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聚合物纳米颗粒共递送姜黄素和白杨素协同抑制人结肠癌细胞的生长和hTERT基因表达。

Co-Delivery of Curcumin and Chrysin by Polymeric Nanoparticles Inhibit Synergistically Growth and hTERT Gene Expression in Human Colorectal Cancer Cells.

作者信息

Lotfi-Attari Javid, Pilehvar-Soltanahmadi Younes, Dadashpour Mehdi, Alipour Shahriar, Farajzadeh Raana, Javidfar Shahrzad, Zarghami Nosratollah

机构信息

a Department of Medical Biotechnology, Faculty of Advanced Medical Sciences , Tabriz University of Medical Sciences , Tabriz , Iran.

b Department of Molecular Medicine, Faculty of Advanced Medical Sciences , Tabriz University of Medical Sciences , Tabriz , Iran.

出版信息

Nutr Cancer. 2017 Nov-Dec;69(8):1290-1299. doi: 10.1080/01635581.2017.1367932. Epub 2017 Oct 30.

Abstract

Nanoparticle (NP)-based combinational chemotherapy has been proposed as a potent approach for improving intracellular drug concentrations and attaining synergistic effects in colorectal cancer therapy. Here, two well-known herbal substances, Curcumin (Cur) and Chrysin (Chr), were co-encapsulated in PEGylated PLGA NPs and investigated their synergistic inhibitory effect against Caco-2 cancer cells. Characterization of nanoformulated drugs was determined using DLS, FTIR, TEM, and SEM. Drug release study was performed using dialysis method. MTT and real-time PCR assays were applied to evaluate the cytotoxic effects of free and nano-encapsulated drugs on expression level of hTERT in Caco-2 cells. The results showed that free drugs and nano-formulations exhibited a dose-dependent cytotoxicity against Caco-2 cells and especially, Cur-Chr-PLGA/PEG NPs had more synergistic antiproliferative effect and significantly arrested the growth of cancer cells than the other groups (P < 0.05). Real-time PCR results revealed that Cur, Chr, and combination of Cur-Chr in free and encapsulated forms inhibited hTERT gene expression. Also, it was found that Cur-Chr-PLGA/PEG NPs than free combination forms could further decline hTERT expression in all concentration (P < 0.05). In summary, our study represents the first report of nano-combinational application of the natural herbal substances with a one-step fabricated codelivery system for effective colorectal cancer combinational chemotherapy.

摘要

基于纳米颗粒(NP)的联合化疗已被认为是提高细胞内药物浓度并在结直肠癌治疗中获得协同效应的有效方法。在此,两种著名的草药成分姜黄素(Cur)和白杨素(Chr)被共包封于聚乙二醇化聚乳酸-羟基乙酸共聚物纳米粒(PEGylated PLGA NPs)中,并研究了它们对Caco-2癌细胞的协同抑制作用。采用动态光散射(DLS)、傅里叶变换红外光谱(FTIR)、透射电子显微镜(TEM)和扫描电子显微镜(SEM)对纳米制剂药物进行表征。采用透析法进行药物释放研究。应用MTT法和实时聚合酶链反应(PCR)分析评估游离和纳米包封药物对Caco-2细胞中人类端粒酶逆转录酶(hTERT)表达水平的细胞毒性作用。结果表明,游离药物和纳米制剂对Caco-2细胞均表现出剂量依赖性细胞毒性,尤其是Cur-Chr-PLGA/PEG纳米粒比其他组具有更强的协同抗增殖作用,能显著抑制癌细胞生长(P<0.05)。实时PCR结果显示,游离和包封形式的Cur、Chr以及Cur-Chr组合均抑制hTERT基因表达。此外,还发现Cur-Chr-PLGA/PEG纳米粒在所有浓度下比游离组合形式能进一步降低hTERT表达(P<0.05)。总之,我们的研究首次报道了天然草药成分通过一步制备的共递送系统进行纳米联合应用,用于有效的结直肠癌联合化疗。

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