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EZH1/2 在血液系统恶性肿瘤中的致癌作用。

Oncogenic roles of enhancer of zeste homolog 1/2 in hematological malignancies.

机构信息

Division of Hematological Malignancy, National Cancer Center Research Institute, Tokyo, Japan.

Department of Orthopaedic Surgery, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.

出版信息

Cancer Sci. 2018 Aug;109(8):2342-2348. doi: 10.1111/cas.13655. Epub 2018 Jun 27.

Abstract

Polycomb group (PcG) proteins regulate the expression of target genes by modulating histone modifications and are representative epigenetic regulators that maintain the stemness of embryonic and hematopoietic stem cells. Histone methyltransferases enhancer of zeste homolog 1 and 2 (EZH1/2), which are subunits of polycomb repressive complexes (PRC), are recurrently mutated or highly expressed in many hematological malignancies. EZH2 has a dual function in tumorigenesis as an oncogene and tumor suppressor gene, and targeting PRC2, in particular EZH1/2, for anticancer therapy has been extensively developed in the clinical setting. Here, we review the oncogenic function of EZH1/2 and introduce new therapeutic drugs targeting these enzymes.

摘要

多梳抑制复合物(PcG)蛋白通过调节组蛋白修饰来调节靶基因的表达,是维持胚胎和造血干细胞干性的代表性表观遗传调节剂。组蛋白甲基转移酶增强子的锌指蛋白 1 和 2(EZH1/2)是多梳抑制复合物(PRC)的亚基,在许多血液恶性肿瘤中经常发生突变或高表达。EZH2 在肿瘤发生中具有双重功能,既是癌基因又是肿瘤抑制基因,针对 PRC2,特别是 EZH1/2 的抗癌治疗在临床环境中得到了广泛的发展。在这里,我们综述了 EZH1/2 的致癌功能,并介绍了针对这些酶的新的治疗药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75fb/6113435/bfd2067fefa9/CAS-109-2342-g001.jpg

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