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Epigenetic regulation of the human telomerase reverse transciptase gene: A potential therapeutic target for the treatment of leukemia (Review)

机译:人端粒酶逆转录酶基因的表观遗传调控:白血病的潜在治疗靶点(综述)

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摘要

Telomerase activation is a critical step in human carcinogenesis through the maintenance of telomeres. Telomerase activity is primarily regulated by the human telomerase reverse transcriptase gene (hTERT), thus, an improved understanding of the transcriptional control of hTERT may provide potential therapeutic targets for the treatment of leukemia and other forms of cancer. Epigenetic modulation, a significant regulatory process in cell biology, has recently been shown to be involved in the regulation of the hTERT gene. Moreover, several epigenetic modifiers, including DNA methyltransferase (DNMT) and histone deacetylase (HDAC) inhibitors, are now in pre- and early clinical trials of leukemia as monotherapies or in combination with other drugs, and have achieved significant clinical success. In the present review, the epigenetic mechanisms associated with telomerase activity in leukemia, and the therapeutic potential of an antitelomerase strategy that combines epigenetic modifiers with telomerase hTR subunit small molecule inhibitors are discussed.
机译:端粒酶的激活是人类端粒维持过程中至关重要的一步。端粒酶活性主要受人端粒酶逆转录酶基因(hTERT)调控,因此,对hTERT转录控制的更好了解可能为白血病和其他形式的癌症治疗提供潜在的治疗靶标。表观遗传调控是细胞生物学中重要的调控过程,最近已证明其参与了hTERT基因的调控。此外,几种表观遗传修饰剂,包括DNA甲基转移酶(DNMT)和组蛋白脱乙酰基酶(HDAC)抑制剂,目前正在白血病的早期和早期临床试验中作为单一疗法或与其他药物联合使用,并已取得重大的临床成功。在本综述中,讨论了与白血病中端粒酶活性相关的表观遗传机制,以及将表观遗传修饰剂与端粒酶hTR亚基小分子抑制剂相结合的抗端粒酶策略的治疗潜力。

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