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Anticancer property of Hemp Bioactive Peptides in Hep3B liver cancer cells through Akt/GSK3β/β‐catenin signaling pathway

机译:HEP3B肝癌细胞HEP3B生物活性肽的抗癌性能通过AKT /GSK3β/β-catenin信号通路

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摘要

Foodborne protein hydrolysates exhibit biological activity that may be therapeutic in a number of human disease settings. Hemp peptides (HP) generated by controlled hydrolysis of hemp proteins have a number of health benefits and are of pharmaceutical value. In the present study, we produce small molecular weight HP from hemp seed and investigate its anticancer properties in Hep3B human liver cancer cells. We demonstrate that HP treatment increased apoptosis, reduced cell viability, and reduced cell migration in Hep3B human liver cancer cells without affecting the normal liver cell line L02. We correlate these phenotypes with increased cellular ROS levels, upregulation of cleaved caspase 3 and Bad, and downregulation of antiapoptotic Bcl‐2. HP treatment led to increased Akt and GSK‐3β phosphorylation, with subsequent downregulation of β‐catenin, suggesting β‐catenin signaling modulation as a critical mechanism by which HP exhibits anticancer properties. Our findings suggest HP are of potential therapeutic interest for liver cancer treatment.
机译:食源性蛋白质水解产物表现出可能在许多人类疾病环境中治疗的生物活性。受约束水解产生的Hemp肽(HP)具有多种健康益处,具有药物价值。在本研究中,我们从大麻种子生产小分子量HP,并在Hep3B人肝癌细胞中探讨其抗癌性质。我们证明HP治疗增加了凋亡,降低细胞活力,降低了Hep3B人肝癌细胞中的细胞迁移,而不影响正常的肝细胞系L02。我们将这些表型与增加的细胞ROS水平相关,裂解的胱天蛋白酶3的上调和良好的抗凋亡Bcl-2的下调。 HP处理导致AKT和GSK-3β磷酸化增加,随后的β-连环蛋白下调,表明β-连环蛋白信号调制作为关键机制,通过该机制,HP表现出抗癌性质。我们的研究结果表明HP对肝癌治疗有潜在的治疗兴趣。

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