Hu Hao, Zhang Yi, Cai Xian-Hua, Huang Ji-Feng, Cai Lin
Department of Orthopedics, Wuhan General Hospital of Guangzhou Command; ; Department of Orthopedics, Zhongnan Hospital, Wuhan University, Wuhan, Hubei, P.R. China.
Oncol Lett. 2012 Nov;4(5):1037-1042. doi: 10.3892/ol.2012.866. Epub 2012 Aug 16.
Osteosarcoma (OS) is the most common primary malignant bone tumor, particularly in adolescents and young adults. Early diagnosis remains a significant problem in the clinical treatment of OS as we remain far from a comprehensive understanding of the molecular genetic mechanisms and the biology involved. In addition, microRNAs (miRNAs or miRs), a large family of small non-coding RNAs, may provide a greater understanding of OS as they play a complex role in gene expression regulation in vitro and in vivo. In the current study, the differential expression profiles of miRNAs between OS and osteoblast cell lines were investigated by miRNA microarrays and real-time quantitative PCR (RT-qPCR). A total of 268 miRNAs were identified that were significantly dysregulated in OS compared with the osteoblast cell line, including miR-9, miR-99, miR-195, miR-148a and miR-181a, which had been validated as overexpressed, and miR-143, miR-145, miR-335 and miR-539, which were confirmed to be downregulated. This differential expression may aid future OS diagnosis and prognosis prediction and illustration of the potential mechanisms in the oncogenesis, development and metastasis of OS. Bioinformatic research on these differentially expressed miRNAs suggests that they are able to regulate the biological behaviors of OS in a complex and effective manner. Further study on the function of these miRNAs is likely to provide new insights into OS biology and treatment.
骨肉瘤(OS)是最常见的原发性恶性骨肿瘤,尤其在青少年和年轻成年人中高发。早期诊断在骨肉瘤的临床治疗中仍然是一个重大问题,因为我们对其分子遗传机制和相关生物学过程仍缺乏全面的了解。此外,微小RNA(miRNA或miR)是一类庞大的小型非编码RNA,它们在体外和体内的基因表达调控中发挥着复杂的作用,这可能有助于我们更深入地了解骨肉瘤。在本研究中,通过miRNA微阵列和实时定量PCR(RT-qPCR)研究了骨肉瘤细胞系与成骨细胞系之间miRNA的差异表达谱。共鉴定出268种miRNA在骨肉瘤细胞系中与成骨细胞系相比存在显著失调,其中包括已被验证为过表达的miR-9、miR-99、miR-195、miR-148a和miR-181a,以及被证实下调的miR-143、miR-145、miR-335和miR-539。这种差异表达可能有助于未来骨肉瘤的诊断和预后预测,并阐明骨肉瘤发生、发展和转移的潜在机制。对这些差异表达的miRNA进行生物信息学研究表明,它们能够以复杂而有效的方式调节骨肉瘤的生物学行为。对这些miRNA功能的进一步研究可能为骨肉瘤的生物学和治疗提供新的见解。