Department of Chemical Carcinogenesis, Institute of Chemical Carcinogenesis, Blokhin National Medical Research Center of Oncology, 24 Kashirskoe Shosse, 115478 Moscow, Russia.
Department of Biotechnology and Industrial Pharmacy, Lomonosov Institute of Fine Chemical Technologies, Russian Technological University (MIREA), 86 Vernadsky Avenue, 119571 Moscow, Russia.
Int J Mol Sci. 2023 Aug 17;24(16):12874. doi: 10.3390/ijms241612874.
The development of malignant tumors is caused by a complex combination of genetic mutations and epigenetic alterations, the latter of which are induced by either external environmental factors or signaling disruption following genetic mutations. Some types of cancer demonstrate a significant increase in epigenetic enzymes, and targeting these epigenetic alterations represents a compelling strategy to reverse cell transcriptome to the normal state, improving chemotherapy response. Curaxin CBL0137 is a new potent anticancer drug that has been shown to activate epigenetically silenced genes. However, its detailed effects on the enzymes of the epigenetic system of transcription regulation have not been studied. Here, we report that CBL0137 inhibits the expression of DNA methyltransferase DNMT3a in HeLa TI cells, both at the level of mRNA and protein, and it decreases the level of integral DNA methylation in Ca Ski cells. For the first time, it is shown that CBL0137 decreases the level of BET family proteins, BRD2, BRD3, and BRD4, the key participants in transcription elongation, followed by the corresponding gene expression enhancement. Furthermore, we demonstrate that CBL0137 does not affect the mechanisms of histone acetylation and methylation. The ability of CBL0137 to suppress DNMT3A and BET family proteins should be taken into consideration when combined chemotherapy is applied. Our data demonstrate the potential of CBL0137 to be used in the therapy of tumors with corresponding aberrant epigenetic profiles.
肿瘤的发生是由遗传突变和表观遗传改变的复杂组合引起的,后者是由外部环境因素或遗传突变后的信号中断引起的。某些类型的癌症表现出表观遗传酶的显著增加,针对这些表观遗传改变是一种很有吸引力的策略,可以将细胞转录组逆转到正常状态,提高化疗反应。Curaxin CBL0137 是一种新的有效的抗癌药物,已被证明可以激活表观遗传沉默的基因。然而,其对转录调控的表观遗传系统酶的详细影响尚未研究。在这里,我们报告 CBL0137 抑制 HeLa TI 细胞中 DNA 甲基转移酶 DNMT3a 的表达,无论是在 mRNA 水平还是蛋白水平,并且它降低 Ca Ski 细胞中整体 DNA 甲基化水平。首次表明 CBL0137 降低了 BET 家族蛋白 BRD2、BRD3 和 BRD4 的水平,它们是转录延伸的关键参与者,随后相应基因表达增强。此外,我们证明 CBL0137 不影响组蛋白乙酰化和甲基化的机制。在联合化疗时,应考虑 CBL0137 抑制 DNMT3A 和 BET 家族蛋白的能力。我们的数据表明 CBL0137 具有用于治疗具有相应异常表观遗传谱的肿瘤的潜力。