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施用亚精胺和丁香酚对转移性SW620和原发性Caco-2结肠直肠癌球体显示出抗肿瘤功效。

Administration of Spermidine and Eugenol Demonstrates Anti-Tumorigenic Efficacy on Metastatic SW620 and Primary Caco-2 Colorectal Cancer Spheroids.

作者信息

Dilloo Silvia, Whittaker Anne, Chang Xinyue, D'Amen Eros, Spisni Enzo, Hrelia Silvana, Angeloni Cristina, Malaguti Marco, Dinelli Giovanni, Truzzi Francesca

机构信息

Department of Agricultural and Food Sciences, Alma Mater Studiorum-University of Bologna, 40127 Bologna, Italy.

Department of Biological, Geological, and Environmental Sciences, Alma Mater Studiorum-University of Bologna, 40127 Bologna, Italy.

出版信息

Int J Mol Sci. 2024 Dec 13;25(24):13362. doi: 10.3390/ijms252413362.

DOI:10.3390/ijms252413362
PMID:39769127
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11679521/
Abstract

The anti-cancer potential of eugenol (EUG) is well recognized, whereas that of spermidine (SPD) is subject to dispute and requires further research. The anti-tumorigenic potential of wheat germ SPD (150 µM) and clove EUG (100 µM), alone, in combination as SPD+EUG (50 µM + 100 µM) and, as a supplement (SUPPL; 0.6 µM SPD + 50 µM EUG), was investigated on both metastatic SW620 and primary Caco-2 colorectal cancer (CRC) spheroids. Compared to untreated controls, all treatments significantly reduced the vitality and spheroid area, increased the necrotic area, and induced apoptosis on both cell-type spheroids after 96 h, with a reduced migration evident in 2D (two-dimensional) cultures after 48 h. The comparable anti-CRC effects of the SPD+EUG and the SUPPL reflected a wide-range dose efficacy of SPD and EUG. It is of note that SPD+EUG induced a synergistic effect on the increased caspase-3 expression and reduced the migration percentage in SW620. In more physiologically relevant intestinal equivalents (healthy enterocytes [NCM460], fibroblasts [L929], and monocytes [U937]) containing embedded SW620/Caco-2 spheroids, SPD+EUG administration significantly reduced the spheroid CEA marker and proliferation, whilst simultaneously increasing occludin, autophagy LC3-II expression, and monocyte differentiation, compared to the control models. Exogenous SPD, alone and in combination with EUG, displayed an anti-CRC potential on tumor growth and metastasis, and warrants further investigation.

摘要

丁香酚(EUG)的抗癌潜力已得到广泛认可,而亚精胺(SPD)的抗癌潜力仍存在争议,需要进一步研究。分别研究了小麦胚芽SPD(150µM)和丁香EUG(100µM)单独使用、联合使用(SPD+EUG,50µM+100µM)以及作为补充剂(SUPPL;0.6µM SPD+50µM EUG)对转移性SW620和原发性Caco-2结直肠癌(CRC)球体的抗肿瘤潜力。与未处理的对照相比,所有处理在96小时后均显著降低了两种细胞类型球体的活力和球体面积,增加了坏死面积,并诱导了细胞凋亡,在48小时后的二维(2D)培养中迁移明显减少。SPD+EUG和SUPPL具有相当的抗CRC作用,反映了SPD和EUG的广泛剂量效应。值得注意的是,SPD+EUG对SW620中caspase-3表达的增加具有协同作用,并降低了迁移百分比。在含有嵌入SW620/Caco-2球体的更具生理相关性的肠道等效物(健康肠上皮细胞[NCM460]、成纤维细胞[L929]和单核细胞[U937])中,与对照模型相比,给予SPD+EUG可显著降低球体CEA标志物和增殖,同时增加闭合蛋白、自噬LC3-II表达和单核细胞分化。外源性SPD单独或与EUG联合使用,对肿瘤生长和转移显示出抗CRC潜力,值得进一步研究。

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