首页> 美国卫生研究院文献>The Iowa Orthopaedic Journal >Of Hedgehogs and Hereditary Bone Tumors: Re-Examination of the Pathogenesis of Osteochondromas
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Of Hedgehogs and Hereditary Bone Tumors: Re-Examination of the Pathogenesis of Osteochondromas

机译:刺猬和遗传性骨肿瘤:骨软骨瘤发病机制的重新检查。

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摘要

The osteochondroma is a common, benign, primary tumor of bone. A mechanism for its pathogenesis has not been identified, but loss of function of EXT genes is implicated in sporadic and hereditary multiple osteochondromas. Recent advances in the understanding of other molecular signaling pathways in the physis cast doubt on the latest pathogenetic theories. These advances are reviewed and used as the basis for a revised theory for pathogenesis: A clone of proliferating chondrocytes without functional EXT1 (or EXT2) expression fails to produce heparan sulfate; lack of heparan sulfate at the cell surface disrupts fibroblast growth factor signaling and Indian hedgehog diffusion, leading to focal overproliferation and adjacent bone collar deficiency, respectively; together these effects are proposed to contribute to osteochondroma pathogenesis.
机译:骨软骨瘤是一种常见的良性骨原发性肿瘤。尚未确定其发病机理,但EXT基因功能丧失与散发性和遗传性多发性骨软骨瘤有关。物理学中对其他分子信号途径的理解的最新进展使人们对最新的致病学理论产生怀疑。综述了这些进展并将其用作修订发病机理的理论的基础:无功能EXT1(或EXT2)表达的增殖性软骨细胞克隆无法产生硫酸乙酰肝素;细胞表面缺乏硫酸乙酰肝素会破坏成纤维细胞生长因子信号传导和印度刺猬扩散,分别导致局灶性过度增殖和邻近的骨环缺乏。这些作用共同被认为有助于骨软骨瘤的发病。

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