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信号转导子和转录激活子 3 基因多态性与中国女性宫颈癌的关联。

Association of signal transducer and activator of transcription 3 gene polymorphisms with cervical cancer in Chinese women.

机构信息

Department of Gynecology and Obstetrics, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.

出版信息

DNA Cell Biol. 2011 Nov;30(11):931-6. doi: 10.1089/dna.2010.1179. Epub 2011 Jun 13.

DOI:10.1089/dna.2010.1179
PMID:21668356
Abstract

Signal transducer and activator of transcription (STAT) plays an important role in regulating cell proliferation, differentiation, and apoptosis. Previous studies revealed that abnormal expression/activation of STAT family members were present in a large group of human malignant tumors. In the present study, using polymerase chain reaction (PCR)-restriction fragment length polymorphism, DNA sequencing, and Taqman probe real-time PCR techniques, we analyzed two single-nucleotide polymorphisms (SNPs) in the STAT5B and STAT3 genes (rs6503691 and rs4769793, respectively) in 275 Chinese cervical cancer patients and 340 controls. Our results indicated that the genotype and allele frequencies of SNP rs4769793 were significantly different between the cervical cancer patients and normal subjects (p < 0.05, odds ratio = 1.35, 95% confidence interval = 1. 07-1.70). In addition, stratified analyses revealed that the polymorphism of rs4769793 was also associated with poor tumor differentiation and positive parametrial invasion (p < 0. 05). In contrast, SNP rs6503691 did not show any difference between patients and controls or association with patient clinical characteristics. Collectively, these findings suggested that STAT3 gene polymorphism (rs4769793) was associated with the susceptibility as well as poor differentiation and parametrial invasion of cervical cancer in Chinese women.

摘要

信号转导子和转录激活子(STAT)在调节细胞增殖、分化和凋亡方面发挥着重要作用。先前的研究表明,STAT 家族成员的异常表达/激活存在于一大群人类恶性肿瘤中。在本研究中,我们使用聚合酶链反应(PCR)-限制性片段长度多态性、DNA 测序和 Taqman 探针实时 PCR 技术,分析了 STAT5B 和 STAT3 基因中的两个单核苷酸多态性(SNPs)(分别为 rs6503691 和 rs4769793)在 275 例中国宫颈癌患者和 340 例对照中的情况。我们的结果表明,SNP rs4769793 的基因型和等位基因频率在宫颈癌患者和正常受试者之间存在显著差异(p<0.05,优势比=1.35,95%置信区间=1.07-1.70)。此外,分层分析显示,rs4769793 多态性也与肿瘤分化不良和阳性宫旁浸润有关(p<0.05)。相比之下,SNP rs6503691 在患者和对照组之间没有差异,也与患者的临床特征无关。总之,这些发现表明 STAT3 基因多态性(rs4769793)与中国女性宫颈癌的易感性以及分化不良和宫旁浸润有关。

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