Das Provas, Taube Joseph H
Department of Biology, Baylor University, Waco, TX 76706, USA.
Cancers (Basel). 2020 Sep 29;12(10):2792. doi: 10.3390/cancers12102792.
Properly timed addition and removal of histone 3 lysine 27 tri-methylation (H3K27me3) is critical for enabling proper differentiation throughout all stages of development and, likewise, can guide carcinoma cells into altered differentiation states which correspond to poor prognoses and treatment evasion. In early embryonic stages, H3K27me3 is invoked to silence genes and restrict cell fate. Not surprisingly, mutation or altered functionality in the enzymes that regulate this pathway results in aberrant methylation or demethylation that can lead to malignancy. Likewise, changes in expression or activity of these enzymes impact cellular plasticity, metastasis, and treatment evasion. This review focuses on current knowledge regarding methylation and de-methylation of H3K27 in cancer initiation and cancer cell plasticity.
组蛋白3赖氨酸27三甲基化(H3K27me3)的适时添加和去除对于在发育的各个阶段实现正常分化至关重要,同样,它也可以引导癌细胞进入改变的分化状态,这些状态与预后不良和逃避治疗相对应。在胚胎早期阶段,H3K27me3被用于使基因沉默并限制细胞命运。不出所料,调节该途径的酶发生突变或功能改变会导致异常甲基化或去甲基化,进而可能引发恶性肿瘤。同样,这些酶的表达或活性变化会影响细胞可塑性、转移和逃避治疗。本综述重点关注关于H3K27甲基化和去甲基化在癌症起始和癌细胞可塑性方面的现有知识。