Roszak Andrzej, Misztal Matthew, Sowińska Anna, Jagodziński Paweł P
Department of Radiotherapy and Gynecological Oncology, Greater Poland Cancer Center, Poznań 61‑866, Poland.
Department of Biochemistry and Molecular Biology, Poznań University of Medical Sciences, Poznań 60‑781, Poland.
Mol Med Rep. 2015 Jun;11(6):4633-8. doi: 10.3892/mmr.2015.3315. Epub 2015 Feb 6.
Although certain studies have demonstrated no association between the stromal cell‑derived factor‑1 (SDF1‑3') G801A single nucleotide polymorphism (SNP) and cervical carcinoma, the interactions between the SDF1‑3' G801A SNP and contraceptive use, menopausal status, parity and tobacco smoking remain to be fully elucidated. Using polymerase chain reaction‑restriction fragment length polymorphism, the distribution of SDF1‑3' G801A genotypes in patients with cervical cancer (n=462) against control groups (n=497) was investigated. Logistic regression analysis, adjusting for age, pregnancy, oral contraceptive use, tobacco smoking and menopausal status, did not identify the SDF1‑3' G801A polymorphism as a genetic risk factor for cervical cancer. The adjusted odds ratio (OR) for patients with the A/G, vs. G/G genotype was 1.203, with a 95% confidence interval (CI) of 0.909‑1.591 (P=0.196). The adjusted OR for the A/A, vs. G/G genotype was 1.296 (95% CI=0.930‑1.807; P=0.125) and for the A/A or A/G, vs. G/G genotype was 1.262 (95% CI=0.964‑1.653; P=0.090)]. The P‑value of the χ2 test of the trend observed for the SDF1‑3' G801A polymorphism was at the borderline of being statistically significant (ptrend=0.0484). Stratified analyses between the distribution of the SDF1‑3' G801A genotypes and cervical cancer risks demonstrated that this polymorphism may be a risk factor for patients with a positive history of tobacco smoking (1.778; 95% CI=1.078‑2.934; P=0.0235). These findings suggested that the SDF1‑3' G801A polymorphism may be a genetic risk factor for cervical cancer in patients with a positive history of tobacco smoking.
尽管某些研究表明基质细胞衍生因子-1(SDF1-3')G801A单核苷酸多态性(SNP)与宫颈癌之间无关联,但SDF1-3' G801A SNP与避孕措施使用、绝经状态、产次及吸烟之间的相互作用仍有待充分阐明。采用聚合酶链反应-限制性片段长度多态性方法,研究了宫颈癌患者(n = 462)与对照组(n = 497)中SDF1-3' G801A基因型的分布情况。在对年龄、妊娠、口服避孕药使用、吸烟及绝经状态进行校正的逻辑回归分析中,未将SDF1-3' G801A多态性确定为宫颈癌的遗传危险因素。A/G基因型患者与G/G基因型患者相比,校正后的比值比(OR)为1.203,95%置信区间(CI)为0.909 - 1.591(P = 0.196)。A/A基因型患者与G/G基因型患者相比,校正后的OR为1.296(95% CI = 0.93