Pédiatrie Onco-Hématologie, CHRU Hautepierre, Strasbourg, France.
Transl Oncol. 2010 Dec 1;3(6):344-53. doi: 10.1593/tlo.10169.
TWIST and adenomatosis polyposis coli (APC) are critical signaling factors in normal bone development. In previous studies examining a homogeneously treated cohort of pediatric osteosarcoma patients, we reported the frequent and concurrent loss of both TWIST and APC genes. On these bases, we created a related animal model to further explore the oncogenic cooperation between these two genes. We performed intercrosses between twist-null/+ and Apc1638N/+ mice and studied their progeny. The Apc1638N/+;twistnull/+ mice developed bone abnormalities observed by macroscopic skeletal analyses and in vivo imaging. Complementary histologic, cellular, and molecular analyses were used to characterize the identified bone tumors, including cell culture and immunofluorescence of bone differentiation markers. Spontaneous localized malignant bone tumors were frequently identified in Apc1638N/+;twist-null/+ mice by in vivo imaging evaluation and histologic analyses. These tumors possessed several features similar to those observed in human localized osteosarcomas. In particular, the murine tumors presented with fibroblastic, chondroblastic, and osteoblastic osteosarcoma histologies, as well as mixtures of these subtypes. In addition, cellular analyses and bone differentiation markers detected by immunofluorescence on tumor sections reproduced most murine and human osteosarcoma characteristics. For example, the early bone differentiation marker Runx2, interacting physically with hypophosphorylated pRb, was undetectable in these murine osteosarcomas, whereas phosphorylated retinoblastoma was abundant in the osteoblastic and chondroblastic tumor subtypes. These characteristics, similar to those observed in human osteosarcomas, indicated that our animal model may be a powerful tool to further understand the development of localized osteosarcoma.
TWIST 和腺瘤性结肠息肉病基因(APC)是正常骨骼发育过程中的关键信号因子。在之前研究分析一组经同种方法治疗的儿童骨肉瘤患者时,我们报道了 TWIST 和 APC 基因的频繁且同时缺失。基于这些发现,我们建立了一个相关的动物模型来进一步探究这两个基因的致癌协同作用。我们将 TWIST 基因敲除杂合子(twist-null/+)和 APC1638N 基因杂合子(Apc1638N/+)的小鼠进行杂交,并对其后代进行研究。Apc1638N/+;twistnull/+ 小鼠出现了肉眼可见的骨骼异常和体内影像学改变。我们采用补充的组织学、细胞学和分子学分析方法来对鉴定出的骨肿瘤进行特征描述,包括骨分化标志物的细胞培养和免疫荧光检测。通过体内影像学评估和组织学分析,我们在 Apc1638N/+;twist-null/+ 小鼠中经常发现自发性局部恶性骨肿瘤。这些肿瘤具有与人类局部骨肉瘤相似的特征。具体而言,这些小鼠肿瘤呈现出成纤维细胞性、软骨母细胞性和骨母细胞性骨肉瘤组织学特征,以及这些亚型的混合。此外,肿瘤组织切片的细胞分析和免疫荧光检测到的骨分化标志物重现了大多数人类和小鼠骨肉瘤的特征。例如,与低磷酸化 pRb 相互作用的早期骨分化标志物 Runx2 在这些小鼠骨肉瘤中无法检测到,而磷酸化视网膜母细胞瘤在成骨细胞性和软骨母细胞性肿瘤亚型中丰富存在。这些与人类骨肉瘤观察到的特征相似,表明我们的动物模型可能是进一步了解局部骨肉瘤发生发展的有力工具。