基于Correa级联的天然产物治疗胃癌三部曲:现状与未来展望

Journal of pharmaceutical analysis Pub Date : 2025-02-01 Epub Date: 2024-08-19 DOI:10.1016/j.jpha.2024.101075
Wenhao Liao, Jing Wang, Yuchen Li
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引用次数: 0

摘要

胃癌是一种多因子参与、多细胞调控、多阶段发展的恶性肿瘤。经典的Correa肠GC级联描述了胃粘膜恶性转化的三部曲,正常胃粘膜从非活动性或慢性活动性胃炎(I期)到胃癌前病变(II期),最后到胃癌(III期)。Correa级联强调了胃癌的进化模式和早期干预预防胃粘膜恶性转化的重要性。干预早期胃粘膜病变,即I期和II期,将是预防和治疗胃癌的关键策略。天然产物因其来源丰富、安全性高、药效学机制多样而成为药物开发的重要来源。本文首次对NPs在胃癌发生过程中Correa级联反应的多步骤作用及其调控机制进行了研究和总结。在I期,NPs调节幽门螺杆菌脲酶活性、运动、粘附、毒力因子和耐药性,从而抑制幽门螺杆菌诱导的胃粘膜炎症和氧化应激,促进溃疡愈合。在II期研究中,NPs通过调节胃粘膜细胞周期、细胞凋亡、自噬和血管生成的多种途径和介质,逆转胃癌前病变。在III期,NPs抑制细胞增殖、迁移、侵袭、血管生成和肿瘤干细胞,诱导细胞凋亡和自噬,增强化疗药物敏感性,用于治疗胃癌。与现有工作相比,我们希望发现在胃癌发展的多个阶段具有序治疗作用的NPs,为胃癌的预防、治疗和药物开发提供新的思路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Natural products based on Correa's cascade for the treatment of gastric cancer trilogy: Current status and future perspective.

Gastric carcinoma (GC) is a malignancy with multifactorial involvement, multicellular regulation, and multistage evolution. The classic Correa's cascade of intestinal GC specifies a trilogy of malignant transformation of the gastric mucosa, in which normal gastric mucosa gradually progresses from inactive or chronic active gastritis (Phase I) to gastric precancerous lesions (Phase II) and finally to GC (Phase III). Correa's cascade highlights the evolutionary pattern of GC and the importance of early intervention to prevent malignant transformation of the gastric mucosa. Intervening in early gastric mucosal lesions, i.e., Phase I and II, will be the key strategy to prevent and treat GC. Natural products (NPs) have been an important source for drug development due to abundant sources, tremendous safety, and multiple pharmacodynamic mechanisms. This review is the first to investigate and summarize the multi-step effects and regulatory mechanisms of NPs on the Correa's cascade in gastric carcinogenesis. In phase I, NPs modulate Helicobacter pylori urease activity, motility, adhesion, virulence factors, and drug resistance, thereby inhibiting H. pylori-induced gastric mucosal inflammation and oxidative stress, and facilitating ulcer healing. In Phase II, NPs modulate multiple pathways and mediators regulating gastric mucosal cell cycle, apoptosis, autophagy, and angiogenesis to reverse gastric precancerous lesions. In Phase III, NPs suppress cell proliferation, migration, invasion, angiogenesis, and cancer stem cells, induce apoptosis and autophagy, and enhance chemotherapeutic drug sensitivity for the treatment of GC. In contrast to existing work, we hope to uncover NPs with sequential therapeutic effects on multiple phases of GC development, providing new ideas for gastric cancer prevention, treatment, and drug development.

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