Department of Neurosurgery, The Third Xiangya Hospital of Central South University, Changsha 410013, Hunan Province, China.
Biomed Pharmacother. 2017 Oct;94:659-665. doi: 10.1016/j.biopha.2017.07.103. Epub 2017 Aug 5.
Poly(C)-binding protein 2 (PCBP2) has been found to have ambiguous functions in a variety of cancers. However, the specific biological function of PCBP2 and its mechanism in glioblastoma remain unclear. We investigated the expression of PCBP2 in 143 glioblastoma specimens to explore the linkage between PCBP2 expression and clinicopathological parameters as well as clinical significance. Furthermore, the underlying mechanisms of PCBP2 on glioblastoma progression were discussed in vitro.
The transcriptional and translational levels of PCBP2 in 143 glioblastoma patients were detected by quantitative Real-time PCR (qRT-PCR) and western blot. The association of prognostic outcomes and PCBP2 expression was evaluated using Kaplan-Meier analysis.
PCBP2 expression was markedly increased in higher stages of glioblastoma compared with those in lower stages (P<0.001). High expression of PCBP2 was associated with higher clinical stage and histological grade (P<0.001). Further research suggested that PCBP2 upregulation was connected with poorer prognosis in patients with glioblastoma (P<0.001). Moreover, PCBP2 knockdown could significantly decreased the colony formation and invasion capability of glioblastoma cells (P<0.01). Conversely, PCBP2 overexpression could increase the colony formation and invasion capability (P<0.01).
These findings indicated that PCBP2 might be a novel prognostic biomarker and a potential therapeutic target of glioblastoma.
多聚(C)结合蛋白 2(PCBP2)在多种癌症中具有多种功能。然而,PCBP2 在神经胶质瘤中的具体生物学功能及其作用机制尚不清楚。我们检测了 143 例神经胶质瘤标本中 PCBP2 的表达,以探讨 PCBP2 表达与临床病理参数的相关性及其临床意义。此外,还在体外探讨了 PCBP2 对神经胶质瘤进展的潜在机制。
采用实时定量 PCR(qRT-PCR)和 Western blot 检测 143 例神经胶质瘤患者中 PCBP2 的转录和翻译水平。采用 Kaplan-Meier 分析评估预后结局与 PCBP2 表达的关系。
PCBP2 的表达在高级别神经胶质瘤中明显高于低级别神经胶质瘤(P<0.001)。PCBP2 高表达与较高的临床分期和组织学分级相关(P<0.001)。进一步的研究表明,PCBP2 上调与神经胶质瘤患者的预后不良相关(P<0.001)。此外,PCBP2 敲低可显著降低神经胶质瘤细胞的集落形成和侵袭能力(P<0.01)。相反,PCBP2 过表达可增加集落形成和侵袭能力(P<0.01)。
这些发现表明,PCBP2 可能是神经胶质瘤的一种新的预后标志物和潜在的治疗靶点。