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miR-132 缺失预示着原发性骨肉瘤患者预后不良。

Loss of microRNA-132 predicts poor prognosis in patients with primary osteosarcoma.

机构信息

Orthopedics Department, 8th Hospital, Shanghai, China.

出版信息

Mol Cell Biochem. 2013 Sep;381(1-2):9-15. doi: 10.1007/s11010-013-1677-8. Epub 2013 Jun 26.

DOI:10.1007/s11010-013-1677-8
PMID:23801049
Abstract

MicroRNA-132 (miR-132), an angiogenic growth factor inducible microRNA in the endothelium, facilitates pathological angiogenesis. Previous study showed that miR-132 was downregulated in human osteosarcoma. However, its functional attributes associated with tumor progression of osteosarcoma have not been fully elucidated. The aim of this study was to investigate the clinical significance of miR-132 expression in human osteosarcoma. miR-132 expression was detected by quantitative reverse transcription polymerase chain reaction using 166 pairs of osteosarcoma and noncancerous bone tissues. Then, the association of miR-132 expression with clinicopathological factors or survival of osteosarcoma patients was also evaluated. miR-132 expression was significantly lower in osteosarcoma tissues than that in corresponding noncancerous bone tissues (P < 0.001). In addition, miR-132 expression was decreased in the osteosarcoma specimens with advanced clinical stage (P = 0.009), positive distant metastasis (P = 0.006), and poor response to chemotherapy (P = 0.009). Moreover, both the univariate and multivariate analyses showed that osteosarcoma patients with low miR-132 expression had poorer overall and disease-free survival (both P < 0.001), and low miR-132 expression was an independent prognostic factor for both overall (P = 0.001) and disease-free survival (P = 0.006). These findings offer the convinced evidence for the first time that miR-132 may participate in tumor progression of osteosarcoma and loss of miR-132 expression may be a predictor for unfavorable outcome of osteosarcoma patients.

摘要

MicroRNA-132 (miR-132) 是内皮细胞中一种血管生成生长因子诱导的 microRNA,可促进病理性血管生成。先前的研究表明,miR-132 在人骨肉瘤中下调。然而,其与骨肉瘤肿瘤进展相关的功能属性尚未完全阐明。本研究旨在探讨 miR-132 表达在人骨肉瘤中的临床意义。使用 166 对骨肉瘤和非癌性骨组织的定量逆转录聚合酶链反应检测 miR-132 表达。然后,还评估了 miR-132 表达与骨肉瘤患者临床病理因素或生存的关系。miR-132 在骨肉瘤组织中的表达明显低于相应的非癌性骨组织(P < 0.001)。此外,miR-132 在临床分期较晚的骨肉瘤标本中表达降低(P = 0.009),远处转移阳性(P = 0.006),化疗反应不良(P = 0.009)。此外,单因素和多因素分析均表明,miR-132 低表达的骨肉瘤患者总体生存率和无病生存率均较差(均 P < 0.001),miR-132 低表达是总体生存率(P = 0.001)和无病生存率(P = 0.006)的独立预后因素。这些发现首次提供了令人信服的证据,表明 miR-132 可能参与骨肉瘤的肿瘤进展,miR-132 表达缺失可能是骨肉瘤患者不良预后的预测因素。

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