Genistein-Aspirin Combination Exerts Cytotoxic and Anti-Migratory Effects in Human Colorectal Cancer Cells

被引:2
作者
Iftode, Claudia [1 ]
Iurciuc, Stela [1 ]
Marcovici, Iasmina [2 ,3 ]
Macasoi, Ioana [2 ,3 ]
Coricovac, Dorina [2 ,3 ]
Dehelean, Cristina [2 ,3 ]
Ursoniu, Sorin [1 ,4 ]
Rusu, Andreea [5 ]
Ardelean, Simona [5 ]
机构
[1] Victor Babes Univ Med & Pharm Timisoara, Fac Med, Eftimie Murgu Sq 2, Timisoara 300041, Romania
[2] Victor Babes Univ Med & Pharm Timisoara, Fac Pharm, Eftimie Murgu Sq 2, Timisoara 300041, Romania
[3] Victor Babes Univ Med & Pharm Timisoara, Fac Pharm, Res Ctr Pharmacotoxicol Evaluat, Eftimie Murgu Sq 2, Timisoara 300041, Romania
[4] Victor Babes Univ Med & Pharm Timisoara, Ctr Translat Res & Syst Med, Eftimie Murgu Sq 2, Timisoara 300041, Romania
[5] Vasile Goldis Western Univ Arad, Fac Pharm, Revolutiei Bvd 94, Arad 310130, Romania
来源
LIFE-BASEL | 2024年 / 14卷 / 05期
关键词
genistein; aspirin; colorectal cancer; cytotoxicity; angiogenesis; chemoprevention; migration; SYNERGISTIC ANTITUMOR-ACTIVITY; ANGIOGENESIS; METASTASIS; ACTIVATION; APOPTOSIS; INVASION; TARGETS; GROWTH; AKT;
D O I
10.3390/life14050606
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Colorectal cancer (CRC) is a heterogenous pathology with high incidence and mortality rates globally, but it is also preventable so finding the most promising candidates (natural compounds or repurposed drugs) to be chemopreventive alternatives has become a topic of interest in recent years. The present work aims to elucidate the potential effects of a combination between genistein (GEN), an isoflavone of natural origin, and aspirin (ASA) in CRC prevention/treatment by performing an in vitro evaluation in human colorectal cancer cells (HCT-116) and an in ovo analysis using the chick embryo chorioallantoic membrane (CAM) model. Cell viability was verified by an MTT (migratory potential by scratch) assay, and the expressions of MMP-2 and MMP-9 were analyzed using RT-qPCR. Our results indicated a dose-dependent cytotoxic effect of ASA (2.5 mM) + GEN (10-75 mu M) combination characterized by reduced cell viability and morphological changes (actin skeleton reorganization and nuclei deterioration), an inhibition of HCT-116 cells' migratory potential by down-regulating MMP-2 and MMP-9 mRNA expressions, and an antiangiogenic effect by modifying the vascular network. These promising results raise the possibility of future in-depth investigations regarding the chemopreventive/therapeutical potential of ASA+GEN combination.
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页数:21
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