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缺氧使EZH2抑制剂作用受阻——HIF与EZH2相互作用的研究进展

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

作者信息

Huang Zhanya, Tang Yuanjun, Zhang Jianlin, Huang Jiaqi, Cheng Rui, Guo Yunyun, Kleer Celina G, Wang Yuqing, Xue Lixiang

机构信息

Cancer Center of Peking University Third Hospital, Beijing 100191, China.

Center of Basic Medical Research, Institute of Medical Innovation and Research, Peking University Third Hospital, Beijing 100191, China.

出版信息

Life Metab. 2024 Aug;3(4). doi: 10.1093/lifemeta/loae017. Epub 2024 May 6.

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.

摘要

组蛋白甲基化在肿瘤发生中起着至关重要的作用。zeste同源物2增强子(EZH2)是一种调节染色质结构和基因表达的组蛋白甲基转移酶。EZH2抑制剂(EZH2is)已被证明在治疗血液系统恶性肿瘤方面有效,而它们在实体瘤中的有效性仍然有限。实体瘤治疗的主要挑战之一是其缺氧的肿瘤微环境。缺氧诱导因子1α(HIF-1α)是一种关键的缺氧反应因子,它与EZH2相互作用以促进肿瘤进展。在此,我们讨论EZH2与缺氧之间的关系对于扩大EZH2is在实体瘤中的应用的意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c14/11749763/75e8ac225d58/loae017_fig1.jpg

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