Hypoxia makes EZH2 inhibitor not easy—advances of crosstalk between HIF and EZH2

Zhanya Huang, Yuanjun Tang, Jianlin Zhang, Jiaqi Huang, Rui Cheng, Yunyun Guo, Celina G Kleer, Yuqing Wang, Lixiang Xue
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引用次数: 0

Abstract

Histone methylation plays a crucial role in tumorigenesis. Enhancer of zeste homolog 2 (EZH2) is a histone methyltransferase that regulates chromatin structure and gene expression. EZH2 inhibitors (EZH2is) have been shown to be effective in treating hematologic malignancies, while their effectiveness in solid tumors remains limited. One of the major challenges in the treatment of solid tumors is their hypoxic tumor microenvironment. Hypoxia-inducible factor 1-alpha (HIF-1α) is a key hypoxia responder that interacts with EZH2 to promote tumor progression. Here we discuss the implications of the relationship between EZH2 and hypoxia for expanding the application of EZH2is in solid tumors.
缺氧使 EZH2 抑制剂难以发挥作用--HIF 与 EZH2 之间的相互影响
组蛋白甲基化在肿瘤发生中起着至关重要的作用。泽斯特同源物增强子2(EZH2)是一种组蛋白甲基转移酶,可调节染色质结构和基因表达。EZH2抑制剂(EZH2is)已被证明能有效治疗血液系统恶性肿瘤,但对实体瘤的疗效仍然有限。治疗实体瘤的主要挑战之一是其缺氧的肿瘤微环境。缺氧诱导因子 1-α(HIF-1α)是一种关键的缺氧反应因子,它与 EZH2 相互作用,促进肿瘤的进展。在此,我们将讨论 EZH2 与缺氧之间的关系对扩大 EZH2is 在实体瘤中应用的意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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