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幽门螺杆菌相关胃癌发生的研究进展

Advances in Gastric Carcinogenesis Related to Helicobacter Pylori.

作者信息

Chivu Roxana-Florentina, Melesteu Carmen, Bobirca Anca, Dumitrescu Dan-Andrei, Melesteu Ionut, Mustatea Petronel, Bobirca Florin, Patrascu Traian

出版信息

Chirurgia (Bucur). 2025 Jun;120(3):322-344. doi: 10.21614/chirurgia.3147.

Abstract

Helicobacter pylori (H. pylori), a Gram-negative bacterium, has been classified as a Group I carcinogen by the World Health Organization. It represents the most significant modifiable risk factor for gastric cancer (GC), particularly the intestinal subtype. Although global infection rates are on the decline, its role in gastric oncogenesis remains prominent, especially in areas with elevated incidence rates. This review consolidates current insights into the molecular and immunological pathways through which H. pylori contributes to gastric tumorigenesis, with a focus on epigenetic modulation, host-microbe interactions, and the influence of the gastric microbiota. Chronic inflammation, instigated by H. pylori infection, advances through the Correa cascade, culminating in neoplastic transformation. Principal virulence determinants, including CagA and VacA, compromise epithelial barriers and initiate oncogenic signaling networks such as NF-úB, STAT3, Wnt/ò-catenin, and Hippo/YAP. The infection is also associated with extensive epigenetic remodeling, notably promoter hypermethylation of tumor suppressor genes like CDH1, and regulation of non-coding RNAs (including miRNAs, lncRNAs, and circRNAs). Sustained colonization drives immune polarization toward Th1 and Th17 responses, promotes immune escape mechanisms such as PD-L1 overexpression, and alters the composition of the gastric microbiome. Recent findings highlight the potential role of non-H. pylori microbial species in supporting tumor progression. While eradication of H. pylori lowers the risk of gastric cancer, it does not confer complete protection, particularly in individuals with pre-existing mucosal alterations or microbial dysbiosis. The development of H. pylori-associated gastric cancer is a multifactorial process, shaped by microbial virulence, host genetics, epigenetic shifts, and immune dynamics. A deeper understanding of these interrelated mechanisms is crucial for refining preventive measures, diagnostic accuracy, and therapeutic approaches.

摘要

幽门螺杆菌(H. pylori)是一种革兰氏阴性菌,已被世界卫生组织列为I类致癌物。它是胃癌(GC),尤其是肠型胃癌最重要的可改变风险因素。尽管全球感染率呈下降趋势,但其在胃癌发生中的作用仍然突出,特别是在发病率较高的地区。本综述整合了目前对幽门螺杆菌促进胃癌发生的分子和免疫途径的见解,重点关注表观遗传调控、宿主-微生物相互作用以及胃微生物群的影响。幽门螺杆菌感染引发的慢性炎症通过科雷亚级联反应发展,最终导致肿瘤转化。主要毒力决定因素,包括细胞毒素相关基因A(CagA)和空泡毒素A(VacA),破坏上皮屏障并启动致癌信号网络,如核因子κB(NF-κB)、信号转导子和转录激活子3(STAT3)、Wnt/β-连环蛋白以及Hippo/Yes相关蛋白(YAP)。这种感染还与广泛的表观遗传重塑有关,特别是肿瘤抑制基因如E-钙黏蛋白(CDH1)的启动子高甲基化,以及非编码RNA(包括微小RNA、长链非编码RNA和环状RNA)的调控。持续定植促使免疫反应向辅助性T细胞1(Th1)和辅助性T细胞17(Th17)极化,促进免疫逃逸机制,如程序性死亡受体配体1(PD-L1)过表达,并改变胃微生物群的组成。最近的研究结果突出了非幽门螺杆菌微生物物种在支持肿瘤进展中的潜在作用。虽然根除幽门螺杆菌可降低胃癌风险,但并不能提供完全保护,特别是在已有黏膜改变或微生物失调的个体中。幽门螺杆菌相关胃癌的发生是一个多因素过程,受微生物毒力、宿主遗传学、表观遗传变化和免疫动态影响。深入了解这些相互关联的机制对于完善预防措施、诊断准确性和治疗方法至关重要。

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