Diversification and deleterious role of microbiome in gastric cancer
- PMID: 37530125
- PMCID: PMC10644335
- DOI: 10.1002/cnr2.1878
Diversification and deleterious role of microbiome in gastric cancer
Abstract
Gut microbiota dictates the fate of several diseases, including cancer. Most gastric cancers (GC) belong to gastric adenocarcinomas (GAC). Helicobacter pylori colonizes the gastric epithelium and is the causative agent of 75% of all stomach malignancies globally. This bacterium has several virulence factors, including cytotoxin-associated gene A (CagA), vacuolating cytotoxin (VacA), and outer membrane proteins (OMPs), all of which have been linked to the development of gastric cancer. In addition, bacteria such as Escherichia coli, Streptococcus, Clostridium, Haemophilus, Veillonella, Staphylococcus, and Lactobacillus play an important role in the development of gastric cancer. Besides, lactic acid bacteria (LAB) such as Bifidobacterium, Lactobacillus, Lactococcus, and Streptococcus were found in greater abundance in GAC patients. To identify potential diagnostic and therapeutic interventions for GC, it is essential to understand the mechanistic role of H. pylori and other bacteria that contribute to gastric carcinogenesis. Furthermore, understanding bacteria-host interactions and bacteria-induced inflammatory pathways in the host is critical for developing treatment targets for gastric cancer.
Keywords: Helicobacter pylori; bacterial metabolites; gastric cancer; gut microbiome.
© 2023 The Authors. Cancer Reports published by Wiley Periodicals LLC.
Conflict of interest statement
The authors have stated explicitly that there are no conflicts of interest in connection with this article.
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