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Bladder Cancer Risk Associated with Genotypic Polymorphism of the Matrix Metalloproteinase-1 and 7 in North Indian Population

机译:与北部印度人群基质金属蛋白酶-1和7基因型多态性相关的膀胱癌风险

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摘要

Matrix metalloproteinases (MMPs) contribute to tumor invasion and microenvironment, hence are associated with bladder cancer risk. We therefore, tested whether polymorphisms in MMP genes modify the risk of bladder cancer (BC) and whether smoke exposure modifies this risk.Genotyping was performed in 200 BC patients and 200 controls by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). MMP1-1607 2G/2G and MMP7-181 GG genotype were associated with increased risk of BC (p <0.001; OR, 3.04; 95% CI1.71–5.39 and p, 0.005; OR, 2.38; 95% CI1.30–4.34) respectively. Smokers in BC patients showed significant increased risk for the same SNPs (p, 0.006; OR, 3.20; 95% CI1.40–7.31 and p, 0.009; OR, 2.85; 95% CI1.30–6.23 respectively). Haplotype analysis too revealed significant association with G/2G of MMP1-519-1607 (p < 0.001; OR, 2.62; 95% CI1.68–4.09). The 2G allele carrier (1G/2G + 2G/2G) of MMP1-1607 showed a protective effect and high recurrence free survival in Bacillus Calmette-Guerin (BCG) treated non muscle invasive BC (NMIBC) patients (log rank p, 0.030). Our datasuggested that MMP11607 2G and MMP7181 G allele were associated with high risk of BC, which was quite evident amongst smokers too. BCG treated NMIBC patients reflected protective effect for 2G allele carrier (1G/2G+2G/2G) of MMP1-1607. This study provided new support for the association of MMP1-1607 and MMP7-181 in bladder cancer development, the tumorigenic effect of which was observed to be more enhanced in case of tobacco exposure.
机译:基质金属蛋白酶(MMP)有助于肿瘤浸润和微环境,因此与膀胱癌风险相关。因此,我们测试了MMP基因中的多态性是否会改变膀胱癌(BC)的风险以及烟雾暴露是否会改变这种风险。通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)在200例BC患者和200例对照中进行了基因分型。 。 MMP1-1607 2G / 2G和MMP7-181 GG基因型与BC风险增加相关(p <0.001; OR,3.04; 95%CI1.71-5.39和p,0.005; OR,2.38; 95%CI1.30- 4.34)。卑诗省吸烟者表现出相同SNP的风险显着增加(p,0.006; OR,3.20; 95%CI1.40–7.31和p,0.009; OR,2.85; 95%CI1.30–6.23)。单倍型分析也显示与MMP1-519-1607的G / 2G显着相关(p <0.001; OR,2.62; 95%CI1.68–4.09)。 MMP1-1607的2G等位基因载体(1G / 2G + 2G / 2G)在芽孢杆菌(Calmet Calmette-Guerin)(BCG)治疗的非肌肉浸润性BC(NMIBC)患者中显示出保护作用和高无复发生存率(对数等级p,0.030) 。我们的数据表明,MMP11607 2G和MMP7181 G等位基因与BC高风险相关,这在吸烟者中也很明显。 BCG治疗的NMIBC患者反映了对MMP1-1607的2G等位基因携带者(1G / 2G + 2G / 2G)的保护作用。这项研究为MMP1-1607和MMP7-181与膀胱癌发展之间的联系提供了新的支持,据观察,在暴露于烟草的情况下,其致癌作用更加增强。

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