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rs11615、rs2276466、rs2228000和rs2228001基因多态性增加了孟加拉人群患宫颈癌的风险和侵袭性。

The rs11615, rs2276466, rs2228000 and rs2228001 polymorphisms increase the cervical cancer risk and aggressiveness in the Bangladeshi population.

作者信息

Das Shiba, Naher Lutfur, Aka Tutun Das, Aziz Md Abdul, Shabnaz Samia, Shahriar Mohammad, Islam Mohammad Safiqul

机构信息

Department of Pharmacy, University of Asia Pacific, Dhaka 1205, Bangladesh.

Department of Pharmacy, Noakhali Science and Technology University, Sonapur, Noakhali 3814, Bangladesh.

出版信息

Heliyon. 2021 Jan 9;7(1):e05919. doi: 10.1016/j.heliyon.2021.e05919. eCollection 2021 Jan.

Abstract

BACKGROUND

Multiple studies around the world revealed that genetic polymorphism in different genes of the DNA repair system might affect the DNA repair capabilities and accelerate the chances of cervical cancer (CC) development. Therefore, we aimed to evaluate the association of DNA repair gene- rs11615, rs2276466, rs2228000 and rs2228001 polymorphisms and CC susceptibility in the Bangladeshi population.

METHODS

A case-control genetic association study was conducted among 210 patients with diagnostically confirmed CC and 200 healthy volunteers. The -value and OR (odds ratios) with 95% CI (confidence interval) were evaluated to get the level of association.

RESULTS

After the individual analysis of all SNPs, we noticed that rs11615 possessed a significantly lower risk, whereas rs2276466 possessed a significantly elevated risk of CC in all genetic models ( < 0.05). rs2228000 showed a significantly lower risk of CC in TC, TC + CC genotypes and allele model (OR = 0.61, = 0.025; OR = 0.61, = 0.019 and OR = 0.67, = 0.027, respectively), whereas rs2228001 possessed a significantly elevated risk of CC in CA, CA + AA genotypes and allele model (OR = 1.67, = 0.012; OR = 1.69, = 0.009 and OR = 1.42, = 0.022). Besides, rs2276466 (Grade III vs. I + II: OR = 4.01, = 0.003) and rs2228001 (Grade III vs. I + II: OR = 3.38, = 0.003) were connected with high tumor aggressiveness and rs2276466 was also showed a lower risk of CC development in the younger population (<45 years).

CONCLUSION

The findings supported that rs2276466 and rs2228001 polymorphisms increase CC development and aggressiveness, whereas rs11615 and rs2228000 lower the CC risk in the studied population.

摘要

背景

世界各地的多项研究表明,DNA修复系统不同基因中的基因多态性可能会影响DNA修复能力,并增加宫颈癌(CC)发生的几率。因此,我们旨在评估DNA修复基因rs11615、rs2276466、rs2228000和rs2228001多态性与孟加拉人群中CC易感性的关联。

方法

对210例经诊断确诊为CC的患者和200名健康志愿者进行了病例对照基因关联研究。评估P值和95%置信区间(CI)的比值比(OR)以确定关联程度。

结果

在对所有单核苷酸多态性(SNP)进行个体分析后,我们注意到在所有遗传模型中,rs11615的CC风险显著降低,而rs2276466的CC风险显著升高(P<0.05)。rs2228000在TC、TC + CC基因型和等位基因模型中显示出显著较低的CC风险(OR = 0.61,P = 0.025;OR = 0.61,P = 0.019;OR = 0.67,P = 0.027),而rs2228001在CA、CA + AA基因型和等位基因模型中具有显著升高的CC风险(OR = 1.67,P = 0.012;OR = 1.69,P = 0.009;OR = 1.42,P = 0.022)。此外,rs2276466(III级与I + II级:OR = 4.01,P = 0.003)和rs2228001(III级与I + II级:OR = 3.38,P = 0.003)与高肿瘤侵袭性相关,并且rs2276466在较年轻人群(<45岁)中也显示出较低的CC发生风险。

结论

研究结果支持rs2276466和rs2228001多态性增加CC的发生和侵袭性,而rs11615和rs2228000降低了所研究人群中的CC风险。

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