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USP6 and CDH11 Oncogenes Identify the Neoplastic Cell in Primary Aneurysmal Bone Cysts and Are Absent in So-Called Secondary Aneurysmal Bone Cysts

机译:USP6和CDH11致癌基因识别原发性动脉瘤性骨囊肿中的赘生性细胞,而所谓的继发性动脉瘤性骨囊肿中则不存在

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摘要

Aneurysmal bone cyst (ABC) is a locally recurrent bone lesion that has been regarded as a reactive process. Recently, a neoplastic basis in primary ABC was evidenced by demonstration of clonal chromosome band 17p13 translocations that place the USP6 (TRE2 or TRE17) oncogene under the regulatory influence of the highly active CDH11 promoter. Herein, we report CDH11 and/or USP6 rearrangements in 36 of 52 primary ABCs (69%), of which 10 had CDH11-USP6 fusion, 23 had variant USP6 rearrangements without CDH11 rearrangement, and three had variant CDH11 rearrangements without USP6 rearrangement. USP6 and CDH11 rearrangements were restricted to spindle cells in the ABC and were not found in multinucleated giant cells, inflammatory cells, endothelial cells, or osteoblasts. CDH11 and USP6 rearrangements did not correlate with recurrence-free survival, or with other clinicopathological features. CDH11 and USP6 rearrangements were not found in any of 17 secondary ABC associated with giant cell tumor, chondroblastoma, osteoblastoma, and fibrous dysplasia. These findings demonstrate that primary ABC are mesenchymal neoplasms exhibiting USP6 and/or CDH11 oncogenic rearrangements. By contrast, secondary ABC lack CDH11 and USP6 rearrangements, and although morphological mimics of primary ABC, appear to represent a non-specific morphological pattern of a diverse group of non-ABC neoplasms.
机译:动脉瘤性骨囊肿(ABC)是一种局部复发性骨病变,已被视为反应性过程。最近,通过证明克隆性染色体带17p13易位证明了原发性ABC的肿瘤基础,该染色体易位使USP6(TRE2或TRE17)癌基因处于高活性CDH11启动子的调节作用下。在这里,我们报告CDH11和/或USP6重排在52个原发ABC中的36个(69%)中,其中10个具有CDH11-USP6融合,23个具有USP6变异而没有CDH11重排,三个具有CDH11变异而没有USP6重排。 USP6和CDH11重排仅限于ABC中的纺锤体细胞,在多核巨细胞,炎性细胞,内皮细胞或成骨细胞中未发现。 CDH11和USP6重排与无复发生存或其他临床病理特征无关。在伴有巨细胞瘤,软骨母细胞瘤,成骨细胞瘤和纤维异常增生的17种继发性ABC中,未发现CDH11和USP6重排。这些发现表明原发性ABC是间质性肿瘤,表现出USP6和/或CDH11致癌性重排。相比之下,继发性ABC缺乏CDH11和USP6重排,尽管原发性ABC的形态模拟,似乎代表了多种非ABC肿瘤的非特异性形态学模式。

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