Primary malignant neoplasm of lung
|
|
0.030 |
GeneticVariation
|
BEFREE |
In the gene encoding RAGE (<i>AGER</i>), there are three well-known polymorphisms; rs2070600, rs1800624, and rs1800625, which potentially increase the risk of lung cancer.
|
29212235 |
2017 |
Carcinoma of lung
|
|
0.030 |
GeneticVariation
|
BEFREE |
In the gene encoding RAGE (<i>AGER</i>), there are three well-known polymorphisms; rs2070600, rs1800624, and rs1800625, which potentially increase the risk of lung cancer.
|
29212235 |
2017 |
Malignant neoplasm of lung
|
|
0.030 |
GeneticVariation
|
BEFREE |
In the gene encoding RAGE (<i>AGER</i>), there are three well-known polymorphisms; rs2070600, rs1800624, and rs1800625, which potentially increase the risk of lung cancer.
|
29212235 |
2017 |
Malignant neoplasm of lung
|
|
0.030 |
GeneticVariation
|
BEFREE |
But in subgroup analysis, the rs1800624 polymorphism significantly increased lung cancer susceptibility in the homozygous model (OR=1.486, 95%CI:1.147-1.924, p=0.003) and the allele model (OR=1.15, 95%CI:1.029-1.285, p=0.014), but most likely contributed to decreased susceptibility to breast cancer in the allele model (OR=0.791 95%CI: 0.648-0.965, p=0.021), the heterozygous model (OR=0.733, 95%CI:0.577-0.931, p=0.011) and the dominant model (OR=0.741, 95%CI:0.588-0.934, p=0.011).
|
26011358 |
2015 |
Primary malignant neoplasm of lung
|
|
0.030 |
GeneticVariation
|
BEFREE |
But in subgroup analysis, the rs1800624 polymorphism significantly increased lung cancer susceptibility in the homozygous model (OR=1.486, 95%CI:1.147-1.924, p=0.003) and the allele model (OR=1.15, 95%CI:1.029-1.285, p=0.014), but most likely contributed to decreased susceptibility to breast cancer in the allele model (OR=0.791 95%CI: 0.648-0.965, p=0.021), the heterozygous model (OR=0.733, 95%CI:0.577-0.931, p=0.011) and the dominant model (OR=0.741, 95%CI:0.588-0.934, p=0.011).
|
26011358 |
2015 |
Carcinoma of lung
|
|
0.030 |
GeneticVariation
|
BEFREE |
But in subgroup analysis, the rs1800624 polymorphism significantly increased lung cancer susceptibility in the homozygous model (OR=1.486, 95%CI:1.147-1.924, p=0.003) and the allele model (OR=1.15, 95%CI:1.029-1.285, p=0.014), but most likely contributed to decreased susceptibility to breast cancer in the allele model (OR=0.791 95%CI: 0.648-0.965, p=0.021), the heterozygous model (OR=0.733, 95%CI:0.577-0.931, p=0.011) and the dominant model (OR=0.741, 95%CI:0.588-0.934, p=0.011).
|
26011358 |
2015 |
Malignant neoplasm of lung
|
|
0.030 |
GeneticVariation
|
BEFREE |
Haplotype C-A-A (alleles in order of rs1800625, rs1800624 and rs2070600) of RAGE gene was overrepresented in patients, and conferred a 2.1-fold increased risk of lung cancer (95% confidence interval: 1.52-2.91), independent of confounding factors.
|
23874853 |
2013 |
Carcinoma of lung
|
|
0.030 |
GeneticVariation
|
BEFREE |
Haplotype C-A-A (alleles in order of rs1800625, rs1800624 and rs2070600) of RAGE gene was overrepresented in patients, and conferred a 2.1-fold increased risk of lung cancer (95% confidence interval: 1.52-2.91), independent of confounding factors.
|
23874853 |
2013 |
Primary malignant neoplasm of lung
|
|
0.030 |
GeneticVariation
|
BEFREE |
Haplotype C-A-A (alleles in order of rs1800625, rs1800624 and rs2070600) of RAGE gene was overrepresented in patients, and conferred a 2.1-fold increased risk of lung cancer (95% confidence interval: 1.52-2.91), independent of confounding factors.
|
23874853 |
2013 |
Breast Carcinoma
|
|
0.020 |
GeneticVariation
|
BEFREE |
Our findings altogether demonstrate a significant association between RAGE gene rs1800624 polymorphism and breast cancer risk, and more importantly a cumulative impact of multiple risk associated polymorphisms in HMGB1/RAGE pathway on breast carcinogenesis.
|
27241711 |
2016 |
Malignant neoplasm of breast
|
|
0.020 |
GeneticVariation
|
BEFREE |
Our findings altogether demonstrate a significant association between RAGE gene rs1800624 polymorphism and breast cancer risk, and more importantly a cumulative impact of multiple risk associated polymorphisms in HMGB1/RAGE pathway on breast carcinogenesis.
|
27241711 |
2016 |
Malignant neoplasm of breast
|
|
0.020 |
GeneticVariation
|
BEFREE |
But in subgroup analysis, the rs1800624 polymorphism significantly increased lung cancer susceptibility in the homozygous model (OR=1.486, 95%CI:1.147-1.924, p=0.003) and the allele model (OR=1.15, 95%CI:1.029-1.285, p=0.014), but most likely contributed to decreased susceptibility to breast cancer in the allele model (OR=0.791 95%CI: 0.648-0.965, p=0.021), the heterozygous model (OR=0.733, 95%CI:0.577-0.931, p=0.011) and the dominant model (OR=0.741, 95%CI:0.588-0.934, p=0.011).
|
26011358 |
2015 |
Breast Carcinoma
|
|
0.020 |
GeneticVariation
|
BEFREE |
But in subgroup analysis, the rs1800624 polymorphism significantly increased lung cancer susceptibility in the homozygous model (OR=1.486, 95%CI:1.147-1.924, p=0.003) and the allele model (OR=1.15, 95%CI:1.029-1.285, p=0.014), but most likely contributed to decreased susceptibility to breast cancer in the allele model (OR=0.791 95%CI: 0.648-0.965, p=0.021), the heterozygous model (OR=0.733, 95%CI:0.577-0.931, p=0.011) and the dominant model (OR=0.741, 95%CI:0.588-0.934, p=0.011).
|
26011358 |
2015 |
Diabetes Mellitus, Non-Insulin-Dependent
|
|
0.020 |
GeneticVariation
|
BEFREE |
However, the AA genotype of SNP rs1800624 (-374T/A) was consistently associated with lower SBP [-5.0 mmHg (95% confidence interval -10.4 to 0.3)] and DBP [-4.2 (-7.2 to -1.3)], pulse pressure [-0.8 (-5.0 to 3.4)] as well as with less arterial stiffness [-0.56 SD (-1.04 to -0.09)] in individuals with normal glucose metabolism, but with higher SBP [6.2 (0.9-11.5)], DBP [2.1 (-0.7 to 5.0)] and pulse pressure [4.1 (-0.2 to 8.4)] in individuals with impaired glucose metabolism or type 2 diabetes mellitus (P for interaction <or=0.05 in all analyses).
|
20051912 |
2010 |
Diabetes Mellitus, Non-Insulin-Dependent
|
|
0.020 |
GeneticVariation
|
BEFREE |
We investigated the relationship of 3 polymorphisms (rs1800625, rs1800624 and rs2070600) in the AGER gene and their haplotypes with T2DM as well as insulin resistance.
|
18796298 |
2008 |
Asthma
|
|
0.010 |
GeneticVariation
|
BEFREE |
Haplotype analysis revealed that haplotype T-A-G-T (allele order: rs1800625, rs1800624, rs2070600, rs184003) was significantly associated with a reduced COPD risk (OR=0.32, 95% CI: 0.06-0.60), and haplotype T-A-A-G was significantly associated with a reduced asthma risk (OR=0.19, 95% CI: 0.04-0.96).
|
31141790 |
2019 |
Heart Diseases
|
|
0.010 |
GeneticVariation
|
BEFREE |
The rs1800624 SNP involves <i>AGER</i> gene regulation and may be related to reduced risk of heart disease, cancer, Crohn's disease, and type 1 diabetes complications.
|
30863465 |
2019 |
Chronic Obstructive Airway Disease
|
|
0.010 |
GeneticVariation
|
BEFREE |
In single-locus analysis, there was significant difference in the genotype distributions of rs1800624 between COPD patients and controls (<i>p</i>=0.022), and the genotype and allele distributions of rs1800625 differed significantly (<i>p</i>=0.040 and 0.016) between asthma patients and controls.
|
31141790 |
2019 |
Complications of Diabetes Mellitus
|
|
0.010 |
GeneticVariation
|
BEFREE |
The rs1800624 SNP involves <i>AGER</i> gene regulation and may be related to reduced risk of heart disease, cancer, Crohn's disease, and type 1 diabetes complications.
|
30863465 |
2019 |
Diabetes Mellitus, Insulin-Dependent
|
|
0.010 |
GeneticVariation
|
BEFREE |
The rs1800624 SNP involves <i>AGER</i> gene regulation and may be related to reduced risk of heart disease, cancer, Crohn's disease, and type 1 diabetes complications.
|
30863465 |
2019 |
Cervix carcinoma
|
|
0.010 |
GeneticVariation
|
BEFREE |
In conclusion, RAGE SNPs rs1800624 was associated with some clinicopathological variables in cervical cancer.
|
30410591 |
2018 |
Age related macular degeneration
|
|
0.010 |
GeneticVariation
|
BEFREE |
CONCLUSIONS We revealed a significant association between RAGE gene rs1800624 and rs1800625 polymorphisms and AMD risk.
|
29317590 |
2018 |
Tumor Cell Invasion
|
|
0.010 |
GeneticVariation
|
BEFREE |
Moreover, cervical cancer patients with genotypes TA/AA in rs1800624 exhibited a lower risk of parametrium invasion, moderate-to-poor cell differentiation, and pelvic lymph node metastasis.
|
30410591 |
2018 |
Secondary malignant neoplasm of lymph node
|
|
0.010 |
GeneticVariation
|
BEFREE |
Moreover, cervical cancer patients with genotypes TA/AA in rs1800624 exhibited a lower risk of parametrium invasion, moderate-to-poor cell differentiation, and pelvic lymph node metastasis.
|
30410591 |
2018 |
cervical cancer
|
|
0.010 |
GeneticVariation
|
BEFREE |
In conclusion, RAGE SNPs rs1800624 was associated with some clinicopathological variables in cervical cancer.
|
30410591 |
2018 |