细胞凋亡
人体乳房
锌
化学
癌症研究
乳腺癌
生物
生物化学
细胞生物学
内科学
乳腺癌
医学
癌症
有机化学
作者
Wenzhen Liao,Ting Lai,Luying Chen,Junning Fu,Sreeprasad T. Sreenivasan,Zhiqiang Yu,Jiaoyan Ren
标识
DOI:10.1021/acs.jafc.5b04924
摘要
The walnut peptides and zinc ions were combined to generate a walnut peptides-zinc complex (WP1-Zn) with enhanced antiproliferative ability as well as reduced toxicity. The result indicated that Zn ions were successfully combined with WP1 through Zn–N and Zn–O covalent bonds. WP1-Zn compounds exhibited strong antiproliferative ability against the selected human cell lines, especially MCF-7 cells, whose survival rate reduced to 20.02% after exposure to 300 μg/mL of WP1-Zn for 48 h. WP1-Zn inhibited MCF-7 cell proliferation through inducing cell apoptosis and cell cycle arrest. The results indicated that WP1-Zn induced MCF-7 cell apoptosis via the ROS triggered mitochondrial-mediated pathway and cell surface receptor-mediated pathway. Our work is the first attempt to elucidate the synergic effect of novel walnut peptides and Zn and with the hope of better understanding the antiproliferative action of bioactive peptides and a zinc complex and support the potential application of WP1-Zn as a functional food ingredient or complementary medicine.
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