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新型鞣花酸和安石榴苷纳米原型物通过 ROS 介导的细胞凋亡诱导乳腺癌细胞毒性。

Newly Synthesized Punicalin and Punicalagin Nano-Prototypes Induce Breast Cancer Cytotoxicity Through ROS-Mediated Apoptosis.

机构信息

Department of Hormones, Medical Research and Clinical Studies Institute, National Research Center, Dokki 12622, Giza, Egypt.

出版信息

Asian Pac J Cancer Prev. 2022 Jan 1;23(1):363-376. doi: 10.31557/APJCP.2022.23.1.363.

Abstract

OBJECTIVE

Globally, breast cancer represents serious cause of morbidity and mortality. Our goal is to improve nutraceuticals that have the ability to overlap the side effects of conventional therapies and promising tumoricidal effects by using nanotechnology techniques. The current work was premeditated to explore the apoptotic effects of punicalin (PN) and punicalagin (PNG) nano-prototypes, derived from Punica granatum, on human breast cancerous MCF7 and MDA-MB-231 cells in vitro.

METHODS

Firstly, we prepared and characterized of PN, PGN, and 5-flurouracil (FU)-loaded PLGA, PLGA-coated-CS, and PLGA-coated-CS-PEG nano-prototypes. Then, we studied the toxicological and biochemical effects of all nanoformulations. Finally, we measured the genetic and protein expression levels of apoptotic and survival candidates in cancer cells.

RESULTS

Our results showed that the newly synthesized nano-prototypes had cytotoxic and apoptotic effects on MCF7 and MDA-MB-231 cell lines. Moreover, they up-regulated Bax and Cas-3 expression levels, as well as down-regulated BCL-2, NF-ĸB and PI3k expression levels compared to control. Nitric oxide (NO) and zinc (Zn) levels were significantly elevated (P < 0.05) after the application of PN and PNG nano-prototypes compared to the control.

CONCLUSION

PN and PNG nano-prototypes of PLGA decorated with CS and PEG enhanced the anti-cancer activity through induction of cytotoxicity, reactive oxygen species (ROS)-mediated apoptosis.

摘要

目的

在全球范围内,乳腺癌是导致发病率和死亡率的主要原因。我们的目标是利用纳米技术改善具有减轻常规疗法副作用和有前途的杀肿瘤作用的营养药物。目前的工作旨在探索从石榴中提取的 punicalin (PN) 和 punicalagin (PNG) 纳米原型对体外人乳腺癌 MCF7 和 MDA-MB-231 细胞的凋亡作用。

方法

首先,我们制备和表征了 PN、PGN 和负载 5-氟尿嘧啶 (FU) 的 PLGA、PLGA 涂层 CS 和 PLGA 涂层 CS-PEG 纳米原型。然后,我们研究了所有纳米制剂的毒理学和生化效应。最后,我们测量了癌细胞中凋亡和存活候选基因的遗传和蛋白表达水平。

结果

我们的结果表明,新合成的纳米原型对 MCF7 和 MDA-MB-231 细胞系具有细胞毒性和凋亡作用。此外,与对照组相比,它们上调了 Bax 和 Cas-3 的表达水平,同时下调了 BCL-2、NF-ĸB 和 PI3k 的表达水平。与对照组相比,PN 和 PNG 纳米原型应用后,一氧化氮 (NO) 和锌 (Zn) 水平显著升高 (P < 0.05)。

结论

PLGA 修饰的 CS 和 PEG 上的 PN 和 PNG 纳米原型通过诱导细胞毒性、活性氧 (ROS) 介导的凋亡增强了抗癌活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3242/9258674/36f0d4afb3aa/APJCP-23-363-g001.jpg

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