胶质瘤
细胞周期
癌症研究
基因敲除
生物
流式细胞术
癌基因
细胞生长
小干扰RNA
免疫组织化学
细胞
细胞凋亡
转染
分子生物学
细胞培养
免疫学
生物化学
遗传学
作者
Wenjuan Chen,Li Zhang,Yan Wang,Jie Sun,Donglin Wang,Shaochen Fan,Na Ban,Junya Zhu,Bin Ji,Yuchan Wang
出处
期刊:Tumor Biology
[SAGE Publishing]
日期:2015-10-21
卷期号:37 (3): 4093-4103
被引量:22
标识
DOI:10.1007/s13277-015-4088-5
摘要
Cell division cycle 5-like (CDC5L) protein is a cell cycle regulator of the G2/M transition and has been reported to participate in the catalytic step of pre-messenger RNA (mRNA) splicing and DNA damage repair. Recently, it was also found to act as a candidate oncogene in osteosarcoma and cervical tumors. However, the role of CDC5L expression in tumor biology was still unclear. Here, we analyzed the expression and clinical significance of CDC5L in gliomas. The expression of CDC5L in fresh glioma tissues and paraffin-embedded slices was evaluated by western blot and immunohistochemistry, respectively. We found that CDC5L was highly expressed in glioma tissues. The expression of CDC5L was significantly associated with glioma pathology grade and Ki-67 expression. Univariate and multivariate analyses showed that high CDC5L expression was an independent prognostic factor for glioma patients' survival. To determine whether CDC5L could regulate the proliferation of glioma cells, we transfected glioma cells with interfering RNA target CDC5L, then investigated cell proliferation with cell counting kit (CCK)-8, flow cytometry assays and colony formation analyses. Our results indicated that knockdown of CDC5L would inhibit proliferation of glioma cells. Besides, reduced expression of CDC5L could induce the apoptosis of glioma cells. These findings suggested that CDC5L might play an important role in glioma and thus be a promising therapeutic target of glioma.
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