Xi Qinghua, Huang Menghui, Wang Yingying, Zhong Jianxin, Liu Rong, Xu Guiqin, Jiang Lifei, Wang Juan, Fang Zheng, Yang Shuyun
Department of Obstetrics and Gynecology, Affiliated Hospital of Nantong University, Jiangsu Province Key Laboratory for Information and Molecular Drug Target, Nantong University, Nantong, 226001, Jiangsu Province, China.
Tumour Biol. 2015 Jul;36(7):4939-48. doi: 10.1007/s13277-015-3141-8. Epub 2015 Apr 25.
Overexpression of cyclin-dependent kinase 1 (CDK1) has been noted to correlation with several human cancers. However, the effects of CDK1 on ovarian cancer development remain unclear. The aim of this study was to examine the effect of CDK1 and related mechanism in the proliferation and resistance to chemotherapeutic drugs of epithelial ovarian cancer (EOC). Immunohistochemical analysis was performed in 119 human ovarian cancer samples, and the data were correlated with clinicopathologic features. Furthermore, Western blot analysis was performed for CDK1 in EOC samples and cell lines to evaluate their protein levels and molecular interaction. Kaplan-Meier survival analysis showed that strong expression of CDK1 exhibited a significant correlation with poor prognosis in human EOC (P = 0.02). Meanwhile, we found that knockdown CDK1 by shCDK1 promoted the apoptosis rate and increased the sensitivity to chemotherapy drugs. Thus, CDK1 might serve as a prognostic marker, and it might be of great value for experimental therapies in EOC.
细胞周期蛋白依赖性激酶1(CDK1)的过表达已被指出与多种人类癌症相关。然而,CDK1对卵巢癌发展的影响仍不清楚。本研究的目的是探讨CDK1在上皮性卵巢癌(EOC)增殖和对化疗药物耐药中的作用及相关机制。对119例人类卵巢癌样本进行免疫组织化学分析,并将数据与临床病理特征相关联。此外,对EOC样本和细胞系中的CDK1进行蛋白质印迹分析,以评估其蛋白水平和分子相互作用。Kaplan-Meier生存分析表明,CDK1的强表达与人类EOC的不良预后显著相关(P = 0.02)。同时,我们发现通过shCDK1敲低CDK1可提高凋亡率并增加对化疗药物的敏感性。因此,CDK1可能作为一种预后标志物,对EOC的实验性治疗可能具有重要价值。