Jung Inkyung, An Jungeun, Ko Myunggon
Department of Biological Sciences, Ulsan National Institute of Science and Technology, Ulsan 44919, Republic of Korea.
Department of Life Sciences, Jeonbuk National University, Jeonju 54896, Republic of Korea.
Biomedicines. 2023 Feb 21;11(3):654. doi: 10.3390/biomedicines11030654.
Epigenetic modifications are crucial regulators of gene expression that critically impact cell lineage differentiation, survival, and proliferation, and dysregulations are commonly observed in various cancers. The aberrantly modified epigenome confers unique features on tumor cells, including sustained proliferative potential, resistance to growth-suppressive or cell death signals, augmented replicative immortality, invasion, and metastasis. As a result, epigenetic abnormalities exhibit significant impacts on all stages of oncogenesis from its onset to progression to metastasis. Among various epigenetic mechanisms in mammals, DNA cytosine methylation-demethylation is recurrently disrupted in cancers. Due to its inherent reversibility, targeting DNA methylation dynamics has gained tremendous attention as a promising therapeutic option that can ameliorate the effects of cancer-specific epigenetic abnormalities by restoring normal conditions. Various small molecules targeting DNA (de)methylation regulators have been developed as potential cancer therapeutics, some of which are approved for usage in clinics. Clinical trials of many other molecules are underway for both hematological malignancies and solid tumors. In this review, we discuss the DNA methylation/demethylation pathway as a promising target for therapeutic intervention in cancer and highlight the development of various epigenetic drugs targeting DNA-modifying enzymes such as DNA methyltransferases (DNMTs) and ten-eleven translocation (TET) enzymes.
表观遗传修饰是基因表达的关键调节因子,对细胞谱系分化、存活和增殖具有至关重要的影响,并且在各种癌症中普遍观察到失调现象。异常修饰的表观基因组赋予肿瘤细胞独特的特征,包括持续的增殖潜能、对生长抑制或细胞死亡信号的抗性、增强的复制永生性、侵袭和转移。因此,表观遗传异常在肿瘤发生从起始到进展再到转移的所有阶段都表现出重大影响。在哺乳动物的各种表观遗传机制中,DNA胞嘧啶甲基化-去甲基化在癌症中经常被破坏。由于其固有的可逆性,靶向DNA甲基化动态变化作为一种有前景的治疗选择受到了极大关注,它可以通过恢复正常状态来改善癌症特异性表观遗传异常的影响。各种靶向DNA(去)甲基化调节因子的小分子已被开发为潜在的癌症治疗药物,其中一些已被批准用于临床。许多其他分子针对血液系统恶性肿瘤和实体瘤的临床试验正在进行中。在本综述中,我们讨论了DNA甲基化/去甲基化途径作为癌症治疗干预的一个有前景的靶点,并强调了针对DNA修饰酶如DNA甲基转移酶(DNMTs)和十一-易位(TET)酶的各种表观遗传药物的开发。