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Polymorphisms at Locus 4p14 of Toll-Like Receptors TLR-1 and TLR-10 Confer Susceptibility to Gastric Carcinoma in Helicobacter pylori Infection
Author(s) -
M. Ravishankar Ram,
KheanLee Goh,
Alex HwongRuey Leow,
Bee Hoon Poh,
Mun Fai Loke,
R. A. Harrison,
Esaki M. Shankar,
Jamuna Vadivelu
Publication year - 2015
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0141865
Subject(s) - helicobacter pylori , single nucleotide polymorphism , immunology , gastritis , inflammation , toll like receptor , disease , biology , genotype , proinflammatory cytokine , medicine , immune system , gene , innate immune system , genetics
Helicobacter pylori ( H . pylori ) - induced gastric inflammation impacts the functions of leptin- and ghrelin-producing cells in the gastroduodenum. Inflammation resulting from H . pylori sensing via Toll-like receptors (TLRs) and the associated downstream signaling largely remain ambiguous. Here, we investigated the role of gut hormones, pro-inflammatory cytokines and single nucleotide polymorphisms (SNPs) associated with TLR 4p14 in H . pylori disease in 30 subjects with non-ulcer dyspepsia (NUD), 40 with peptic ulcer disease (PUD) and 15 with gastric cancer (GC) subjects positive and negative for H . pylori infection. The level of pro-inflammatory cytokines was directly proportional to the severity of gastritis, and disease status influenced the levels of gut hormones and pro-inflammatory cytokines. TLR-1 SNPs rs4833095 and TLR-10 SNPs rs10004195 and were directly associated with H . pylori disease, and were up-regulated in the presence of H . pylori in a genotype-independent manner. We concluded that TLR-1 rs4833095 and TLR10 rs10004195 confer susceptibility to development of gastroduodenal disease, especially GC in H . pylori disease.

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