Novel peptides derived from S. hispanica seeds induce selective cytotoxicity on human cancer cells

被引:1
作者
Bojorquez, Nidia del Carmen Quintal [1 ]
Campos, Maira Rubi Segura [1 ]
机构
[1] Univ Autonoma Yucatan, Fac Ingn Quim, Periferico Norte Km 33-5, Merida 13615, Yucatan, Mexico
关键词
Anticancer peptides; Cytotoxicity; Bioactive compounds; Anticancer therapy; Nutraceuticals; ANTICANCER ACTIVITY; APOPTOSIS; DEATH; CASPASES; SIDE;
D O I
10.1016/j.foodchem.2024.140470
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Cancer prevails as one of the major health concerns worldwide due to the consistent rise in incidence and lack of effective therapies. Previous studies identified the peptides KLKKNL, MLKSKR, and KKYRVF from Salvia hispanica seeds and stated their selective anticancer activity. Thus, this study aimed to determine the cell death pathway induced by these peptides on five cancer cell lines (MCF-7, Caco2, HepG2, DU145, and HeLa). Based on the results of this work, it is possible to suggest that KLKKNL primarily induces selective cancer cell death through the apoptotic pathway in the Caco2 and HeLa lines. On the other hand, the peptide KKYRVF reported the highest statistical (p p < 0.05) selective cytotoxic effect on the MCF-7, Caco2, HepG2, and DU145 cancer cell lines by induction of the necrotic pathway. These findings offer some understanding of the selective anticancer effect of KLKKNL, MLKSKR, and KKYRVF.
引用
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页数:13
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