Background: Histone deacetylases (HDACs) are critical epigenetic modulators involved in regulating various molecular mechanisms essential for cell development and growth. Alterations in HDAC activity have been linked to the progression of numerous cancers, including lymphoma. Over the past decade, the FDA has approved several HDAC inhibitors for lymphoma treatment, leading to heightened interest in this emerging class of drugs. Methods: In our research, we developed a novel HDAC inhibitor that exhibits high selectivity for class I HDACs. Results: Our in vitro findings indicate that treating lymphoma/leukemia cells with this inhibitor results in a marked suppression of cell growth and promotes apoptosis, while leaving the cell cycle unaffected. Conclusions: We propose that our new inhibitor, named eimbinostat, holds significant promise as a potential therapeutic agent for the treatment of hematologic malignancies such as lymphoma or leukemia.
New and Effective Inhibitor of Class I HDACs, Eimbinostat, Reduces the Growth of Hematologic Cancer Cells and Triggers Apoptosis.
新型高效 I 类 HDAC 抑制剂 Eimbinostat 可减少血液癌细胞的生长并触发细胞凋亡
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作者:Spirin Pavel, Vedernikova Valeria, Volkava Tatsiana, Morozov Alexey, Kleymenova Alla, Zemskaya Anastasia, Shyrokova Lena, Porozov Yuri, Glumakova Ksenia, Lebedev Timofey, Kozlov Maxim, Prassolov Vladimir
| 期刊: | Pharmaceutics | 影响因子: | 5.500 |
| 时间: | 2025 | 起止号: | 2025 Mar 25; 17(4):416 |
| doi: | 10.3390/pharmaceutics17040416 | 研究方向: | 细胞生物学 |
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