首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Caffeic Acid Phenethyl Ester Induces N-myc Downstream Regulated Gene 1 to Inhibit Cell Proliferation and Invasion of Human Nasopharyngeal Cancer Cells
【2h】

Caffeic Acid Phenethyl Ester Induces N-myc Downstream Regulated Gene 1 to Inhibit Cell Proliferation and Invasion of Human Nasopharyngeal Cancer Cells

机译:咖啡酸苯乙基酯诱导N-myc下游调节基因1抑制人鼻咽癌细胞的增殖和侵袭

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

Caffeic acid phenethyl ester (CAPE), a bioactive component extracted from propolis, is widely studied due to its anti-cancer effect. Nasopharyngeal carcinoma (NPC) is distinct from other head and neck carcinomas and has a high risk of distant metastases. N-myc downstream regulated gene 1 (NDRG1) is demonstrated as a tumor suppressor gene in several cancers. Our result showed that CAPE treatment could repress NPC cell growth, through induction of S phase cell cycle arrest, and invasion. CAPE treatment stimulated NDRG1 expression in NPC cells. NDRG1 knockdown increased NPC cell proliferation and invasion and rendered NPC cells less responsive to CAPE growth-inhibiting effect, indicating CAPE repressed NPC cell growth partly through NDRG1indcution. CAPE treatment increased phosphorylation of ERK, JNK, and p38 in a dose- and time-dependent manner. Pre-treatments by inhibitors of ERK (PD0325901), JNK (SP600125), or p38 (SB201290), respectively, all could partly inhibit the CAPE effect on NDRG1 induction in NPC cells. Further, STAT3 activity was also repressed by CAPE in NPC cells. In summary, CAPE attenuates NPC cell proliferation and invasion by upregulating NDRG1 expression via MAPK pathway and by inhibiting phosphorylation of STAT3. Considering the poor prognosis of NPC patients with metastasis, CAPE could be a promising agent against NPC.
机译:从蜂胶中提取的生物活性成分咖啡酸苯乙酯(CAPE)由于具有抗癌作用而被广泛研究。鼻咽癌(NPC)与其他头颈癌不同,具有远处转移的高风险。 N-myc下游调控基因1(NDRG1)被证明是几种癌症中的抑癌基因。我们的结果表明,CAPE处理可通过诱导S期细胞周期阻滞和侵袭来抑制NPC细胞的生长。 CAPE处理刺激了NPC细胞中NDRG1的表达。 NDRG1敲低增加了NPC细胞的增殖和侵袭,并使NPC细胞对CAPE生长抑制作用的响应降低,表明CAPE部分抑制了NPC细胞的生长,主要是通过NDRG1抑制。 CAPE处理以剂量和时间依赖性方式增加ERK,JNK和p38的磷酸化。分别通过ERK(PD0325901),JNK(SP600125)或p38(SB201290)抑制剂进行的预处理均可以部分抑制CAPE对NPC细胞中NDRG1诱导的影响。此外,CAP3还在NPC细胞中抑制了STAT3活性。总之,CAPE通过经由MAPK途径上调NDRG1的表达并抑制STAT3的磷酸化来减弱NPC细胞的增殖和侵袭。考虑到NPC转移患者的预后较差,CAPE可能是抗NPC的有前途的药物。

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