冷杉介导的银纳米颗粒抑制乳腺癌MCF-7细胞生长并促进细胞凋亡。

Guanghui Ren, Xiaoyan Hao, Shuyi Yan, Jun Chen, Guobin Qiu, K. Ang, Mohd Islahuddin Mohd Tamrin
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引用次数: 2

摘要

由于乳腺上皮组织中肿瘤细胞不受控制的增殖,乳腺癌是全世界妇女死亡的第二大原因。银纳米颗粒由冷杉叶片(AS-AgNPs)配制而成,并通过紫外可见光谱、FTIR、SEM和XRD等多种方法进行了表征。分析了制备的AS-AgNPs对MCF-7细胞的体外抗癌潜力。MTT试验研究了制备的AS-AgNPs对MCF-7细胞的细胞毒性。采用荧光染色技术研究AS-AgNPs补充后MCF-7细胞中ROS积累量和MMP水平。用检测试剂盒检测Caspase活性。采用标准方法检测氧化应激和抗氧化生物标志物(TBARS、SOD、CAT和GSH)水平。采用RT-PCR法检测AS-AgNPs给药MCF-7细胞中凋亡标志物Bax、Bcl-2的表达。MTT实验结果表明,提取液和制备的AS-AgNPs均能显著降低MCF-7细胞的凋亡。然而,植物提取物和AS-AgNPs均未影响MCF-10A细胞的细胞活力。此外,制备的AS-AgNPs改善了MCF-7细胞中的ROS积累,并减少了MMP状态。给予AS-AgNPs的MCF-7细胞显示出TBARS含量的提高和抗氧化剂的减少。AS-AgNPs显著提高了MCF-7细胞中caspase-9和-3活性以及Bax的表达,降低了Bcl-2的表达。因此,目前的研究报告表明,配方AS-AgNPs通过增加ROS、氧化应激和凋亡蛋白表达,在体外对MCF-7细胞表现出显著的抗癌作用。制备的AS-AgNPs在未来可能成为一种抗癌药物。
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Abies spectabilis-Mediated Silver Nanoparticles Inhibits Cell Growth and Promotes Apoptosis in Breast Cancer MCF-7 Cells.
Breast cancer is the second most cause of mortality among women worldwide due to the uncontrolled proliferation of tumor cells in the mammary epithelial tissues. The silver nanoparticles were formulated from the Abies spectabilis leaf (AS-AgNPs) and characterized by various practices like UV-vis spectroscopy, FTIR, SEM, and XRD. The in vitro anticancer potential of fabricated AS-AgNPs against the MCF-7 cells were analyzed. The MTT test was executed to investigate the cytotoxic nature of fabricated AS-AgNPs against MCF-7 cells. The magnitudes of ROS accumulation and MMP level in the AS-AgNPs supplemented MCF-7 cells were studied using fluorescent staining techniques. Caspase activities were studied using assay kits. The contents of oxidative stress and antioxidant biomarker (TBARS, SOD, CAT, and GSH) levels were scrutinized by standard methods. The expressions of apoptotic markers like Bax and Bcl-2 in the AS-AgNPs administered MCF-7 cells were detected by RT-PCR assay. The MTT findings showed that both extract and fabricated AS-AgNPs remarkably decreased the MCF-7 cells. Nonetheless, both plant extract and AS-AgNPs did not affect the cell viability of MCF-10A cells. Furthermore, the fabricated AS-AgNPs improved the ROS accumulation, and depleted the MMP status in the MCF-7 cells. AS-AgNPs administered MCF-7 cells demonstrated the improved TBARS content and depleted antioxidants. The treatment with AS-AgNPs considerably elevated the caspase-9 and -3 activities and Bax expression, while decreasing the Bcl-2 expression in MCF-7 cells. Hence the current investigation reports that the formulated AS-AgNPs exhibited remarkable in vitro anticancer action against MCF-7 cells through increased ROS, oxidative stress, and apoptotic protein expression. The fabricated AS-AgNPs could be a possible anticancer remedy in the future.
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