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所选不对称双吖啶类化合物对 HCT116 结肠和 A549 肺癌多细胞肿瘤球与单层培养物的细胞效应比较。

Cellular Effects of Selected Unsymmetrical Bisacridines on the Multicellular Tumor Spheroids of HCT116 Colon and A549 Lung Cancer Cells in Comparison to Monolayer Cultures.

机构信息

Department of Pharmaceutical Technology and Biochemistry, Faculty of Chemistry, Gdańsk University of Technology, 80-233 Gdańsk, Poland.

出版信息

Int J Mol Sci. 2023 Oct 30;24(21):15780. doi: 10.3390/ijms242115780.

Abstract

Multicellular tumor spheroids are a good tool for testing new anticancer drugs, including those that may target cancer stem cells (CSCs), which are responsible for cancer progression, metastasis, and recurrence. Therefore, we applied this model in our studies of highly active antitumor unsymmetrical bisacridines (UAs). We investigated the cellular response induced by UAs in 2D and 3D cultures of HCT116 colon and A549 lung cancer cells, with an additional focus on their impact on the CSC-like population. We showed that UAs affected the viability of the studied cells, as well as their spherogenic potential in the 2D and 3D cultures. Furthermore, we proved that the most promising UAs (C-2045 and C-2053) induced apoptosis in the HCT116 and A549 spheres to a similar, or even higher, extent than what was found in monolayer conditions. Next, we identified the population of the CSC-like cells in the 2D and 3D cultures of the studied cell lines by determining the levels of CD166, CD133, CD44, and EpCAM markers. We showed that the selected UAs affected the CSC-like population in both of the cell lines, and that A549 was affected more profoundly in 3D than in 2D cultures. Thus, the UAs exhibited high antitumor properties in both the 2D and 3D conditions, which makes them promising candidates for future therapeutic applications.

摘要

多细胞肿瘤球体是测试新抗癌药物的良好工具,包括那些可能针对癌症干细胞(CSC)的药物,CSC 负责癌症的进展、转移和复发。因此,我们在对高活性非对称双吖啶(UA)的研究中应用了这种模型。我们研究了 UA 在 HCT116 结肠和 A549 肺癌细胞的 2D 和 3D 培养物中诱导的细胞反应,特别关注它们对 CSC 样细胞群的影响。我们表明,UA 影响了研究细胞的活力,以及它们在 2D 和 3D 培养物中的成球能力。此外,我们证明了最有前途的 UA(C-2045 和 C-2053)在 HCT116 和 A549 球体中诱导凋亡的程度与在单层条件下相似,甚至更高。接下来,我们通过确定 CD166、CD133、CD44 和 EpCAM 标记物的水平,确定了研究细胞系的 2D 和 3D 培养物中的 CSC 样细胞群。我们表明,所选 UA 影响了两种细胞系中的 CSC 样细胞群,并且 A549 在 3D 培养物中比在 2D 培养物中受影响更大。因此,UA 在 2D 和 3D 条件下均表现出高抗肿瘤特性,使其成为未来治疗应用的有前途的候选药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88b7/10649579/b1919b2b298e/ijms-24-15780-g001.jpg

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