首页> 美国卫生研究院文献>Genes >Eco-Friendly Formulated Zinc Oxide Nanoparticles: Induction of Cell Cycle Arrest and Apoptosis in the MCF-7 Cancer Cell Line
【2h】

Eco-Friendly Formulated Zinc Oxide Nanoparticles: Induction of Cell Cycle Arrest and Apoptosis in the MCF-7 Cancer Cell Line

机译:环保配方的氧化锌纳米颗粒:MCF-7癌细胞系中细胞周期阻滞和凋亡的诱导。

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

Green products have strong potential in the discovery and development of unique drugs. Zinc oxide nanoparticles (ZnO NPs) have been observed to have powerful cytotoxicity against cells that cause breast cancer. The present study aims to examine the cell cycle profile, status of cell death, and pathways of apoptosis in breast cancer cells (MCF-7) treated with biosynthesized ZnO NPs. The anti-proliferative activity of ZnO NPs was determined using MTT assay. Cell cycle analysis and the mode of cell death were evaluated using a flow cytometry instrument. Quantitative real-time-PCR (qRT-PCR) was employed to investigate the expression of apoptosis in MCF-7 cells. ZnO NPs were cytotoxic to the MCF-7 cells in a dose-dependent manner. The 50% growth inhibition concentration (IC50) of ZnO NPs at 24 h was 121 µg/mL. Cell cycle analysis revealed that ZnO NPs induced sub-G1 phase (apoptosis), with values of 1.87% at 0 μg/mL (control), 71.49% at IC25, 98.91% at IC50, and 99.44% at IC75. Annexin V/propidium iodide (PI) flow cytometry analysis confirmed that ZnO NPs induce apoptosis in MCF-7 cells. The pro-apoptotic genes p53, p21, Bax, and JNK were upregulated, whereas anti-apoptotic genes Bcl-2, AKT1, and ERK1/2 were downregulated in a dose-dependent manner. The arrest and apoptosis of MCF-7 cells were induced by ZnO NPs through several signalling pathways.
机译:绿色产品在独特药物的发现和开发中具有强大的潜力。已经观察到氧化锌纳米颗粒(ZnO NPs)对引起乳腺癌的细胞具有强大的细胞毒性。本研究旨在检查用生物合成的ZnO NP处理的乳腺癌细胞(MCF-7)的细胞周期概况,细胞死亡状态和凋亡途径。使用MTT测定法测定ZnO NP的抗增殖活性。使用流式细胞仪评估细胞周期分析和细胞死亡模式。定量实时PCR(qRT-PCR)用于研究MCF-7细胞凋亡的表达。 ZnO NP以剂量依赖性方式对MCF-7细胞具有细胞毒性。 ZnO NPs在24小时的50%生长抑制浓度(IC50)为121 µg / mL。细胞周期分析显示,ZnO NPs诱导了G1期(凋亡),0μg/ mL(对照)时为1.87%,IC25为71.49%,IC50为98.91%,IC75为99.44%。 Annexin V /碘化丙啶(PI)流式细胞仪分析证实,ZnO NPs诱导MCF-7细胞凋亡。促凋亡基因p53,p21,Bax和JNK被上调,而抗凋亡基因Bcl-2,AKT1和ERK1 / 2被以剂量依赖的方式下调。 ZnO NPs通过多种信号途径诱导MCF-7细胞的阻滞和凋亡。

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