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负载扁柏酚的介孔硅酸钙纳米颗粒通过调节肺腺癌细胞中MDR1的功能诱导凋亡性细胞死亡。

Hinokitiol-Loaded Mesoporous Calcium Silicate Nanoparticles Induce Apoptotic Cell Death through Regulation of the Function of MDR1 in Lung Adenocarcinoma Cells.

作者信息

Shen Yu-Fang, Ho Chia-Che, Shie Ming-You, Wang Kan, Fang Hsin-Yuan

机构信息

3D Printing Medical Research Center, China Medical University Hospital, Taichung City 40447, Taiwan.

H. Milton Stewart School of Industrial and Systems Engineering, Georgia Institute of Technology, Atlanta, GA 30332, USA.

出版信息

Materials (Basel). 2016 Apr 25;9(5):306. doi: 10.3390/ma9050306.

Abstract

Hinokitiol is a tropolone-related compound found in heartwood cupressaceous plants. Hinokitiol slows the growth of a variety of cancers through inhibition of cell proliferation. The low water solubility of hinokitiol leads to less bioavailability. This has been highlighted as a major limiting factor. In this study, mesoporous calcium silicate (MCS) nanoparticles, both pure and hinokitiol-loaded, were synthesized and their effects on A549 cells were analyzed. The results indicate that Hino-MCS nanoparticles induce apoptosis in higher concentration loads (>12.5 μg/mL) for A549 cells. Hino-MCS nanoparticles suppress gene and protein expression levels of multiple drug resistance protein 1 (MDR1). In addition, both the activity and the expression levels of caspase-3/-9 were measured in Hino-MCS nanoparticle-treated A549 cells. The Hino-MCS nanoparticles-triggered apoptosis was blocked by inhibitors of pan-caspase, caspase-3/-9, and antioxidant agents (N-acetylcysteine; NAC). The Hino-MCS nanoparticles enhance reactive oxygen species production and the protein expression levels of caspase-3/-9. Our data suggest that Hino-MCS nanoparticles trigger an intrinsic apoptotic pathway through regulating the function of MDR1 and the production of reactive oxygen species in A549 cells. Therefore, we believe that Hino-MCS nanoparticles may be efficacious in the treatment of drug-resistant human lung cancer in the future.

摘要

扁柏酚是一种在柏科植物心材中发现的与托酚酮相关的化合物。扁柏酚通过抑制细胞增殖来减缓多种癌症的生长。扁柏酚的低水溶性导致其生物利用度较低。这已被视为一个主要限制因素。在本研究中,合成了纯的和负载扁柏酚的介孔硅酸钙(MCS)纳米颗粒,并分析了它们对A549细胞的影响。结果表明,对于A549细胞,负载扁柏酚的MCS纳米颗粒(Hino-MCS纳米颗粒)在较高浓度负载(>12.5μg/mL)时可诱导细胞凋亡。Hino-MCS纳米颗粒可抑制多药耐药蛋白1(MDR1)的基因和蛋白表达水平。此外,还检测了经Hino-MCS纳米颗粒处理的A549细胞中半胱天冬酶-3/-9的活性和表达水平。泛半胱天冬酶、半胱天冬酶-3/-9的抑制剂以及抗氧化剂(N-乙酰半胱氨酸;NAC)可阻断Hino-MCS纳米颗粒引发的细胞凋亡。Hino-MCS纳米颗粒可增强活性氧的产生以及半胱天冬酶-3/-9的蛋白表达水平。我们的数据表明,Hino-MCS纳米颗粒通过调节A549细胞中MDR1的功能和活性氧的产生来触发内源性凋亡途径。因此,我们认为Hino-MCS纳米颗粒未来可能对耐药性人类肺癌的治疗有效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5566/5503060/1da9fcfdecae/materials-09-00306-g001.jpg

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