epigenetic therapy using histone deacetylase (HDAC) inhibitors has become an attractive project in new drug development. However, DNA methylation and histone acetylation are important epigenetic ways to regulate the occurrence and development of leukemia. Given previous studies, N-(2-aminophenyl)benzamide acridine (8a), as a histone deacetylase 1 (HDAC1) inhibitor, induces apoptosis and shows significant anti-proliferative activity against histiocytic lymphoma U937 cells. HDAC1 plays a role in the nucleus, which we confirmed by finding that 8a entered the nucleus. Subsequently, we verified that 8a mainly passes through the endogenous (mitochondrial) pathway to induce cell apoptosis. From the protein interaction data, we found that 8a also affected the expression of DNA methyltransferase 1 (DNMT1). Therefore, an experiment was performed to assess the binding of 8a to DNMT1 at the molecular and cellular levels. We found that the binding strength of 8a to DNMT1 enhanced in a dose-dependent manner. Additionally, 8a inhibits the expression of DNMT1 mRNA and its protein. These findings suggested that the anti-proliferative and pro-apoptotic activities of 8a against leukemia cells were achieved by targeting HDAC1 and DNMT1.
Keyphrases
- histone deacetylase
- dna methylation
- binding protein
- genome wide
- gene expression
- induced apoptosis
- cell death
- cell cycle arrest
- poor prognosis
- anti inflammatory
- acute myeloid leukemia
- bone marrow
- oxidative stress
- risk assessment
- copy number
- cell proliferation
- protein protein
- machine learning
- endoplasmic reticulum stress
- stem cells
- mesenchymal stem cells
- signaling pathway
- cancer therapy
- drug delivery
- diffuse large b cell lymphoma
- amino acid
- quality improvement
- small molecule
- dna binding
- pi k akt
- big data
- artificial intelligence
- cell free