首页> 美国卫生研究院文献>other >The Cytotoxic and Pro-Apoptotic Activities of the Novel Fluoropyrimidine F10 Towards Prostate Cancer Cells are Enhanced by Zn2+-Chelation and Inhibiting the Serine Protease Omi/HtrA2
【2h】

The Cytotoxic and Pro-Apoptotic Activities of the Novel Fluoropyrimidine F10 Towards Prostate Cancer Cells are Enhanced by Zn2+-Chelation and Inhibiting the Serine Protease Omi/HtrA2

机译:新型氟嘧啶F10对前列腺癌细胞的细胞毒性和促凋亡活性通过Zn2 +-螯合作用和抑制丝氨酸蛋白酶Omi / HtrA2增强。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

BACKGROUNDIntracellular Zn2+ levels decrease during prostate cancer progression and agents that modulate intracellular Zn2+ are cytotoxic to prostate cancer cells by an incompletely described mechanism. F10 is a new polymeric fluoropyrimidine drug-candidate that displays strong activity with minimal systemic toxicity in pre-clinical models of prostate cancer and other malignancies. The effects of exogenous Zn2+ or Zn2+ chelation for enhancing F10 cytotoxicity are investigated as is the role of Omi/HtrA2, a serine protease that promotes apoptosis in response to cellular stress.
机译:背景技术在前列腺癌进展期间,细胞内Zn 2 + 水平降低,并且通过不完全描述的机制,调节细胞内Zn 2 + 的试剂对前列腺癌细胞具有细胞毒性。 F10是一种新的聚合物氟嘧啶药物候选物,在前列腺癌和其他恶性肿瘤的临床前模型中显示出强大的活性,并且具有最小的全身毒性。研究了外源性Zn 2 + 或Zn 2 + 螯合对增强F10细胞毒性的作用,以及Omi / HtrA2的作用,Omi / HtrA2是一种丝氨酸蛋白酶,可响应于细胞压力。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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