Unknown

Dataset Information

0

Characterization and strong risk association of TLR2 del -196 to -174 polymorphism and Helicobacter pylori and their influence on mRNA expression in gastric cancer.


ABSTRACT: BACKGROUND:Toll-like receptor-2 (TLR2) is responsible for recognizing Helicobacter pylori (H. pylori) and activating the immune response. Polymorphisms in TLR2 may modulate gastric carcinogenesis. AIM:To evaluate whether the TLR2 19216T/C (rs3804099) and TLR2 -196 to -174 ins/del (rs111200466) polymorphisms contribute to gastric carcinogenesis in the Brazilian population, and to determine the influence of both polymorphisms and H. pylori infection on TLR2 mRNA expression. METHODS:DNA was extracted from 854 peripheral blood leukocyte or gastric tissue samples [202 gastric cancer (GC), 269 chronic gastritis (CG), and 383 control/healthy (C)] and genotyped by allele-specific PCR or restriction fragment length polymorphism (RFLP)-PCR. Quantitative polymerase chain reaction by TaqMan® assay was used to quantify TLR2 mRNA levels in fresh gastric tissues (48 GC, 36 CG, and 14 C). RESULTS:Regarding the TLR2 -196 to -174 polymorphism, the ins/del and del/del genotypes were associated with a higher risk of GC by comparison with the C in all of the analyzed inheritance models (codominant, dominant, recessive, overdominant and log-additive; P < 0.0001). Similarly, an increased risk was observed when comparing the GC and CG groups [codominant (P < 0.0001), dominant (P < 0.0001), recessive (P = 0.0260), overdominant (P < 0.0001) and log-additive (P < 0.0001)]. In contrast, TLR2 19216T/C was associated with a protective effect in the GC group compared to the C group [dominant (P = 0.0420) and log-additive (P = 0.0300)]. Regarding the association of polymorphisms with H. pylori infection, individuals infected with H. pylori and harboring the TLR2 -196 to -174 ins/del polymorphism had an increased risk of gastric carcinogenesis [codominant (P = 0.0120), dominant (P = 0.0051), overdominant (P = 0.0240) and log-additive (P = 0.0030)], while TLR2 19216T/C was associated with a protective effect [codominant (P = 0.0039), dominant (P < 0.0001), overdominant (P = 0.0097) and log-additive (P = 0.0021)]. TLR2 mRNA levels were significantly increased in the GC group (median RQ = 6.95) compared to the CG group (RQ = 0.84, P < 0.0001) and to the normal mucosa group (RQ = 1.0). In addition, both H. pylori infection (P < 0.0001) and the presence of the polymorphic TLR2 -196 to -174del (P = 0.0010) and TLR2 19216 C (P = 0.0004) alleles influenced TLR2 mRNA expression. CONCLUSION:The TLR2 -196 to -174 ins/del and TLR2 19216 T/C polymorphisms are strongly associated with GC. TLR2 mRNA expression levels are upregulated in neoplastic tissues and influenced by both the presence of H. pylori and variant genotypes.

SUBMITTER: Lourenco CM 

PROVIDER: S-EPMC7235183 | biostudies-literature | 2020 May

REPOSITORIES: biostudies-literature

altmetric image

Publications

Characterization and strong risk association of <i>TLR2 del -196</i> to <i>-174</i> polymorphism and <i>Helicobacter pylori</i> and their influence on mRNA expression in gastric cancer.

Lourenço Caroline de Matos CM   Susi Manoela Dias MD   do Nascimento Mariah Cristina Antunes MCA   Serafim Junior Vilson V   Vila Ana Paula Simedan APS   Rodrigues-Flemming Gabriela Helena GH   Goloni-Bertollo Eny Maria EM   Silva Ana Elizabete AE   de Oliveira-Cucolo Juliana Garcia JG  

World journal of gastrointestinal oncology 20200501 5


<h4>Background</h4>Toll-like receptor-2 (<i>TLR2</i>) is responsible for recognizing <i>Helicobacter pylori</i> (<i>H. pylori</i>) and activating the immune response. Polymorphisms in <i>TLR2</i> may modulate gastric carcinogenesis.<h4>Aim</h4>To evaluate whether the <i>TLR2 19216T/C</i> (rs3804099) and <i>TLR2</i> -<i>196 to -174 ins/del</i> (rs111200466) polymorphisms contribute to gastric carcinogenesis in the Brazilian population, and to determine the influence of both polymorphisms and <i>H  ...[more]

Similar Datasets

| S-EPMC6745549 | biostudies-literature
| S-EPMC3203069 | biostudies-literature
| S-EPMC4735314 | biostudies-literature
| S-EPMC4678392 | biostudies-literature
| S-EPMC8938428 | biostudies-literature
| S-EPMC3772856 | biostudies-literature
| S-EPMC3128813 | biostudies-literature
2018-11-23 | PXD009583 | Pride
| S-EPMC10921109 | biostudies-literature
| S-EPMC8177986 | biostudies-literature