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姜酚白蛋白纳米粒诱导乳腺癌和结直肠癌细胞凋亡。

Carnosic Acid Encapsulated in Albumin Nanoparticles Induces Apoptosis in Breast and Colorectal Cancer Cells.

机构信息

Department of Pharmaceutical Biotechnology, College of Biotechnology, Misr University of Science and Technology, Giza 3236101, Egypt.

Department of Industrial Biotechnology, Genetic Engineering and Biotechnology Research Institute (GEBRI), University of Sadat City, Sadat City 32897, Egypt.

出版信息

Molecules. 2022 Jun 25;27(13):4102. doi: 10.3390/molecules27134102.

Abstract

Carnosic acid (CA) is a natural phenolic compound with several biomedical actions. This work was performed to study the use of CA-loaded polymeric nanoparticles to improve the antitumor activity of breast cancer cells (MCF-7) and colon cancer cells (Caco-2). CA was encapsulated in bovine serum albumin (BSA), chitosan (CH), and cellulose (CL) nanoparticles. The CA-loaded BSA nanoparticles (CA-BSA-NPs) revealed the most promising formula as it showed good loading capacity and the best release rate profile as the drug reached 80% after 10 h. The physicochemical characterization of the CA-BSA-NPs and empty carrier (BSA-NPs) was performed by the particle size distribution analysis, transmission electron microscopy (TEM), and zeta potential. The antitumor activity of the CA-BSA-NPs was evaluated by measuring cell viability, apoptosis rate, and gene expression of GCLC, COX-2, and BCL-2 in MCF-7 and Caco-2. The cytotoxicity assay (MTT) showed elevated antitumor activity of CA-BSA-NPs against MCF-7 and Caco-2 compared to free CA and BSA-NPs. Moreover, apoptosis test data showed an arrest of the Caco-2 cells at G/M (10.84%) and the MCF-7 cells at G2/M (4.73%) in the CA-BSA-NPs treatment. RT-PCR-based gene expression analysis showed an upregulation of the gene and downregulation of the BCL-2 and COX-2 genes in cells treated with CA-BSA-NPs compared to untreated cells. In conclusion, CA-BSA-NPs has been introduced as a promising formula for treating breast and colorectal cancer.

摘要

迷迭香酸(CA)是一种具有多种生物医学作用的天然酚类化合物。本研究旨在研究载 CA 的聚合物纳米粒用于提高乳腺癌细胞(MCF-7)和结肠癌细胞(Caco-2)的抗肿瘤活性。CA 被包封在牛血清白蛋白(BSA)、壳聚糖(CH)和纤维素(CL)纳米粒中。CA 负载的 BSA 纳米粒(CA-BSA-NPs)显示出最有前途的配方,因为它显示出良好的载药能力和最佳的释放率曲线,药物在 10 小时后达到 80%。CA-BSA-NPs 和空载体(BSA-NPs)的理化特性通过粒径分布分析、透射电子显微镜(TEM)和zeta 电位进行表征。通过测量 MCF-7 和 Caco-2 中的细胞活力、细胞凋亡率以及 GCLC、COX-2 和 BCL-2 的基因表达,评估 CA-BSA-NPs 的抗肿瘤活性。细胞毒性测定(MTT)显示,与游离 CA 和 BSA-NPs 相比,CA-BSA-NPs 对 MCF-7 和 Caco-2 的抗肿瘤活性更高。此外,凋亡试验数据显示,CA-BSA-NPs 处理使 Caco-2 细胞停滞在 G/M(10.84%),MCF-7 细胞停滞在 G2/M(4.73%)。基于 RT-PCR 的基因表达分析显示,与未处理细胞相比,CA-BSA-NPs 处理的细胞中 基因上调,BCL-2 和 COX-2 基因下调。总之,CA-BSA-NPs 已被引入作为治疗乳腺癌和结直肠癌的有前途的配方。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd58/9268188/650012bbe339/molecules-27-04102-g001.jpg

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