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微生物 β-葡萄糖醛酸苷酶水凝胶珠激活化学治疗前药。

Microbial β-Glucuronidase Hydrogel Beads Activate Chemotherapeutic Prodrug.

机构信息

Department of Bioengineering, University of Illinois at Urbana-Champaign, Urbana, Illinois 60801, United States.

Cancer Center at Illinois, Carle-Illinois College of Medicine, University of Illinois at Urbana-Champaign, Urbana, Illinois 60801, United States.

出版信息

ACS Appl Mater Interfaces. 2024 Jun 5;16(22):28093-28103. doi: 10.1021/acsami.4c02568. Epub 2024 May 22.

Abstract

Bacteria-assisted chemotherapeutics have been highlighted as an alternative or supplementary approach to treating cancer. However, dynamic cancer-microbe studies at the level have remained a challenge to show the impact and effectiveness of microbial therapeutics due to the lack of relevant coculture models. Here, we demonstrate a hydrogel-based compartmentalized system for prodrug activation of a natural ingredient of licorice root, glycyrrhizin, by microbial β-glucuronidase (GUS). Hydrogel containment with provides a favorable niche to encode GUS enzymes with excellent permeability and can serve as an independent ecosystem in the transformation of pro-apoptotic materials. Based on the confinement system of GUS expressing microbes, we quantitatively evaluated chemotherapeutic effects enhanced by microbial GUS enzyme in two dynamic coculture models (i.e., 2D monolayered cancer cells and 3D tumor spheroids). Our findings support the processes of prodrug conversion mediated by bacterial GUS enzyme which can enhance the therapeutic efficacy of a chemotherapy drug under dynamic coculture conditions. We expect our coculture platforms can be used for the evaluation of pharmacological properties and biological activity of xenobiotics as well as the potential impact of microbes on cancer therapeutics.

摘要

细菌辅助化疗已被强调为治疗癌症的一种替代或补充方法。然而,由于缺乏相关的共培养模型,在水平上进行动态的癌症-微生物研究一直是展示微生物治疗效果和有效性的挑战。在这里,我们展示了一种基于水凝胶的分隔系统,用于通过微生物β-葡萄糖醛酸酶(GUS)激活甘草根的天然成分甘草酸的前药。用提供水凝胶容纳物,为编码具有优异渗透性的 GUS 酶提供了有利的小生境,并可以作为转化促凋亡物质的独立生态系统。基于表达 GUS 的微生物的封闭系统,我们在两种动态共培养模型中定量评估了微生物 GUS 酶增强的化疗效果(即 2D 单层癌细胞和 3D 肿瘤球体)。我们的研究结果支持细菌 GUS 酶介导的前药转化过程,该过程可以增强化疗药物在动态共培养条件下的治疗效果。我们期望我们的共培养平台可用于评估外源性物质的药理学特性和生物活性以及微生物对癌症治疗的潜在影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b35/11164065/9c3ab7d9014b/am4c02568_0001.jpg

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