Potratz Jenny, Jürgens Heribert, Craft Alan, Dirksen Uta
Pediatric Hematology and Oncology, University Children's Hospital Münster, Münster, Germany.
Pediatr Hematol Oncol. 2012 Feb;29(1):12-27. doi: 10.3109/08880018.2011.627582.
Ewing sarcoma, a rare malignancy of childhood and adolescence, has attracted wide research interest. Tumor-specific chromosomal translocations generate aberrant EWS-ETS transcription factors, which alter intracellular signaling networks through gene and protein expression and are considered to be the primary tumor-initiating event. Ewing sarcoma therefore offers insights into principle molecular mechanisms of cancer development and maintenance. Still, despite long-standing research, biology-based targeted treatment strategies for Ewing sarcoma are only beginning to emerge. This article provides an overview of the biological basis and putative targeted treatment options.
尤因肉瘤是儿童和青少年时期的一种罕见恶性肿瘤,已引起广泛的研究兴趣。肿瘤特异性染色体易位产生异常的EWS-ETS转录因子,这些转录因子通过基因和蛋白质表达改变细胞内信号网络,被认为是主要的肿瘤起始事件。因此,尤因肉瘤为癌症发生和维持的主要分子机制提供了见解。尽管进行了长期研究,但基于生物学的尤因肉瘤靶向治疗策略才刚刚开始出现。本文概述了其生物学基础和假定的靶向治疗选择。