Colon cancer is one of the most common malignant tumors worldwide and is associated with high morbidity and mortality. Conventional treatments are typically administered at advanced stages and often lead to severe adverse effects. Therefore, developing safe and effective nutritional interventions from natural food sources is of great importance for the prevention and management of colon cancer. Dairy-derived protein hydrolysates have received increasing attention as functional food components due to their biological activities and favorable safety profiles. In this study, lactoferrin (LF) was hydrolyzed using alkaline protease to obtain lactoferrin hydrolysate (LFH). LFH was administered to mice with azoxymethane/dextran sulfate sodium-induced colon cancer to evaluate its protective effects. LFH markedly alleviated colonic tissue injury, reduced serum levels of pro-inflammatory cytokines IL-1β, IL-6, and TNF-α, and decreased the expression of tumor markers CEA, CA19-9, as well as the proliferation marker Ki-67, thereby inhibiting tumor progression. At the molecular level, LFH downregulated key genes in the Wnt/β-catenin pathway, including c-Myc, β-catenin, and Cyclin D1. Furthermore, LFH upregulated pro-apoptotic genes Bax, caspase-9, caspase-3, and p53, while downregulating anti-apoptotic genes Bcl-2 and Bcl-xl, suggesting enhanced apoptotic responses in tumor cells. LFH also significantly improved gut microbiota composition by reducing harmful bacteria such as Bacillus, Enterorhabdus, and Odoribacter, while increasing beneficial genera including Ruminococcus and Eubacterium_siraeum_group. Correspondingly, LFH elevated several gut microbial metabolites such as Chrysogine, Agmatine, 5′-Deoxy-5-Fluorocytidine, and Glutamyl-γ-Glutamate. Overall, this study provides new insights into the biological effects of LFH on colon cancer and supports its potential application in the development of LFH-based functional foods.
Han-Jun Jiang, Xue Deng, Jing Yang et al.· Food Science and Human Welln...· 0 citations
This study investigates how electrostatic interactions between whey protein isolate (WPI) and polysaccharides (konjac glucomannan, guar gum, pectin, sodium alginate, chitosan) affect the stability and encapsulation of high-internal-phase emulsions (HIPEs, oil fraction >74%), revealing charge-driven structural and network stabilization mechanisms. The findings demonstrate that anionic WPI (pH 7.0) alone was more effective than cationic WPI (pH 4.0) in stabilizing oil-in-water HIPEs. Neutral polysaccharides enhanced emulsifying performance through viscosity-induced stabilization. While electrostatic repulsion increased ζ-potential of the complexes, thereby synergistically strengthening hydrophobic interaction-driven emulsifying activity. In contrast, excessive attraction (pectin, ζ-potential -17.0 mV) destabilized structural network through bridging or depletion flocculation, whereas moderate attraction (sodium alginate, ζ-potential -11.5 mV), facilitated the formation of stable emulsion systems. Notably, sodium alginate-WPI systems demonstrated robust stability (for 4 months) across all electrostatic conditions and offered excellent biocompatibility (<5%) and probiotic protection (>9.05 log CFU/mL). Collectively, these findings elucidate the mechanism of electrostatic tuning in stabilization of HIPEs, providing a promising approach for probiotics delivery.