2015
DOI: 10.3892/mmr.2015.3315
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Stromal cell-derived factor-1 G801A polymorphism and the risk factors for cervical cancer

Abstract: Abstract.Although certain studies have demonstrated no association between the stromal cell-derived factor-1 (SDF1-3')

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Cited by 3 publications
(3 citation statements)
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“…A higher frequency of HPV was observed among allele A carriers, confirmed by binary logistic regression model adjusted for several factors as confounders, demonstrating that CXCL12 rs1801157 is independently associated to HPV infection. Some studies observed that the polymorphism was not a risk factor for cervical cancer development [ 13 , 14 , 27 ] however, none of them have evaluated whether the polymorphism could represent a risk factor for HPV infection as demonstrated in this study.…”
Section: Discussionmentioning
confidence: 78%
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“…A higher frequency of HPV was observed among allele A carriers, confirmed by binary logistic regression model adjusted for several factors as confounders, demonstrating that CXCL12 rs1801157 is independently associated to HPV infection. Some studies observed that the polymorphism was not a risk factor for cervical cancer development [ 13 , 14 , 27 ] however, none of them have evaluated whether the polymorphism could represent a risk factor for HPV infection as demonstrated in this study.…”
Section: Discussionmentioning
confidence: 78%
“…In a case-control study the rs1801157 polymorphism was not associated with invasive squamous carcinoma and adenocarcinoma in situ [ 13 ]. On the other hand, analysis between this polymorphism genotype distribution and cervical cancer risk, showed that allele A of this polymorphism may be a risk factor for patients with a positive history of tobacco smoking [ 14 ].…”
Section: Introductionmentioning
confidence: 99%
“…In addition, a silent sequence variant with a C/T substitution (+414 C > T; rs2228014) has been found in medulloblastomas, with no association between the +414 C>T variant and the subtype of medulloblastomas (30). Until now, numerous studies have reported that SDF-1 rs1801157 and CXCR4 rs2228014 are significantly associated with susceptibility to carcinogenesis in humans (28,(31)(32)(33)(34)(35)(36)(37)(38). However, the association of SDF-1 and CXCR4 polymorphisms with the risk and the clinicopathological development of OPSCC remain inconclusive and controversial (39,40).…”
mentioning
confidence: 99%