MicroRNA Modulation of Host Immune Response and Inflammation Triggered by
Overview
Chemistry
Molecular Biology
Affiliations
remains the most-researched etiological factor for gastric inflammation and malignancies. Its evolution towards gastric complications is dependent upon host immune response. Toll-like receptors (TLRs) recognize surface and molecular patterns of the bacterium, especially the lipopolysaccharide (LPS), and act upon pathways, which will finally lead to activation of the nuclear factor-kappa B (NF-kB), a transcription factor that stimulates release of inflammatory cytokines. MicroRNAs (MiRNAs) finely modulate TLR signaling, but their expression is also modulated by activation of NF-kB-dependent pathways. This review aims to focus upon several of the most researched miRNAs on this subject, with known implications in host immune responses caused by , including let-7 family, miRNA-155, miRNA-146, miRNA-125, miRNA-21, and miRNA-221. TLR-LPS interactions and their afferent pathways are regulated by these miRNAs, which can be considered as a bridge, which connects gastric inflammation to pre-neoplastic and malignant lesions. Therefore, they could serve as potential non-invasive biomarkers, capable of discriminating infection, as well as its associated complications. Given that data on this matter is limited in children, as well as for as significant number of miRNAs, future research has yet to clarify the exact involvement of these entities in the progression of -associated gastric conditions.
Wang L, Bao J, Yang D, Gao S, He X, He D Curr Microbiol. 2025; 82(4):133.
PMID: 39932559 DOI: 10.1007/s00284-025-04114-3.
Pantic I, Lugonja S, Jerotic D, Pljesa-Ercegovac M, Matic M, Bakovic N Int J Mol Sci. 2025; 26(2.
PMID: 39859205 PMC: 11764725. DOI: 10.3390/ijms26020488.
Srinivasan R, Ramadoss R, Kandasamy V, Ranganadin P, Green S, Kasirajan A Mol Biol Rep. 2025; 52(1):115.
PMID: 39799541 DOI: 10.1007/s11033-024-10214-3.
Wang X, Wang J, Mao L, Yao Y Front Immunol. 2024; 15:1512935.
PMID: 39726601 PMC: 11670821. DOI: 10.3389/fimmu.2024.1512935.
Kuang W, Xu J, Xu F, Huang W, Majid M, Shi H Front Cell Dev Biol. 2024; 12:1513426.
PMID: 39720008 PMC: 11666564. DOI: 10.3389/fcell.2024.1513426.