Neurosurgery Department, Tangdu Hospital, the Fourth Military Medical University, Xi'an, Shaanxi Province, 710038, China.
Neurosci Lett. 2012 Dec 7;531(2):204-8. doi: 10.1016/j.neulet.2012.10.021. Epub 2012 Oct 26.
MicroRNA-375 (miR-375) is frequently demonstrated to be frequently dysregulated and functions as a tumor suppressor or an oncogene in different cancer types. However, its roles in human gliomas have not been reported. The aim of this study was to investigate the expression pattern and clinical significance of miR-375 in patients with gliomas.
Real-time quantitative RT-PCR assay was performed to detect miR-375 expression in human gliomas and non-neoplastic brain tissues. Then, the association of miR-375 expression with clinicopathological factors and prognosis of glioma patients was also statistically analyzed.
miR-375 expression was significantly decreased on average in glioma tissues relative to non-neoplastic brain tissues (P<0.0001) with ascending pathological grade. Then, the low miR-375 expression in glioma tissues was significantly associated with advanced pathological grade (P=0.003) and low Karnofsky performance score (KPS, P=0.01). Moreover, both univariate and multivariate Cox regression analyses determined that loss of miR-375 expression effectively predicted the decreased overall survival in patients with gliomas.
These findings offer the first convinced evidence that the downregulation of miR-375 expression in human gliomas may play an inhibitory role during the tumor development. This miRNA might function as a candidate unfavorable prognostic marker for human gliomas.
MicroRNA-375(miR-375)在不同类型的癌症中经常被证明存在失调现象,并且可以作为肿瘤抑制因子或癌基因发挥作用。然而,其在人类脑胶质瘤中的作用尚未被报道。本研究旨在探讨 miR-375 在脑胶质瘤患者中的表达模式及其临床意义。
采用实时定量 RT-PCR 检测 miR-375 在人胶质瘤组织和非肿瘤性脑组织中的表达。然后,还对 miR-375 表达与胶质瘤患者临床病理因素和预后的关系进行了统计学分析。
miR-375 在胶质瘤组织中的表达水平明显低于非肿瘤性脑组织(P<0.0001),且随病理分级升高而升高。此外,胶质瘤组织中 miR-375 表达水平较低与高级别病理分级(P=0.003)和较低的 Karnofsky 表现评分(KPS,P=0.01)显著相关。此外,单因素和多因素 Cox 回归分析均确定 miR-375 表达缺失可有效预测胶质瘤患者的总体生存率降低。
这些发现首次提供了令人信服的证据,表明 miR-375 在人胶质瘤中的下调表达可能在肿瘤发生发展中发挥抑制作用。该 miRNA 可能成为人类脑胶质瘤的候选不良预后标志物。