Department of Medical Genetics and Skeletal Rare Diseases, Rizzoli Orthopaedic Institute, 40136 Bologna, Italy.
Clin Genet. 2010 Dec;78(6):507-16. doi: 10.1111/j.1399-0004.2010.01490.x.
Multiple osteochondroma (MO) is a rare skeletal disease characterized by the formation of multiple benign cartilage-capped bone tumors; in 1-5% of patients, a malignant transformation into peripheral chondrosarcoma may occur. This disorder is characterized by a large spectrum of germline mutations scattered along EXT1/EXT2 genes, the presence of a significant percentage of patients without alterations in EXT genes, and a large phenotypic variability. The molecular basis of MO genetic and clinical heterogeneity, including the causes underlying malignant transformation, is currently unknown. This leads to the lack of appropriate diagnostic/prognostic markers as well as of therapeutic options. Recently, specific microRNAs (miRNAs) were reported to be involved in chondrogenesis and inflammatory cartilage diseases. We therefore hypothesized a role for microRNAs in cartilaginous tumors and investigated microRNA expression in osteochondroma and normal cartilage tissues to evaluate whether they could affect osteochondromas onset and/or clinical manifestations. Our results indicate that miRNAs differentially expressed in MO samples may hamper the molecular signaling responsible for normal differentiation of chondrocytes, contributing to pathogenesis and clinical outcome. Although further studies are needed to validate our observations and to identify targets of miRNAs, this is the first study reporting on miRNA expression in growth plate and its comparison with pathological conditions.
多发性骨软骨瘤(MO)是一种罕见的骨骼疾病,其特征是形成多个良性软骨帽骨肿瘤;在 1-5%的患者中,可能会恶变为外周软骨肉瘤。该疾病的特征是存在大量散在的胚系突变沿 EXT1/EXT2 基因,存在很大比例的患者 EXT 基因无改变,且表型具有很大的可变性。MO 的遗传和临床异质性的分子基础,包括恶性转化的原因,目前尚不清楚。这导致缺乏适当的诊断/预后标志物以及治疗选择。最近,有研究报道特定的 microRNAs(miRNAs)参与软骨生成和炎症性软骨疾病。因此,我们假设 microRNAs 在软骨肿瘤中发挥作用,并研究了骨软骨瘤和正常软骨组织中的 microRNA 表达,以评估它们是否会影响骨软骨瘤的发生和/或临床表现。我们的结果表明,在 MO 样本中差异表达的 miRNAs 可能会阻碍负责软骨细胞正常分化的分子信号,从而促进发病机制和临床结果。尽管需要进一步的研究来验证我们的观察结果并确定 miRNAs 的靶标,但这是第一项关于生长板中 microRNA 表达及其与病理状况比较的研究。