...
首页> 外文期刊>Biological & pharmaceutical bulletin >Extract from Serenoa repens suppresses the invasion activity of human urological cancer cells by inhibiting urokinase-type plasminogen activator.
【24h】

Extract from Serenoa repens suppresses the invasion activity of human urological cancer cells by inhibiting urokinase-type plasminogen activator.

机译:Serenoa repens的提取物通过抑制尿激酶型纤溶酶原激活物来抑制人泌尿外科癌细胞的侵袭活性。

获取原文
获取原文并翻译 | 示例
           

摘要

We used three human urological cancer cell lines, PC-3, LNCaP and SKRC-1, to investigate the effects of the extract from Serenoa repens (Palmae) on tumor cell invasion. The invasion activity of these cell lines was determined in vitro using a Transwell cell-culture chamber. The invasion activity of PC-3 cells into Matrigel was effectively suppressed by the extract at the concentration range of 1-10 microg/ml, while that of LNCaP and SKRC-1 cells was unaffected by the extract. The extract did not affect the viability, adhesion ability, or motility of the cell lines. uPA is more strongly expressed on the membrane fraction of PC-3 cells than that of LNCaP or SKRC-1 cells. The purified uPA activity is inhibited by the extract from S. repens in a dose-dependent manner, suggesting that the suppression of PC-3 cell invasion by the extract is based on an inhibition of the uPA activity which is necessary for tumor cell invasion. These data suggest that the extract from S. repens specifically inhibits the uPA activity and may therefore be useful for the therapeutic treatment of prostate cancer.
机译:我们使用了三种人类泌尿外科癌细胞系PC-3,LNCaP和SKRC-1,来研究Serenoa repens(Palmae)提取物对肿瘤细胞侵袭的影响。使用Transwell细胞培养室在体外确定这些细胞系的侵袭活性。提取物在1-10μg/ ml的浓度范围内可有效抑制PC-3细胞侵袭基质胶,而LNCaP和SKRC-1细胞的侵染活性不受提取物的影响。提取物不影响细胞系的活力,粘附能力或运动性。与LNCaP或SKRC-1细胞相比,uPA在PC-3细胞的膜级分上表达更强。纯化的uPA活性被白毛链球菌的提取物以剂量依赖的方式抑制,这表明提取物对PC-3细胞入侵的抑制是基于对肿瘤细胞入侵所必需的uPA活性的抑制。这些数据表明,来自链球菌的提取物特异性地抑制uPA活性,因此可用于前列腺癌的治疗。

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