Stomach Carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
The IL-1RA downregulated the metastatic potential of gastric cancer through blockage of the IL-1α/VEGF signaling pathways.
|
29344744 |
2018 |
Stomach Carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
There was a positive correlation between IL-1α, which was upregulated during hypoxia, and tumor stage, lymph node metastasis and resistance to cisplatin in GC.
|
28608600 |
2017 |
Stomach Carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
The pro-inflammatory cytokine IL-1β plays a crucial role in the development of gastric tumors, and polymorphisms in the IL-1 gene cluster resulting in increased IL-1β production have been associated with increased risk for gastric cancer.
|
27460807 |
2016 |
Stomach Carcinoma
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
The effect of IL1B was assessed by studying the expression and activation status of the IL1Β-activated transcription factors C/EBPβ and CREB in GC cell lines.
|
25740226 |
2016 |
Stomach Carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
These findings suggest that functional polymorphism rs3783553 in IL-1A could contribute to GC susceptibility, possibly or at least partially through affecting the transcriptional activity of IL-1A.
|
26889982 |
2016 |
Stomach Carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
These results suggested that SNPs in the IL-1 family genes play important roles in the development of GC and the IL-1F5 might be the target gene of miR-197, and miR-197 might negatively regulate its expression.
|
26632693 |
2015 |
Stomach Carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Inflammation, especially the cytokine response of the IL-1 family, has been shown to influence susceptibility to gastric cancer.
|
24557417 |
2015 |
Stomach Carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
The haplotype analysis of the IL1A LD block in the combined dataset revealed the association between a common haplotype carrying the rs17042407 variant and GC, particularly of the intestinal type (p = 3.1 × 10(-5) ) and non cardia localisation (p = 4.6 × 10(-3) ).
|
24615437 |
2014 |
Stomach Carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
A functional polymorphism in IL-1A gene is associated with a reduced risk of gastric cancer.
|
23900673 |
2014 |
Stomach Carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
The proinflammatory cytokine IL-1β plays a crucial role in the development of gastric tumors and polymorphisms in the IL-1 gene cluster leading to increased IL-1β production have been associated with increased risk for gastric cancer.
|
25172489 |
2014 |
Stomach Carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Polymorphisms within interleukin-1 (IL1) and tumor necrosis factor alpha (TNFA) gene clusters are associated with an increased risk of gastric cancer.
|
20200422 |
2010 |
Stomach Carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Proinflammatory genotypes of the IL-1 (interleukin-1) gene have been associated with an increased gastric cancer risk in Caucasians, whereas some studies in Asian populations did not find such association.
|
17596959 |
2007 |
Stomach Carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
The purpose of this study was to examine the association between IL-1 genotype and gastric cancer by systematically reviewing the risk of the original studies.
|
17096351 |
2007 |
Stomach Carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
In countries with a low prevalence of gastric cancer, risk groups carrying cagA+ strains and IL-1 genetic polymorphisms should be identified and treated.
|
17006981 |
2006 |
Stomach Carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
We tested for an association between IL-1 loci polymorphisms with increased gastric mucosal levels of IL-1beta and an increased risk of developing GC in a Korean population.
|
15551344 |
2005 |
Stomach Carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Interkeukin-1 (IL-1) gene cluster polymorphisms that are thought to enhance the production of IL-1beta are associated with an increased risk of gastric cancer.
|
16143884 |
2005 |
Stomach Carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
There was no correlation between H. pylori infection and IL-1 gene polymorphism in GC.
|
15688413 |
2005 |
Stomach Carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
The aim of the study was to investigate the relationship between selected IL1 loci polymorphisms and gastric cancer risk in an Italian population.
|
16128937 |
2005 |
Stomach Carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Our aim was to evaluate whether IL-1 gene cluster and tumor necrosis factor-alpha (TNFA)-307 polymorphisms, as well as cagA-positive status, are associated with gastric carcinoma in a non-Caucasian population by analyzing the data in logistic regression models.
|
15704154 |
2005 |
Stomach Carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
In conclusion, IL-1beta, IL1-RN, and TNF-alpha genotypes are not associated with gastric cancer in Italian patients.
|
15927855 |
2005 |
Stomach Carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
In advanced gastric cancer (tumor stages T2-T4), associations with polymorphisms of the interleukin-1 (IL-1) gene cluster have been made.
|
15570075 |
2004 |
Stomach Carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
The aim of this study was to prospectively investigate the relationship between selected polymorphisms in three of the major IL-1 gene family members, seeking associations with H. pylori infection and/or gastric cancer.
|
15481335 |
2004 |
Stomach Carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
To elucidate the risks of host interleukin-1 (IL-1) genetic polymorphisms and H. pylori infection in the development of gastric cancer.
|
15233701 |
2004 |
Stomach Carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
No association was noted between GC and controls in the distribution of IL-1 and TNF-alpha genotypes.
|
12594817 |
2003 |
Stomach Carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
The involvement of proinflammatory cytokines (especially IL-1 and IL-8) and reactive oxygen species (ROS) due to NF kappa B activation, increased cell proliferation combined with inhibition of apoptosis as well as upregulation of peroxisome proliferation activated receptor gamma (PPAR gamma) and inducible nitric oxide synthase (iNOS) appear to be major molecular biology alterations in pathogenesis of GC.
|
12883469 |
2003 |