Department of Experimental Medicine 1, Nikolaus-Fiebiger-Center for Molecular Medicine, Friedrich-Alexander-University Erlangen-Nürnberg, Erlangen, Germany.
Institute of Pathology, Friedrich-Alexander-University Erlangen-Nürnberg, Erlangen, Germany.
J Pathol. 2021 Jun;254(2):199-211. doi: 10.1002/path.5659. Epub 2021 May 6.
Osteosarcoma is an often-fatal mesenchyme-derived malignancy in children and young adults. Overexpression of EMT-transcription factors (EMT-TFs) has been associated with poor clinical outcome. Here, we demonstrated that the EMT-TF ZEB1 is able to block osteoblastic differentiation in normal bone development as well as in osteosarcoma cells. Consequently, overexpression of ZEB1 in osteosarcoma characterizes poorly differentiated, highly metastatic subgroups and its depletion induces differentiation of osteosarcoma cells. Overexpression of ZEB1 in osteosarcoma is frequently associated with silencing of the imprinted DLK-DIO3 locus, which encodes for microRNAs targeting ZEB1. Epigenetic reactivation of this locus in osteosarcoma cells reduces ZEB1 expression, induces differentiation, and sensitizes to standard treatment, thus indicating therapeutic options for ZEB1-driven osteosarcomas. © 2021 The Authors. The Journal of Pathology published by John Wiley & Sons, Ltd. on behalf of The Pathological Society of Great Britain and Ireland.
骨肉瘤是一种常见的儿童和青年成人间质来源的恶性肿瘤。 EMT 转录因子(EMT-TFs)的过度表达与不良的临床结局相关。在这里,我们证明 EMT-TF ZEB1 能够阻止正常骨发育和骨肉瘤细胞中的成骨细胞分化。因此,骨肉瘤中 ZEB1 的过表达特征是分化差、转移性高的亚群,其缺失诱导骨肉瘤细胞分化。骨肉瘤中 ZEB1 的过表达常与印迹的 DLK-DIO3 基因座的沉默相关,该基因座编码针对 ZEB1 的 microRNA。骨肉瘤细胞中该基因座的表观遗传再激活降低 ZEB1 的表达,诱导分化,并对标准治疗敏感,因此为 ZEB1 驱动的骨肉瘤提供了治疗选择。 2021 年 The Authors. 《The Journal of Pathology》由 John Wiley & Sons, Ltd. 代表英国和爱尔兰的病理学学会出版。