Micucci Matteo, Battistelli Michela, Burattini Sabrina, Mari Michele, Retini Michele, Osman Riham, Versari Ilaria, Stella Anna Bartoletti, Gianfanti Federico, Udodinma Jude Okeke, Onesimo Francesco, Riela Serena, Canale Matteo, Piccionello Antonio Palumbo, Faenza Irene, Salucci Sara
Department of Biomolecular Sciences University of Urbino Carlo Bo Urbino Italy.
Department of Biomedical and NeuroMotor Sciences University of Bologna Bologna Italy.
Food Sci Nutr. 2025 May 30;13(6):e70350. doi: 10.1002/fsn3.70350. eCollection 2025 Jun.
This study investigates the chemopreventive potential of a grape pomace extract (GPE) derived from Verdicchio grapes, aligning with circular economy principles to repurpose winery waste into a nutraceutical targeting gastric cancer prevention. Soxhlet extraction yielded a bioactive-rich extract. Comprehensive chemical characterization via HPLC/ESI/Q-TOF identified 39 metabolites spanning key chemical classes. Anthocyanins were predominant, with malvidin glucoside (12,546 mg/kg DM; 36.3%), malvidin coumaroyl glucoside (9941 mg/kg DM; 28.8%), and malvidin acetylglucoside (7189 mg/kg DM; 20.8%) as the most abundant compounds. Carboxylic acids included tartaric, malic, isocitric, aconitic, and succinic acids, while lipid molecules, such as phytosphingosine and stearic acid, and amino acids like proline, valine, leucine, and phenylalanine further enriched the extract's chemical heterogeneity. Biological evaluations revealed GPE's selective cytotoxicity against AGS (IC: 13.64 μg/mL) and KATO III (IC: 7.11 μg/mL) gastric cancer cells, sparing GES-1 cells. Mechanistically, GPE-induced apoptosis through caspase-3 activation and mitochondrial dysfunction, as evidenced by inner membrane disruption and cardiolipin peroxidation. TEM and CLSM morphological analyses revealed hallmark apoptotic features, including chromatin condensation, micronuclei formation, and apoptotic bodies. Additionally, GPE impaired autophagy, marked by Beclin-1 downregulation and LC3B-II upregulation. The accumulation of degradative vacuoles indicated disrupted autophagosome clearance, shifting autophagy from a survival mechanism to a cell death-promoting pathway. These findings highlight GPE's dual impact on apoptosis and autophagy in gastric cancer cells, underscoring its potential as a dietary intervention for gastric cancer prevention.
本研究调查了源自韦迪奇奥葡萄的葡萄渣提取物(GPE)的化学预防潜力,这符合循环经济原则,即将酿酒厂废料重新利用,制成一种针对预防胃癌的营养保健品。索氏提取法得到了一种富含生物活性成分的提取物。通过HPLC/ESI/Q-TOF进行的综合化学表征鉴定出39种代谢物,涵盖关键化学类别。花青素占主导地位,其中矢车菊素葡萄糖苷(12,546毫克/千克干物质;36.3%)、矢车菊素香豆酰葡萄糖苷(9941毫克/千克干物质;28.8%)和矢车菊素乙酰葡萄糖苷(7189毫克/千克干物质;20.8%)是含量最丰富的化合物。羧酸包括酒石酸、苹果酸、异柠檬酸、乌头酸和琥珀酸,而脂质分子,如植物鞘氨醇和硬脂酸,以及氨基酸如脯氨酸、缬氨酸、亮氨酸和苯丙氨酸进一步丰富了提取物的化学异质性。生物学评估显示,GPE对AGS(IC:13.64微克/毫升)和KATO III(IC:7.11微克/毫升)胃癌细胞具有选择性细胞毒性,而对GES-1细胞无毒性。从机制上讲,GPE通过激活caspase-3和线粒体功能障碍诱导细胞凋亡,内膜破坏和心磷脂过氧化证明了这一点。透射电子显微镜(TEM)和共聚焦激光扫描显微镜(CLSM)形态分析揭示了典型的凋亡特征,包括染色质浓缩、微核形成和凋亡小体。此外,GPE损害自噬,表现为Beclin-1下调和LC3B-II上调。降解性液泡的积累表明自噬体清除受阻,使自噬从一种生存机制转变为促进细胞死亡的途径。这些发现突出了GPE对胃癌细胞凋亡和自噬的双重影响,强调了其作为预防胃癌的饮食干预措施的潜力。