Cervix carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
In this report, we aimed to explore the roles of gene polymorphisms affecting x-ray repair cross complementing 1 (XRCC1), the tumor protein p53 (TP53), and fibroblast growth factor receptor 3 (FGFR3) in the context of susceptibility to cervical cancer.
|
30616520 |
2019 |
Cervix carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
However, whether the polymorphisms of the BER pathway components (i.e., <i>HOGG1, XRCC1, ADPRT</i>, and <i>APE1</i>) can affect the risk of cervical cancer remains unknown.
|
29156789 |
2017 |
Cervix carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
TGFB1 T10C and XRCC1 G399A SNPs were associated with CC risk in univariate and multivariate analysis and displayed allele-dosage effects and coselection in cancer patients.
|
28906311 |
2017 |
Cervix carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
This meta-analysis showed that the XRCC1 Arg399Gln GA variant might be risk alleles for cervical cancer susceptibility in the Chinese population, and further studies in other ethnic groups are required to arrive at definite conclusions.
|
27487002 |
2017 |
Cervix carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
To conclude, the current meta-analysis indicated that the XRCC1 Arg399Gln polymorphism decreased the risk of cervical cancer, while the Arg194Trp and Arg280His polymorphisms were not associated with cervical caner risk.
|
27903984 |
2017 |
Cervix carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
A positive association was observed between the polymorphisms of XRCC1 genes, that is, in codons 194 [P=0.001, odds ratio (OR)=20.1, 95% confidence interval (CI)=5.9-68.8], 280 (P=0.001, OR=5.4, 95% CI=2.3-12.6), and 399 (P=0.008, OR=4.2, 95% CI=1.5-12.1) and cervical cancer.
|
25812040 |
2016 |
Cervix carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
The Arg399Gln polymorphism in the XRCC1 gene may be related to the increased risk of cervical carcinoma.
|
26345915 |
2015 |
Cervix carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
We searched three electronic databases (MEDLINE, EMBASE and CNKI) for studies on the association between XRCC1 polymorphisms and cervical cancer risk published before June 2013.
|
24057881 |
2014 |
Cervix carcinoma
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
In multivariate logistic regression analysis (adjusting for parity, age at first child birth, use of oral contraceptives, smoking status), low expression of XRCC1, ERCC2, ERCC4, and ERCC1 was associated with a significant increased risk for CC and SIL.
|
23435956 |
2013 |
Cervix carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Gene polymorphism of XRCC1 Arg399Gln and cervical carcinoma susceptibility in Asians: a meta-analysis based on 1,759 cases and 2,497 controls.
|
23534722 |
2013 |
Cervix carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Although the statistical power of our study did not reach 80%, we found a statistically significant association between the XRCC1 399Gln variant and the incidence of cervical cancer.
|
21928248 |
2012 |
Cervix carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Two investigators independently searched the Medline, Embase, CNKI, and Chinese Biomedicine Databases for studies published before March 2011.Summary odds ratios (ORs) and 95% confidence intervals (CIs) for XRCC1 polymorphisms and CC were calculated in a fixed-effects model or a random-effects model when appropriate.
|
22984511 |
2012 |
Cervix carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
The Arg194Trp polymorphism of XRCC1 increases risk of cervical cancer; the variant 399Gln allele predicts poor response to platinum-based chemotherapy, while the Arg194Trp polymorphism indicates a good response.
|
23464469 |
2012 |
Cervix carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
The XRCC1 194Trp/Trp genotype significantly increased the risk for cervical cancer (OR=5.52; 95%CI=1.14-26.64; p=0.03).
|
21790234 |
2011 |
Cervix carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
SNP of XRCC1 gene at codon 399 influences the response of cervical carcinoma to platinum-based NAC.
|
19563645 |
2009 |
Cervix carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
The genotypes of XRCC1 Arginine194Tryptophan and GGH-401Cytosine/Thymine were associated with the response to NAC in patients with cervical cancer.
|
18851872 |
2008 |
Cervix carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
The nonsynonymous single nucleotide polymorphisms of DNA repair gene XRCC1 and susceptibility to the development of cervical carcinoma and high-risk human papillomavirus infection.
|
17504380 |
2007 |
Cervix carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
XRCC1 R399Q polymorphism is associated with response to platinum-based neoadjuvant chemotherapy in bulky cervical cancer.
|
16875718 |
2006 |
Cervix carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Association of XRCC1 Arg399Gln and OGG1 Ser326Cys polymorphisms with the risk of cervical cancer in Japanese subjects.
|
15990162 |
2005 |