...
首页> 外文期刊>Molecular Cancer >Interferon regulatory factor 4 binding protein is a novel p53 target gene and suppresses cisplatin-induced apoptosis of breast cancer cells
【24h】

Interferon regulatory factor 4 binding protein is a novel p53 target gene and suppresses cisplatin-induced apoptosis of breast cancer cells

机译:干扰素调节因子4结合蛋白是一种新型的p53靶基因,可抑制顺铂诱导的乳腺癌细胞凋亡

获取原文
           

摘要

Background Our previous work demonstrated that ectopic expression of interferon regulatory factor 4 binding protein (IBP) was correlated with the malignant behaviour of human breast cancer cells. The mechanisms controlling differential expression of IBP in breast cancer still remain unknown. Results To investigate the mechanism of IBP dysregulation in breast cancer, we identified IBP was a novel p53 target gene. IBP expression was negatively regulated by wild-type p53 and was p53 dependently suppressed by DNA damage agent cisplatin. Furthermore, high levels of IBP were found to decrease cisplatin-induced growth suppression and apoptotic cell death, which was associated with decreased p53 activity and imbalanced Bcl-2 family member expression. Conclusions IBP is a novel p53 target gene which suppresses cisplatin-mediated apoptosis of breast cancer cells via negative feedback regulation of the p53 signalling pathway, suggesting IBP may serve as a target for pharmacologic intervention of breast cancer resistant to cisplatin therapy.
机译:背景我们以前的工作表明,干扰素调节因子4结合蛋白(IBP)的异位表达与人类乳腺癌细胞的恶性行为相关。控制IBP在乳腺癌中差异表达的机制仍然未知。结果为研究IBP在乳腺癌中的失调机制,我们确定IBP是一种新型的p53靶基因。 IBP表达受野生型p53负调控,而p53受DNA损伤剂顺铂抑制。此外,发现高水平的IBP可降低顺铂诱导的生长抑制和凋亡细胞死亡,这与p53活性降低和Bcl-2家族成员表达失衡有关。结论IBP是一种新的p53靶基因,可通过p53信号通路的负反馈调节抑制顺铂介导的乳腺癌细胞凋亡,提示IBP可作为抗顺铂治疗乳腺癌的药物干预靶点。

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