Key Laboratory for Experimental Teratology of the Ministry of Education and Department of Pathology, Shandong University QiLu Medical College, School of Basic Medical Sciences, Jinan, 250012, China.
Department of Pathology, Shandong University Qilu Hospital, Jinan, 250012, China.
Neoplasia. 2018 Feb;20(2):207-217. doi: 10.1016/j.neo.2017.12.001. Epub 2018 Jan 12.
Risk stratification using molecular features could potentially help distinguish indolent from aggressive prostate cancer (PCa). Mutations in isocitrate dehydrogenase (IDH) acquire an abnormal enzymatic activity, resulting in the production of 2-hydroxyglutarate and alterations in cellular metabolism, histone modification, and DNA methylation. Mutant IDH1 has been identified in various human malignancies, and IDH1R132H constituted the vast majority of mutational events of IDH1. Most recent studies suggested that IDH1 mutations define a methylator subtype in PCa. However, the function of IDH1R132H in PCa development and progression is largely unknown. In this study, we showed that the prevalence of IDH1R132H in Chinese PCa patients is 0.6% (2/336). Of note, IDH1R132H-mutant PCa patients lacked other canonical genomic lesions (e.g., ERG rearrangement, PTEN deletion) that are common in most other PCa patients. The in vitro experiment suggested that IDH1R132H can promote proliferation of benign prostate epithelial cell RWPE-1 when under the situation of low cytokine. It could also promote migration capacity of RWPE-1 cells. Mechanistically, IDH1R132H was an important regulator of insulin-like growth factor 1receptor (IGF1R) by downregulating a set of microRNAs (miR-141-3p, miR-7-5p, miR-223-3p). These microRNAs were repressed by the alteration of epigenetic modification to decrease the enrichment of active marker H3K4me3 or to increase repressive marker H3K27me3 at their promoters. Collectively, we proposed a novel model for an IDH1R132H-microRNAs-IGF1R regulatory axis, which might provide insight into the function of IDH1R132H in PCa development.
使用分子特征进行风险分层可能有助于区分惰性和侵袭性前列腺癌(PCa)。异柠檬酸脱氢酶(IDH)的突变获得异常的酶活性,导致 2-羟基戊二酸的产生和细胞代谢、组蛋白修饰和 DNA 甲基化的改变。突变 IDH1 已在各种人类恶性肿瘤中被鉴定出来,并且 IDH1R132H 构成了 IDH1 突变事件的绝大多数。最近的研究表明,IDH1 突变定义了 PCa 中的一个甲基化亚型。然而,IDH1R132H 在 PCa 发展和进展中的功能在很大程度上尚不清楚。在这项研究中,我们表明 IDH1R132H 在 336 例中国 PCa 患者中的患病率为 0.6%(2/336)。值得注意的是,IDH1R132H 突变型 PCa 患者缺乏其他常见于大多数其他 PCa 患者的典型基因组病变(例如,ERG 重排、PTEN 缺失)。体外实验表明,在低细胞因子的情况下,IDH1R132H 可以促进良性前列腺上皮细胞 RWPE-1 的增殖。它还可以促进 RWPE-1 细胞的迁移能力。在机制上,IDH1R132H 通过下调一组 microRNAs(miR-141-3p、miR-7-5p、miR-223-3p)成为胰岛素样生长因子 1 受体(IGF1R)的重要调节剂。这些 microRNAs 受到表观遗传修饰改变的抑制,以减少其启动子处的活性标记 H3K4me3 的富集或增加抑制性标记 H3K27me3 的富集。总的来说,我们提出了一个新的 IDH1R132H-microRNAs-IGF1R 调节轴模型,该模型可能为 IDH1R132H 在 PCa 发展中的功能提供深入了解。