Danckwerth F, Wuisman P, Ritter J, Blasius S, Jürgens H, Ozaki T, Winkelmann W
Klinik und Poliklinik für Allgemeine Orthopädie, Westfälischen Wilhelms-Universität Münster.
Klin Padiatr. 1995 Sep-Oct;207(5):298-301. doi: 10.1055/s-2008-1046555.
With a brother and sister, osteosarcoma developed at the age of 11 and 14 respectively. With both there was no previous retinoblastoma or other bone disease with a proclivity to develop osteosarcoma. We discuss possible explanations for familial aggregation of osteosarcoma, citing external or genetic factors. We suggest that it is the retinoblastoma gene RB and the tumor suppressor gene p53 which play an important part in the development of osteosarcoma.
一对兄妹分别在11岁和14岁时患上骨肉瘤。两人之前均无视网膜母细胞瘤或其他易发展为骨肉瘤的骨病。我们讨论了骨肉瘤家族聚集现象的可能解释,列举了外部因素或遗传因素。我们认为视网膜母细胞瘤基因RB和肿瘤抑制基因p53在骨肉瘤的发生发展中起重要作用。