首页> 外文期刊>Cancer letters >Knockdown of CRM1 inhibits the nuclear export of p27Kip1 phosphorylated at serine 10 and plays a role in the pathogenesis of epithelial ovarian cancer
【24h】

Knockdown of CRM1 inhibits the nuclear export of p27Kip1 phosphorylated at serine 10 and plays a role in the pathogenesis of epithelial ovarian cancer

机译:敲低CRM1抑制在丝氨酸10磷酸化的p27Kip1的核输出,并在上皮性卵巢癌的发病机理中起作用

获取原文
获取原文并翻译 | 示例
           

摘要

In a previous study, the nuclear export protein chromosomal region maintenance (CRM1) was correlated with p27Kip1 in glioma. The aims of the present study were to investigate the expression of CRM1 and pSer10p27 and their functional roles in epithelial ovarian cancer (EOC) tissues. Using immunohistochemical analysis, CRM1 and pSer10p27 expression levels were shown to be associated with histologic stage and grade (P0.05). High CRM1 and pSer10p27 expression levels were prognostic indicators of overall survival (P0.05). Knockdown of CRM1 and pSer10p27 expression arrested cell cycle progression and inhibited the proliferation of SKOV3 cells both in vitro and in vivo. These data support the idea that pSer10p27 and CRM1 play cooperative roles in EOC.
机译:在先前的研究中,核输出蛋白染色体区域的维持(CRM1)与神经胶质瘤中的p27Kip1相关。本研究的目的是调查CRM1和pSer10p27的表达及其在上皮性卵巢癌(EOC)组织中的功能。使用免疫组化分析,CRM1和pSer10p27表达水平与组织学分期和分级相关(P <0.05)。 CRM1和pSer10p27高表达水平是总体生存的预后指标(P <0.05)。敲除CRM1和pSer10p27表达可在体外和体内阻滞细胞周期进程并抑制SKOV3细胞的增殖。这些数据支持pSer10p27和CRM1在EOC中起协同作用的想法。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号