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Genetic polymorphisms in MMP 2, 3, 7, and 9 genes and the susceptibility and clinical outcome of cervical cancer in a Chinese Han population

机译:中国汉族人群MMP 2、3、7和9基因多态性与宫颈癌的易感性和临床结局

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Matrix metalloproteases (MMPs) are proteolytic enzymes that contribute to all stages of tumor progression, including the invasion and metastasis. However, there are no data about the role of MMP polymorphism in the development of cervical cancer. A hospital-based case-control study was conducted in 230 patients with cervical cancer and 230 healthy controls to investigate the possible association between the MMP2 rs243865, MMP3 rs3025058, MMP7 rs11568818, and MMP9 rs3918242 polymorphisms, respectively, and the risk of cervical cancer. Our results suggested that the MMP2 rs243865-1306 C/T was significantly associated with an increased risk of cervical cancer (CT vs. CC, OR = 1.46; 95 % CI 1.18-3.55; P = 0.032; TT vs. CC, OR = 1.72; 95 % CI 1.28-4.02; P = 0.031; CT + TT vs. CC, OR = 1.43; 95 % CI 1.21-3.44; P = 0.029). Similarly, the MMP7 rs11568818-181A/G genotypes can also elevate the risk of cervical cancer in all genetic models. However, the genotype and allele frequencies of MMP3 rs3025058 and MMP9 rs3918242 polymorphisms in cervical cancer patients were not significantly different from controls. Further analysis showed MMP2 rs243865 and MMP7 rs11568818 genotypes were associated with advanced tumor stages of cervical cancer patients. More interestingly, the MMP2 rs243865 and MMP7 rs11568818 genotype was statistically significantly associated with a poor survival in cervical cancer patients. Our results showed that the MMP2 rs243865 and MMP7 rs11568818 genotypes e were associated with increased susceptibility and development of cervical cancer in Chinese Han population.
机译:基质金属蛋白酶(MMP)是蛋白水解酶,可参与肿瘤进展的所有阶段,包括侵袭和转移。但是,没有关于MMP多态性在宫颈癌发展中的作用的数据。一项基于医院的病例对照研究对230位宫颈癌患者和230位健康对照者进行了研究,以调查MMP2 rs243865,MMP3 rs3025058,MMP7 rs11568818和MMP9 rs3918242多态性与宫颈癌风险之间的可能关联。我们的结果表明,MMP2 rs243865-1306 C / T与宫颈癌风险的增加显着相关(CT vs. CC,OR = 1.46; 95%CI 1.18-3.55; P = 0.032; TT vs. CC,OR = 1.72; 95%CI 1.28-4.02; P = 0.031; CT + TT对CC,OR = 1.43; 95%CI 1.21-3.44; P = 0.029)。同样,在所有遗传模型中,MMP7 rs11568818-181A / G基因型也可提高子宫颈癌的风险。但是,宫颈癌患者中MMP3 rs3025058和MMP9 rs3918242多态性的基因型和等位基因频率与对照组无显着差异。进一步的分析表明,MMP2 rs243865和MMP7 rs11568818基因型与宫颈癌患者的晚期肿瘤分期有关。更有趣的是,MMP2 rs243865和MMP7 rs11568818基因型与宫颈癌患者的不良生存率在统计学上显着相关。我们的结果表明,MMP2 rs243865和MMP7 rs11568818基因型e与中国汉族人群宫颈癌的易感性和发展有关。

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