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用阿霉素和由提取物或芒果苷制备的金纳米颗粒共同处理Caco-2细胞可增强药物效果。

Co-Treatment of Caco-2 Cells with Doxorubicin and Gold Nanoparticles Produced from Extracts or Mangiferin Enhances Drug Effects.

作者信息

Aboyewa Jumoke A, Sibuyi Nicole R S, Goboza Mediline, Murtz Lee-Ann, Oguntibeju Oluwafemi O, Meyer Mervin

机构信息

Phytomedicine and Phytochemistry Group, Oxidative Stress Research Centre, Department of Biomedical Sciences, Cape Peninsula University of Technology, Bellville 7535, South Africa.

DSI/Mintek Nanotechnology Innovation Centre, Biolabels Node, Department of Biotechnology, University of the Western Cape, Bellville 7530, South Africa.

出版信息

Nanomaterials (Basel). 2022 Nov 7;12(21):3918. doi: 10.3390/nano12213918.

Abstract

Mangiferin (MGF) is a natural and valuable polyphenol found in significant levels in many plant species, including (). In a previous study, we synthesized gold nanoparticles (AuNPs) using MGF and a water extract of and reported that these AuNPs have very low cytotoxicity toward a human colon cancer (Caco-2) cell line. Although the study also showed that these biogenic AuNPs in combination with doxorubic (DOX) significantly augmented the cytotoxic effects of DOX in Caco-2 cells, the mechanism of the enhanced effect was not fully understood, and it was also not known if other cell lines would be sensitive to this co-treatment. In the present study, we examined the cytotoxicity of the co-treatment in Caski, HeLa, HT-29, KMST-6 and MDA-321 cell lines. Additionally, we investigated the mechanistic effects of this co-treatment in Caco-2 cells using several assays, including the adenosine triphosphate (ATP), the oxidative stress, the mitochondrial depolarization, the colony formation, the APO and the DNA fragmentation assays. We also assessed the intracellular uptake of the biogenic AuNPs. The study showed that the biogenic AuNPs were effectively taken up by the cancer cells, which, in turn, may have enhanced the sensitivity of Caco-2 cells to DOX. Moreover, the combination of the biogenic AuNPs and DOX caused a rapid depletion of ATP levels, increased mitochondrial depolarization, induced apoptosis, reduced the production of reactive oxygen species (ROS) and inhibited the long-term survival of Caco-2 cells. Although the study provided some insight into the mechanism of cytotoxicity induced by the co-treatment, further mechanistic and molecular studies are required to fully elucidate the enhanced anticancer effect of the co-treatment.

摘要

芒果苷(MGF)是一种天然且有价值的多酚,在许多植物物种中含量丰富,包括()。在先前的一项研究中,我们使用MGF和()的水提取物合成了金纳米颗粒(AuNPs),并报道这些AuNPs对人结肠癌细胞系(Caco-2)具有非常低的细胞毒性。尽管该研究还表明,这些生物合成的AuNPs与阿霉素(DOX)联合使用可显著增强DOX对Caco-2细胞的细胞毒性作用,但其增强作用的机制尚未完全了解,而且也不清楚其他细胞系是否对这种联合治疗敏感。在本研究中,我们检测了Caski、HeLa、HT-29、KMST-6和MDA-321细胞系中联合治疗的细胞毒性。此外,我们使用多种检测方法,包括三磷酸腺苷(ATP)、氧化应激、线粒体去极化、集落形成、凋亡和DNA片段化检测,研究了这种联合治疗在Caco-2细胞中的作用机制。我们还评估了生物合成的AuNPs的细胞内摄取情况。研究表明,癌细胞能够有效摄取生物合成的AuNPs,这反过来可能增强了Caco-2细胞对DOX的敏感性。此外,生物合成的AuNPs与DOX的联合使用导致ATP水平迅速耗尽,线粒体去极化增加,诱导细胞凋亡,减少活性氧(ROS)的产生,并抑制Caco-2细胞的长期存活。尽管该研究为联合治疗诱导的细胞毒性机制提供了一些见解,但仍需要进一步的机制和分子研究来充分阐明联合治疗增强的抗癌效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae80/9654788/b2da2345585f/nanomaterials-12-03918-g001.jpg

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