TY - JOUR
T1 - G801A Polymorphism of human stromal cell-derived factor 1 gene raises no susceptibility to neoplastic lesions of uterine cervix
AU - Tee, Yi Torng
AU - Yang, Shun Fa
AU - Wang, Po Hui
AU - Tsai, Hsiu Ting
AU - Lin, Long Yau
AU - Lee, Shu Kuei
AU - Liao, Chiung Ling
AU - Chang, Jinghau Tsai
AU - Shih, Yang Tse
PY - 2012
Y1 - 2012
N2 - Objective: This study aimed to investigate the association of stromal cellYderived factor 1 (SDF-1) gene polymorphisms with the neoplastic lesions of uterine cervix in Mid-Taiwan women. Materials and Methods: Four hundred ninety-eight blood samples were collected from 161 patients with neoplasia of uterine cervix, including 76 cancer patients, 61 patients with high-grade dysplasia, and 24 with low-grade dysplasia, and 337 healthy controls who lived in Mid-Taiwan. Polymorphism of the SDF-1 gene was examined using polymerase chain reactionYrestriction fragment length polymorphism. Results: For SDF-1 gene polymorphisms, the wild-type homozygous alleles (G/G) yielded 100- and 193-bp products, the heterozygous alleles (G/A) yielded 100-, 193- and 293-bp products, whereas the mutated-type homozygous alleles (A/A) yielded a 293-bp product. We found no significant difference in genotypes or alleles distribution of SDF-1 polymorphisms between patients with cervical neoplasia and healthy women (P = 0.530). Compared with the homozygous GG subgroup, GA and AA subgroups do not increase the risk of cervical neoplasia. Conclusions: Although the expression of SDF-1 was reported to be significantly increased in cervical carcinogenesis in previous studies, our results, however, show that SDF-1 gene polymorphism could not be considered as a factor related to an increased susceptibility to cervical neoplasia.
AB - Objective: This study aimed to investigate the association of stromal cellYderived factor 1 (SDF-1) gene polymorphisms with the neoplastic lesions of uterine cervix in Mid-Taiwan women. Materials and Methods: Four hundred ninety-eight blood samples were collected from 161 patients with neoplasia of uterine cervix, including 76 cancer patients, 61 patients with high-grade dysplasia, and 24 with low-grade dysplasia, and 337 healthy controls who lived in Mid-Taiwan. Polymorphism of the SDF-1 gene was examined using polymerase chain reactionYrestriction fragment length polymorphism. Results: For SDF-1 gene polymorphisms, the wild-type homozygous alleles (G/G) yielded 100- and 193-bp products, the heterozygous alleles (G/A) yielded 100-, 193- and 293-bp products, whereas the mutated-type homozygous alleles (A/A) yielded a 293-bp product. We found no significant difference in genotypes or alleles distribution of SDF-1 polymorphisms between patients with cervical neoplasia and healthy women (P = 0.530). Compared with the homozygous GG subgroup, GA and AA subgroups do not increase the risk of cervical neoplasia. Conclusions: Although the expression of SDF-1 was reported to be significantly increased in cervical carcinogenesis in previous studies, our results, however, show that SDF-1 gene polymorphism could not be considered as a factor related to an increased susceptibility to cervical neoplasia.
KW - Neoplasia of uterine cervix
KW - Single nucleotide polymorphisms
KW - Stromal cell-derived factor 1 gene
UR - http://www.scopus.com/inward/record.url?scp=84867243811&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84867243811&partnerID=8YFLogxK
U2 - 10.1097/IGC.0b013e318265d334
DO - 10.1097/IGC.0b013e318265d334
M3 - Article
C2 - 22954782
AN - SCOPUS:84867243811
SN - 1048-891X
VL - 22
SP - 1297
EP - 1302
JO - International Journal of Gynecological Cancer
JF - International Journal of Gynecological Cancer
IS - 8
ER -