Dilloo Silvia, Whittaker Anne, Chang Xinyue, D'Amen Eros, Spisni Enzo, Hrelia Silvana, Angeloni Cristina, Malaguti Marco, Dinelli Giovanni, Truzzi Francesca
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.
Int J Mol Sci. 2024 Dec 13;25(24):13362. doi: 10.3390/ijms252413362.
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.
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。